Literature DB >> 23169763

Developmental and behavioral characteristics of individuals with Pallister-Killian syndrome.

Anna Kostanecka1, Lindsey B Close, Kosuke Izumi, Ian D Krantz, Mary Pipan.   

Abstract

Pallister-Killian syndrome is a sporadic disorder caused by the presence of mosaic tetrasomy of the short arms of chromosome 12. Case reports of children with Pallister-Killian syndrome have described a range of developmental and behavioral outcomes, but no systematic studies of these outcomes exist. The objective of this study was to describe developmental and behavioral characteristics of individuals with Pallister-Killian syndrome participating in a national meeting of families and their affected children. Sixteen individuals with Pallister-Killian syndrome, ages 16 months to 19 years, were studied using questionnaires and direct interview. Among the 16 patients enrolled in the study, 3 probands were between 16 and 19 months, and had severe developmental delay. Among the rest of the 13 probands older than 24 months, 11 children had a developmental level of less than 8 months age equivalent. They were non-ambulatory, non-verbal, and passive, requiring extensive assistance in daily living. There were two higher functioning children who were ambulatory, and verbal. One of these children met criteria for Autism on the Autism Diagnostic Interview-Revised. Thus, although most individuals with Pallister-Killian syndrome studied showed profound intellectual disability and sensory impairments, individuals with Pallister-Killian syndrome can have mild to moderate intellectual disability. Therefore, in individuals with physical examination findings of Pallister-Killian syndrome, formal diagnostic testing should be considered, even in individuals with mild to moderate intellectual disability. Further studies will be needed to determine if these higher functioning children with Pallister-Killian syndrome are at increased risk for autism.
Copyright © 2012 Wiley Periodicals, Inc.

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Year:  2012        PMID: 23169763     DOI: 10.1002/ajmg.a.35670

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  12 in total

1.  Seizures and Cardiomyopathy in a Patient with Pallister-Killian Syndrome due to Hexasomy 12p Mosaicism.

Authors:  Reha M Toydemir; Emanuele Panza; Maria C Longhurst; Sarah T South; Alan F Rope
Journal:  Mol Syndromol       Date:  2020-04-10

2.  TeratoScore: Assessing the Differentiation Potential of Human Pluripotent Stem Cells by Quantitative Expression Analysis of Teratomas.

Authors:  Yishai Avior; Juan Carlos Biancotti; Nissim Benvenisty
Journal:  Stem Cell Reports       Date:  2015-06-09       Impact factor: 7.765

3.  Cytogenomic delineation and clinical follow-up of 10 Brazilian patients with Pallister-Killian syndrome.

Authors:  Larissa Sampaio de Athayde Costa; Aline C Zandona-Teixeira; Marilia M Montenegro; Alexandre T Dias; Roberta L Dutra; Rachel S Honjo; Debora R Bertola; Leslie D Kulikowski; Chong A Kim
Journal:  Mol Cytogenet       Date:  2015-06-26       Impact factor: 2.009

4.  Sleep in Children With Pallister Killian Syndrome: A Prospective Clinical and Videopolysomnographic Study.

Authors:  Anna Fetta; Veronica Di Pisa; Martina Ruscelli; Luca Soliani; Giacomo Sperti; Sara Ubertiello; Emilia Ricci; Greta Mainieri; Alessandro Rocca; Maria Margherita Mancardi; Lucio Giordano; Dario Pruna; Aglaia Vignoli; Federica Provini; Duccio Maria Cordelli
Journal:  Front Neurol       Date:  2021-12-16       Impact factor: 4.003

5.  Cognitive, Behavioral, and Sensory Profile of Pallister-Killian Syndrome: A Prospective Study of 22 Individuals.

Authors:  Anna Fetta; Luca Soliani; Alessia Trevisan; Rosa Pugliano; Emilia Ricci; Veronica Di Pisa; Veronica Pignataro; Marida Angotti; Alessandro Rocca; Bianca Salce; Maria Margherita Mancardi; Lucio Giordano; Dario Pruna; Antonia Parmeggiani; Duccio Maria Cordelli
Journal:  Genes (Basel)       Date:  2022-02-16       Impact factor: 4.096

6.  Mosaic epigenetic dysregulation of ectodermal cells in autism spectrum disorder.

Authors:  Esther R Berko; Masako Suzuki; Faygel Beren; Christophe Lemetre; Christine M Alaimo; R Brent Calder; Karen Ballaban-Gil; Batya Gounder; Kaylee Kampf; Jill Kirschen; Shahina B Maqbool; Zeineen Momin; David M Reynolds; Natalie Russo; Lisa Shulman; Edyta Stasiek; Jessica Tozour; Maria Valicenti-McDermott; Shenglong Wang; Brett S Abrahams; Joseph Hargitai; Dov Inbar; Zhengdong Zhang; Joseph D Buxbaum; Sophie Molholm; John J Foxe; Robert W Marion; Adam Auton; John M Greally
Journal:  PLoS Genet       Date:  2014-05-29       Impact factor: 5.917

7.  Dental Treatment of a Child with Pallister-Killian Syndrome.

Authors:  Serhan Didinen; Didem Atabek; Gülay Kip; Aslı Patır Münevveroğlu; Özlem Tulunoğlu
Journal:  Case Rep Dent       Date:  2016-02-21

8.  Detecting, quantifying, and discriminating the mechanism of mosaic chromosomal aneuploidies using MAD-seq.

Authors:  Yu Kong; Esther R Berko; Anthony Marcketta; Shahina B Maqbool; Claudia A Simões-Pires; David F Kronn; Kenny Q Ye; Masako Suzuki; Adam Auton; John M Greally
Journal:  Genome Res       Date:  2018-05-17       Impact factor: 9.043

9.  Prenatal diagnosis of Pallister-Killian syndrome in one twin.

Authors:  Lin Li; Linhuan Huang; Xuan Huang; Shaobin Lin; Zhiming He; Qun Fang
Journal:  Clin Case Rep       Date:  2018-06-13

10.  Pallister-Killian syndrome: clinical, cytogenetic and molecular findings in 15 cases.

Authors:  Birsen Karaman; Hülya Kayserili; Asadollah Ghanbari; Zehra Oya Uyguner; Güven Toksoy; Umut Altunoglu; Seher Basaran
Journal:  Mol Cytogenet       Date:  2018-08-17       Impact factor: 2.009

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