Safety Data Sheet according to Regulation (EC) No. 1907/2006 (REACH)Printed Contact VA250black, VA2500HT (GB) 1. IDENTIFICATION OF THE SUBSTANCE/PREPARATION AND OF THE COMPANY/UNDERTAKING Name of product Contact VA250black, VA2500HT (GB)Code-Nr. 12-4 Manufacturer/distributor WEICON GmbH & Co. KGKönigsberger Straße 255, DE-48157 MünsterPostboxPhone ++49(0)251 / 9322 - 0, Fax +
American people can buy antibiotics in Australia online here: https://buyantibiotics-24h.com/ No prescription required and cheap price!
Seizure characteristics in pallisterkillian syndromeSeizure Characteristics in Pallister–Killian SyndromeMeghan S. Candee,1* John C. Carey,2 Ian D. Krantz,3 and Francis M. Filloux11Division of Pediatric Neurology, Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, Utah2Division of Medical Genetics, Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, Utah; Intermountain Healthcare,Salt Lake City, Utah3Division of Human Genetics, The Children’s Hospital of Philadelphia and the Perelman School of Medicine at the University of Pennsylvania,Philadelphia, Pennsylvania Manuscript Received: 11 February 2012; Manuscript Accepted: 18 June 2012 Pallister–Killian syndrome (PKS) is a congenital disorder attrib-uted to supernumerary isochromosome 12p mosaicism. Cranio- facial dysmorphism, learning impairment and seizures are Candee MS, Carey JC, Krantz ID, Filloux. FM.
considered cardinal features. However, little is known regarding the seizure and epilepsy patterns in PKS. To better deﬁne the prevalence and spectrum of seizures in PKS, we studied 51 patients (39 male, 12 female; median age 4 years and 9 months;age range 7 months to 31 years) with conﬁrmed 12p tetrasomy.
Using a parent-based structured questionnaire, we collected dataregarding seizure onset, frequency, timing, semiology, and med- frequently identiﬁed in cells cultured from skin ﬁbroblasts or buccal ication therapy. Patients were recruited through our practice, at mucosa [Bielanska et al., 1996]. Given the mosaic nature of the PKS Kids family events, and via the PKS Kids website. Epilepsy condition, genetic diagnosis is often elusive as karyotypes per- occurred in 27 (53%) with 23 (85%) of those with seizures having formed only on blood cells may fail to identify the condition seizure onset prior to 3.5 years of age. Mean age at seizure onset [Horneff et al., 1993; Bielanska et al., 1996]. The PKS phenotype was 2 years and 4 months. The most common seizure types were is typically described by the presence of three general ﬁndings: myoclonic (15/27, 56%), generalized convulsions (13/27, 48%), craniofacial dysmorphism, cognitive impairment [Stalker et al., and clustered tonic spasms (similar to infantile spasms; 8/27, 2006] (ranging from moderate to severe intellectual disability), and 30%). Thirteen of 27 patients with seizures (48%) had more than one seizure type with 26 out of 27 (96%) ever having taken The majority of existing literature on PKS has focused on antiepileptic medications. Nineteen of 27 (70%) continued to reafﬁrming the craniofacial dysmorphisms (e.g., forehead promi- have seizures and 17/27 (63%) remained on antiepileptic medi- nence, temporal balding, and hypertelorism as shown in Fig. 1), cation. The most commonly used medications were: levetirace- associated congenital defects (e.g., diaphragmatic hernia, cleft tam (10/27, 37%), valproic acid (10/27, 37%), and topiramate palate, heart anomalies, etc.), physical exam ﬁndings (e.g., hypoto- (9/27, 33%) with levetiracetam felt to be ‘‘most helpful’’ by nia and anomalous skin pigmentation) and genotypic variations parents (6/27, 22%). Further exploration of seizure timing, observed [Smigiel et al., 2008]. Thus far, there does not appear to be in-depth analysis of EEG recordings, and collection of MRI a correlation between the proportion of tetrasomic cells and the data to rule out confounding factors is warranted.
severity of a patient’s clinical presentation (i.e., severity of congeni- tal abnormalities, survival, and degree of cognitive impairment)[Schinzel, 1991; Speleman et al., 1991]. Exploration of the critical Key words: Pallister; Killian; seizures; epilepsy; 12p; tetrasomy gene region of i12p responsible for PKS is ongoing.
In contrast to what is known about the epilepsy characteristics of other chromosomal disorders (e.g., Angelman [Minassian et al.,1998], Wolf–Hirschhorn (4pÀ) [Battaglia et al., 2009], inverted duplication 15 [Battaglia et al., 1997], terminal deletion 1p36 Pallister–Killian syndrome (PKS), also known as Pallister mosaic aneuploidy syndrome [Reynolds et al., 1987], is a rare sporadic Meghan S. Candee, Division of Pediatric Neurology, Department of disorder ﬁrst described in adults in 1977 by Pallister [Pallister et al., Pediatrics, Primary Children’s Medical Center, 100 N. Mario Capecchi 1977] and in children in 1981 by Killian and Teschler-Nicola Drive, Salt Lake City, UT 84113. E-mail: email@example.com . PKS is caused by the presence of a supernumerary isochro- Article ﬁrst published online in Wiley Online Library mosome (i12p) which confers tetrasomy. The chromosomal anom- aly is often absent in peripheral blood lymphocytes but is more AMERICAN JOURNAL OF MEDICAL GENETICS PART A children had onset of clustered epileptic spasms after infancy(‘‘late-onset spasms’’) and one of these children had an EEGconsistent with ‘‘modiﬁed hypsarrhythmia.’’ Of these four chil-dren, one had onset of ‘‘massive myoclonic jerks’’ at age 13 monthsthat appeared photosensitive in nature, and clustered tonic spasmsonly emerged later at age 4 [Cerminara et al., 2010]. The last of theseﬁve children had onset of partial clonic seizures at age 5.5 yearsfollowed by the appearance of clustered tonic spasms in ﬂexion1 year later [Cerminara et al., 2010]. This prior data, though basedon a very small sample size, would suggest that children with PKScould be prone to later onset clustered spasms as a particularepileptic phenotype. Other case reports (Table I) suggest alternativeseizure semiology. For example, Smigiel et al.  reporteduncategorized seizures in a neonate with PKS, while Spelemanet al.  described two patients with generalized seizures whowere treated with valproic acid. Clearly, the existing informationavailable with respect to the seizure and epilepsy characteristics in FIG. 1. PKS patient facial characteristics. Note hypertelorism, PKS (Table I) is limited and presented in a fairly inconsistent and temporal balding, forehead prominence, and macrostomia.
fragmentary manner. This is because seizures were never before thefocus of investigation as such. Further delineation of an epilepsyphenotype (or phenotypes) in PKS may aid in seizure diagnosis, Bahi-Buisson et al., 2008a,b] and ring chromosome 20 syndromes improve anti-epileptic management, and provide a better under- [Inoue et al., 1997]), very little is known regarding the frequency of standing of prognosis for families and physicians [Battaglia et al., seizures, age of onset, typical seizure types, response to treatment or In the present paper, we describe the seizure characteristics of 51 Prior case series and meta-analyses (Table I) suggest seizure patients with PKS, the largest cohort of such patients to be evaluated prevalence in PKS to be in the vicinity of 42–59% [Bielanska et al., for seizures and epilepsy to date. This was made possible via web- 1996; Stalker et al., 2006]. However, these numbers are rough based contact and alliance with the family support group for people estimates, not to be mistaken for careful analysis of a particular affected by Pallister–Killian syndrome [http://pkskids.net/].
To date, only three groups (Table I) have described the detailed semiology and clinical characteristics of epileptic seizures in atotal of ﬁve children with PKS [Sanchez-Carpintero et al., 2005; Fifty-one patients with a diagnosis of Pallister–Killian syndrome Yamamoto et al., 2007; Cerminara et al., 2010]. Four of these (39 males and 12 females), as conﬁrmed by parent-reported chro- TABLE I. Pallister–Killian Syndrome Seizure Literature Review—Comparison between Previously Reported Pallister–Killian Syndrome Neonatal–4 y Staring spells Æ quick head jerks, Myoclonic, partial, ﬂex/extensor spasms Mean 2 y 4 m Myoclonic, generalized, infantile spasm, y, years; m, months; NR, not reported; CBZ, carbamazepine; CLB, clobazam; CNZ, clonazepam; DPH, diphenylhydantoin; ESM, thosuximide; LEV, levetiracetam; LTG, lamotrigine; OCBZ, oxcarbazepine;PHB, phenobarbitol; TPM, topiramate; VGB, vigabatrin; VPA, valproic acid; Vit B6, vitamin B6.
mosomal analysis, were included. Patients were identiﬁed initially Informed consent was obtained as the study involved voluntary via clinical contact, attendance at PKS support group meetings provision of personal medical information and requested the or by contact via notiﬁcations on the PKS Kids family web site option (which patients could refuse) of future contact by the investigators. The study was reviewed and approved by theInstitutional Review Board of the University of Utah in Salt LakeCity, UT.
Inclusion Criteria1. Any patient presenting (or having presented within the past 20 years) to the pediatric neurology or pediatric genetics divi- sions at University of Utah Medical Center/Primary Children’sMedical Center with a diagnosis of Pallister–Killian syndrome The parents of 51 children with a conﬁrmed diagnosis of PKS was offered participation. In addition, patients/parents involved completed our survey. The median age of all patients at the time of in the international PKS Kids organization, families of patients study was 4 years and 9 months with a range of 7 months to 31 years visiting the PKS Kids web site, and families attending the (Table II). Seizures/epilepsy affected 27 of the 51 patients (53%).
2009 or 2010 annual PKS Kids Family meetings were offered Amongst patients diagnosed with seizures, the mean age was 8 years and 4 months, with a range of 19 months to 31 years 2. Parent-reported genetic diagnosis of PKS (i.e., mosaic tetrasomy (Table III). An additional 10% of parents suspected that their 12p as conﬁrmed by ﬂuorescence in situ hybridization, in child had seizures (Fig. 2). Taken together, 63% of patients ﬁbroblast culture, or other tissue).
in our cohort were identiﬁed as having conﬁrmed or suspectedseizures.
More than half of the patients diagnosed with seizures (56%) had seizure onset by 2 years of age, and nearly all of the patients withseizures (96%) had onset by 6 years (Fig. 3). The majority of Patients (and their families) were excluded if the diagnosis of PKS the patients (63%) had seizures during both the day and night.
had not yet been conﬁrmed by chromosomal analysis (i.e., if their Twenty-two percent of parents reported that their child had ever diagnosis was suspected purely based on clinical presentation).
experienced status epilepticus. The most common seizure types Clinical details were obtained through a parent-based structured noted in our cohort of children with PKS were (in decreasing order questionnaire which was handed, mailed, or emailed to parents of frequency, as shown in Fig. 4) myoclonic (15/27, 56%), general- of children with PKS. The questionnaire included (but was not ized convulsive (13/27, 48%), clustered tonic spasms (i.e., ‘‘infantile’’ spasms though usually occurring beyond infancy; 8/27, 30%), brief staring episodes (5/27, 19%), and complex partial seizures (3/27, 11%). Only one of the eight patients with clustered tonic spasms (‘‘infantile spasms’’) had spasm onset prior to 2 years * Seizure type, frequency, timing (day/night/both), dura- of age. Nearly half of patients with seizures (13/27, 48%) had more Ninety-six percent of patients with seizures had ever taken antiepileptic medication with 56% having tried two or more (Table III). Sixty-three percent of patients with seizures remained on antiepileptic medication at the time of study. The most frequently used medications were valproic acid (10/27, 37%), levetiracetam (10/27, 37%), topiramate (9/27, 33%), phenobarbital(6/27, 22%), and lamotrigine (6/27, 22%; Fig. 5). The medications Of note, precise delineation of seizure timing (e.g., while waking/ considered to be most helpful by parents were: levetiracetam (6/27, awake/falling asleep/asleep, conditions which are not mutually 22%), and phenobarbital, valproic acid, topiramate, and lamotri- exclusive in that patients can have seizures at multiple levels of alertness) was not distinctly elucidated, largely because the questionpertaining to this information was only added into a later version ofthe survey. Direct parent interviews and/or phone/email contactwith parents was employed in order to ascertain speciﬁc details notfully clariﬁed in the initially completed survey (e.g., when a question TABLE II. Selected Patient Characteristics was left blank or incomplete). Copies of pertinent medical records(e.g., EEG and MRI reports) were also requested and are still being collected at this time. As such, the EEG and MRI ﬁndings will not be discussed here. No incentives for participation were offered or Data from the collected surveys were summarized using descrip- tive statistics such as percentages, means, and standard deviations.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A TABLE III. Seizure Patient Characteristics (n ¼ 27) AEDs, antiepileptic drugs.
aLikely confounded by longer spasm clusters.
FIG. 3. Timing of seizure onset. Fifty-six, eighty-ﬁve, and ninety-sixpercent of patients with seizures had seizure onset by 2, 3.5, and 6years, respectively.
Including 51 patients with PKS, this is the largest cohort to date ofpatients with PKS to be evaluated for seizures and epilepsy. Our data Although it has been previously suggested that most of the conﬁrm that seizures are a common occurrence in children with patients with PKS who are going to develop seizures do so shortly PKS, affecting more than 50% of children by age 2 years.
after birth [Schinzel, 1991], our data suggest otherwise as only Our total of 63% of patients with conﬁrmed or suspected seizures eleven (35% or about one third) of the patients with seizures had is noticeably higher than some previously reported prevalence seizures prior to 1 year of age and neonatal seizures were only estimates (e.g., 42% noted by Bielanska et al. [1996) but quite reported in one child (2%). Likewise, our ﬁndings do support the similar to that noted by Reynolds et al.  in their case series of notion suggested in the ﬁve previously described patients [Sanchez- 10 patients and one stillborn fetus with PKS (i.e., 70%; also see Carpintero et al., 2005; Yamamoto et al., 2007; Cerminara et al., Table I). The inclusion of many very young children in our cohort 2010 also see Table I] that late onset spasms (occurring after 1 year along with the broad spectrum of seizure types diagnosed and the of age, and hence after the typical age of onset for ‘‘infantile suspicion (on behalf of parents) that their children have seizures spasms’’) may represent a relatively common epileptic pattern which are not always formally diagnosed, suggest that seizures may for children with PKS. Although 22% of parents reported that be even more common than we report here. This emphasizes the their child had ever experienced status epilepticus, based on subse- importance of following this cohort into the future as well as the quent careful review of our survey data, we believe this number to be need to expand the awareness of practitioners in looking for seizures falsely elevated secondary to parental reporting of longer clusters of tonic spasms as continuous seizure activity. Our ﬁnding that 70% FIG. 4. Common seizure types. More than half of the patients withseizures had demonstrated myoclonic seizures while nearly halfhad experienced generalized convulsions. Nearly half (48%) had FIG. 2. Seizure prevalence. Note that 63% of the patients in our PKS more than one seizure type. *Seven out of eight patients with cohort had been diagnosed or were suspected of having seizures.
‘‘infantile spasms’’ (87.5%) had onset at later than 2 years.
mal, often exhibiting a so-called ‘‘split-brain’’ pattern [Ohtsukaet al., 1993; Aicardi, 2005].
Based on the above observations, we hypothesized that children with PKS may also exhibit some predictable epilepsy or seizurepatterns. Our data so far, modestly support this hypothesis. Asreported by parents, the seizure pattern/epilepsy syndrome associ-ated with PKS is characterized by the following key elements: (1)absence of neonatal seizures; (2) onset by 2–5 years of age; (3) mixedseizure types with a predominance of myoclonic seizures and late-onset clustered tonic spasms (‘‘late-onset infantile spasms’’ withonset at greater than 1 year of age); (4) rarity of convulsive status FIG. 5. Anti-epileptic medications most frequently used and noted to epilepticus; and (5) periods of relative refractoriness.
be ‘‘most helpful.’’ While valproic acid and levetiracetam were most Although there does not appear to be a correlation between the commonly used, levetiracetam was identiﬁed as the most proportion of tetrasomic cells and the severity of a patient’s clinical presentation, further examination of the scope of seizure severitywithin this population, when combined with genetic analysis, mayshed light on the neurophysiologic mechanism of seizures in PKS. Alonger term goal of our research is to identify optimal management (19/27) of our patients with seizures continued to have seizures strategies for the treatment of seizures in PKS. While we have despite 63% (17/27) remaining on anti-epileptic medication dem- limited information in this respect thus far, it appears that the onstrates a presumed medication-refractory nature of seizures in majority of children diagnosed with seizures have required a trial of PKS. In the absence of long term follow-up data, it is not possible to more than one AED. Though levetiracetam has been identiﬁed by propose a single medication or speciﬁc regimen likely to be most parents as the most commonly effective single agent in this cohort, it effective for all or a majority of PKS children.
is by no means consistently effective. No other AED stands out as the Unfortunately, the relatively young age of many of our patients obvious second choice (see also Gerstner et al., 2008 for description limits our ability to accurately assess long-term prognosis in of valproate-associated encephalopathy in a child with PKS). Only children with PKS. However, it is interesting to note that the two patients in our cohort have required or been treated with the two oldest patients studied (now aged 29 and 31 years) are currently ketogenic diet. None had undergone vagal nerve stimulator im- seizure free. One of these two adults with PKS also appears to be one plantation. The latter two observations may speak to the relative of the ‘‘higher-functioning’’ individuals in our cohort.
lesser severity of the seizure phenotype in these children. Although Epilepsy is a common symptom of many congenital and/or our data do not yet allow us to ﬁrmly describe the long-term genetic syndromes that affect the nervous system. Some of these epilepsy prognosis of these patients, they do suggest that the overall are associated with speciﬁc epilepsy or electroencephalographic severity of epilepsy in this population is relatively less than for patterns [Battaglia et al., 1997, 2009; Inoue et al., 1997; Minassian children with Aicardi syndrome, or with other epileptic encepha- et al., 1998; Bahi-Buisson et al., 2008a,b]. For example, epilepsy is lopathies of childhood (such as Lennox–Gastaut syndrome, Myo- very common in children with Angelman syndrome and Wolf– clonic Astatic Epilepsy, or Dravet syndrome). The potential for Hirschhorn syndromes but differs substantially between the two. In remission may be less than that observed in Wolf–Hirschhorn the former, children often have mixed seizure types with frequent syndrome, but better than for girls with Rett syndrome and drop attacks and atypical absence seizures, accompanied by a certainly those with Aicardi syndrome.
characteristic EEG pattern described as periodic, large amplitude, Our survey-based study results are inherently limited by expec- slow spike-wave discharges often occurring in prolonged clusters or tation, recall and selection bias. Parents are not clinically trained trains [Minassian et al., 1998; Korff et al., 2005; Valente et al., 2006; to diagnose seizure activity and may over/under-report episodes.
Conant et al., 2009; Thibert et al., 2009]. A fair percentage of these In addition, parents with a child with epilepsy were likely more children will eventually go into remission [Uemura et al., 2005; motivated to ﬁll out this questionnaire. Considerable variability Valente et al., 2006; Thibert et al., 2009]. In contrast, more than 90% with respect to parental interpretation of questions and terms was of children with Wolf–Hirschhorn syndrome have epilepsy, but noted as well. For example, some parents could describe a seizure most have generalized tonic–clonic seizures and about half suffer but not identify the category of seizure type. The differentiation episodes of status epilepticus. However, the majority eventually between the duration of a single seizure versus a cluster of seizures experience full seizure control or remission in childhood was not always entirely clear. We have tried and intend to continue [Worthington et al., 2008; Battaglia et al., 2009]. Girls with Rett to address such potential obstacles by conducting a thorough syndrome have a mixture of seizure types, but, perhaps similar to medical record review down the road. That being said, a children with PKS, also have a variety of non-epileptic paroxysmal questionnaire-driven approach is particularly helpful in the case events which can confound management [Laan et al., 1998; Moser of rare diseases for which ascertainment of cohorts of substantial et al., 2007; Bahi-Buisson et al., 2008a,b; Buoni et al., 2008]. Finally, size is challenging [Bahi-Buisson et al., 2008a,b; Battaglia et al., girls with Aicardi syndrome, experience early onset infantile spasms 2009; Thibert et al., 2009; Cardoza et al., 2011].
and typically suffer from lifelong, severe intractable epilepsy In the future, a modiﬁed, more comprehensive survey aimed at [Ohtsuka et al., 1993; Aicardi, 2005]. EEG patterns are very abnor- capturing additional details pertaining to seizure timing and to AMERICAN JOURNAL OF MEDICAL GENETICS PART A paroxysmal behaviors noted during sleep may be beneﬁcial. An Conant KD, Thibert RL, Thiele EA. 2009. Epilepsy and the sleep-wake updated survey might also include questions regarding family patterns found in Angelman syndrome. Epilepsia 50:2497–2500.
history of epileptic seizures in order to remove this as a possible Gerstner T, Bell N, Koenig SA. 2008. Valproate-associated reversible encephalopathy in a 3-year-old girl with Pallister–Killian syndrome.
An improved understanding of the epileptic patterns and seizure types associated with PKS, of their response to treatment and Horneff G, Majewski F, Hildebrand B, Voit T, Lenard HG. 1993. Pallister– of their prognosis may provide the following beneﬁts for patients Killian syndrome in older children and adolescents. Pediatr Neurol 9: with PKS and their families: (1) earlier recognition of seizures and seizure-like spells; (2) enhanced recognition of non-epileptic Inoue Y, Fujiwara T, Matsuda KS, Kubota H, Tanaka M, Yagi K. 1997. Ring paroxysmal phenomena; (3) better prognostication; and (4) chromosome 20 and nonconvulsive status epilepticus. A new epilepticsyndrome. Brain 120:939–953.
improved anticipatory guidance. Future correlation of seizureoccurrence and pattern with genotype may help elucidate the Killian W, Teschler-Nicola M. 1981. Case report 72: Mental retardation, neurophysiological underpinnings of epilepsy in PKS patients unusual facial appearance, abnormal hair. Synd Ident 7:6–7.
and could lead towards improved medical therapy. Finally, Knab J, Heupel EW, Steinmann D. 2008. Anesthesia for orthopedic surgery long term follow-up of the present cohort and in depth analysis in Pallister–Killian syndrome. Pediatr Anesth 18:682–684.
of both EEG recordings (to conﬁrm seizure types) and MRI data Korff CM, Kelley KR, Nordli DR Jr. 2005. Notched delta, phenotype, (to characterize common anatomical variations) will be essential and Angelman syndrome. J Clin Neurophysiol 22:238–243.
to better clariﬁcation of prognosis over time.
Laan LA, Brouwer OF, Begeer CH, Zwinderman AH, van Dijk JG. 1998. The diagnostic value of the EEG in Angelman and Rett syndrome at a youngage. Electroencephalogr Clin Neurophysiol 106:404–408.
Minassian BA, DeLorey TM, Olsen RW, Philippart M, Bronstein Y, Zhang We are grateful to the PKS Kids Organization for their support and Q, Guerrini R, Van Ness P, Livet MO, Delgado-Escueta AV. 1998.
Angelman syndrome: Correlations between epilepsy phenotypes andgenotypes. Ann Neurol 43:485–493.
Moser SJ, Weber P, L€utschg J. 2007. Rett syndrome: Clinical and electro- physiologic aspects. Pediatr Neurol 36:95–100.
Ohtsuka Y, Oka E, Terasaki T, Ohtahara S. 1993. Aicardi syndrome: A Aicardi J. 2005. Aicardi syndrome. Brain Dev 27:164–171.
longitudinal clinical and electroencephalographic study. Epilepsia 34: Bahi-Buisson N, Guellec I, Nabbout R, Guet A, Nguyen G, Dulac O, Chiron C. 2008a. Parental view of epilepsy in Rett syndrome. Brain Dev 30: Pallister PD, Meisner LF, Elejalde BR, Francke U, Hermann J, Spranger J, Tiddy W, inhorn SL, Opitz JM. 1977. The Pallister mosaic syndrome.
Bahi-Buisson N, Guttierrez-Delicado E, Soufﬂet C, Rio M, Daire VC, Birth Defects Orig Art Ser 13:103–110.
Lacombe D, Heron D, Verloes A, Zuberi S, Burglen L, et al. 2008b.
Reynolds JF, Daniel A, Kelly TE, Gollin SM, Stephan MJ, Carey J, Adkins Spectrum of epilepsy in terminal 1p36 deletion syndrome. Epilepsia WN, Webb MJ, Char F, Jimenez JF, et al. 1987. Isochromosome 12p mosaicism (Pallister mosaic aneuploidy or Pallister–Killian syndrome): Battaglia A, Gurrieri F, Bertini E, Bellacosa A, Pomponi MG, Paravatou- Report of 11 cases. Am J Med Genet 27:257–274.
Petsotas M, Mazza S, Neri G. 1997. The inv dup(15) syndrome: A Sanchez-Carpintero R, McLellan A, Parmeggiani L, Cockwell AE, Ellis RJ, clinically recognizable syndrome with altered behavior, mental retarda- Cross JH, Eckhardt S, Guerrini R. 2005. Pallister–Killian syndrome: An tion, and epilepsy. Neurology 48:1081–1086.
unusual cause of epileptic spasms. Dev Med Child Neurol 47:776–779.
Battaglia A, Filippia T, South ST, Carey JC. 2009. Spectrum of epilepsy and Schinzel A. 1991. Tetrasomy 12p (Pallister–Killian syndrome). J Med Genet electroencephalogram patterns in Wolf–Hirschhorn syndrome: Experi- ence with 87 patients. Dev Med Child Neurol 51:373–380.
Smigiel R, Pilch J, Makowsa I, Buska H, Slezak R, Sasiadek MM. 2008. The Bielanska MM, Khalifa MM, Duncan MV. 1996. Pallister–Killian syn- Pallister–Killian syndrome in a child with rare karyotype—A diagnostic drome: A Mild case diagnosed by ﬂuorescene In Situ hybridization.
problem. Eur J Pediatr 167:1063–1065.
Review of the literature and expansion of the phenotype. Am J Med Genet65:104–108.
Speleman F, Leroy JG, Van Roy N, De Paepe A, Suijkerbuijk R, Brunner H, Looijenga L, Verschraegen-Spae MR, Orye E. 1991. Pallister–Killian Buoni S, Zannolli R, Felice CD, Saponari S, Strambi M, Dotti MT, Castrucci syndrome: Characterization of the isochromosome 12p by ﬂuorescent E, Corbini L, Orsi A, Hayek J. 2008. Drug-resistant epilepsy and epileptic in situ hybridization. Am J Med Genet 41:381–387.
phenotype-EEG association in MECP2 mutated Rett syndrome. ClinNeurophysiol 119:2455–2458.
Stalker HJ, Gray BA, Bent-Williams A, Zori RT. 2006. High cognitive functioning and behavioral phenotype in Pallister–Killian syndrome.
Cardoza G, Clarke A, Wilcox J, Gibbon F, Smith PE, Archer H, Am J Med Genet Part A 140A:1950–1954.
Hryniewiecka-Jaworska A, Kerr M. 2011. Epilepsy in Rett syndrome:Association between phenotype and genotype, and implications for Thibert RL, Conant KD, Braun EK, Bruno P, Said RR, Nespeca MP, Thiele EA. 2009. Epilepsy in Angelman syndrome: A questionnaire-based assessment of the natural history and current treatment options.
Cerminara C, Compagnone E, Bagnolo V, Galasso C, Lo-Castro A, Brinciotti M, Curatolo P. 2010. Late-onset epileptic spasms in childrenwith pallister-killian syndrome: A report of two new cases and review of Uemura N, Matsumoto A, Nakamura M, Watanabe K, Negoro T, Kumagai the electroclinical aspects. J Child Neurol 25:238–245.
T, Miura K, Ohki T, Mizuno S, Okumura A, et al. 2005. Evolution of seizures and electroencephalographical ﬁndings in 23 cases of deletion Worthington JC, Rigby AS, Quarrell OW. 2008. Seizure frequency in type Angelman syndrome. Brain Dev 27:383–388.
adults with Wolf–Hirschhorn syndrome. Am J Med Genet Part A146A:2528–2531.
Valente KD, Koiffmann CP, Fridman C, Varella M, Kok F, Andrade JQ, Grossmann RM, Marques-Dias MJ. 2006. Epilepsy in patients with Yamamoto H, Fukuda M, Murakami H, Kamiyama N, Miyamoto Y. 2007.
angelman syndrome caused by deletion of the chromosome 15q11– A case of Pallister–Killian syndrome associated with West syndrome.
Aneela Darbar, M.D. Assistant Professor of Neurological Surgery Areas of Interest: Cerebrovascular and Skull Base Surgery, Neuro-endoscopy Department of Neurological Surgery Saint Louis University School of Medicine EDUCATION 2008-2009 Fellowship in Minimally Invasive Cranial Neurosurgery with Dr. Charles Teo, Sydney, Australia. 2002 – 2008 Residency in Department of Neurosu