Literature DB >> 22504056

Cognitive and behavioral profile in females with epilepsy with PDCH19 mutation: two novel mutations and review of the literature.

Ana Camacho1, Rogelio Simón, Raúl Sanz, Antonio Viñuela, Antonio Martínez-Salio, Fernando Mateos.   

Abstract

Mutation in the protocadherin 19 (PCDH19) gene is an increasingly recognized cause of epilepsy in females. This disorder is frequently associated with mental retardation and psychiatric features. We describe two unrelated females with novel PCDH19 missense mutations. One was de novo, and the other was inherited from her unaffected father. Both had mild mental impairment but had remarkable behavioral problems. We reviewed the cognitive and behavioral profiles of previously reported PCDH19-positive cases. Intellectual disability appeared in 75% of patients, ranging from borderline to severe. More than half of the individuals presented behavioral disturbances, which could be divided into two different groups: autistic and non-autistic. The majority of patients with autism already had some degree of cognitive impairment. It appears that seizures tend to diminish or even stop in adolescence, so non-epileptic problems can become the most important and disabling issue in adult patients with PCDH19 mutation.
Copyright © 2012 Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 22504056     DOI: 10.1016/j.yebeh.2012.02.023

Source DB:  PubMed          Journal:  Epilepsy Behav        ISSN: 1525-5050            Impact factor:   2.937


  14 in total

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Authors:  Stacey L Peek; Kar Men Mah; Joshua A Weiner
Journal:  Cell Mol Life Sci       Date:  2017-06-19       Impact factor: 9.261

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Authors:  Hao Deng; Wen Zheng; Zhi Song
Journal:  Mol Neurobiol       Date:  2013-11-22       Impact factor: 5.590

3.  Protocadherins and the Social Brain.

Authors:  Nien-Pei Tsai; Kimberly M Huber
Journal:  Biol Psychiatry       Date:  2017-02-01       Impact factor: 13.382

4.  Clinical and genetic aspects of PCDH19-related epilepsy syndromes and the possible role of PCDH19 mutations in males with autism spectrum disorders.

Authors:  J J T van Harssel; S Weckhuysen; M J A van Kempen; K Hardies; N E Verbeek; C G F de Kovel; W B Gunning; E van Daalen; M V de Jonge; A C Jansen; R J Vermeulen; W F M Arts; H Verhelst; A Fogarasi; J F de Rijk-van Andel; A Kelemen; D Lindhout; P De Jonghe; B P C Koeleman; A Suls; E H Brilstra
Journal:  Neurogenetics       Date:  2013-01-20       Impact factor: 2.660

Review 5.  Epilepsy and mental retardation restricted to females: X-linked epileptic infantile encephalopathy of unusual inheritance.

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Journal:  J Appl Genet       Date:  2014-09-10       Impact factor: 3.240

Review 6.  Developmental brain dysfunction: revival and expansion of old concepts based on new genetic evidence.

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Authors:  Yu-Chih Lin; Jeannine A Frei; Michaela B C Kilander; Wenjuan Shen; Gene J Blatt
Journal:  Front Cell Neurosci       Date:  2016-11-17       Impact factor: 5.505

8.  Male patients affected by mosaic PCDH19 mutations: five new cases.

Authors:  I M de Lange; P Rump; R F Neuteboom; P B Augustijn; K Hodges; A I Kistemaker; O F Brouwer; G M S Mancini; H A Newman; Y J Vos; K L Helbig; C Peeters-Scholte; M Kriek; N V Knoers; D Lindhout; B P C Koeleman; M J A van Kempen; E H Brilstra
Journal:  Neurogenetics       Date:  2017-07-01       Impact factor: 2.660

9.  The female epilepsy protein PCDH19 is a new GABAAR-binding partner that regulates GABAergic transmission as well as migration and morphological maturation of hippocampal neurons.

Authors:  Silvia Bassani; Andrzej W Cwetsch; Laura Gerosa; Giulia M Serratto; Alessandra Folci; Ignacio F Hall; Michele Mazzanti; Laura Cancedda; Maria Passafaro
Journal:  Hum Mol Genet       Date:  2018-03-15       Impact factor: 6.150

10.  Regulation of Neural Circuit Development by Cadherin-11 Provides Implications for Autism.

Authors:  Jeannine A Frei; Robert F Niescier; Morgan S Bridi; Madel Durens; Jonathan E Nestor; Michaela B C Kilander; Xiaobing Yuan; Derek M Dykxhoorn; Michael W Nestor; Shiyong Huang; Gene J Blatt; Yu-Chih Lin
Journal:  eNeuro       Date:  2021-07-07
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