Epilepsy is a possible feature in Williams-Beuren syndrome patients harboring typical deletions of the 7q11.23 critical region-Reference-Cited by-同舟云学术

Epilepsy is a possible feature in Williams-Beuren syndrome patients harboring typical deletions of the 7q11.23 critical region

Published:2015-10-05 Issue:1 Volume:170 Page:148-155
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Nicita Francesco¹,Garone Giacomo¹,Spalice Alberto¹,Savasta Salvatore²,Striano Pasquale³,Pantaleoni Chiara⁴,Spartà Maria Valentina²,Kluger Gerhard⁵,Capovilla Giuseppe⁶,Pruna Dario⁷,Freri Elena⁴,D'Arrigo Stefano⁴,Verrotti Alberto⁸

Affiliation:

1. Child Neurology Division; Department of Pediatrics; Umberto I Hospital; Sapienza University; Roma Italy

2. Department of Pediatrics; University of Pavia; IRCCS Policlinico San Matteo; Pavia Italy

3. Pediatric Neurology and Muscular Diseases Unit; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa; 'G. Gaslini' Institute; Italy

4. Department of Pediatric Neuroscience; Foundation I.R.C.C.S. Neurological Institute “C. Besta”; Milan Italy

5. Sch; ö; n Klinik Vogtareuth; Hospital for Neuropediatrics and Neurological Rehabilitation; Epilepsy Center for Children and Adolescents; Vogtareuth Germany

6. Epilepsy Center; Department of Child Neuropsychiatry; C Poma Hospital; Mantova Italy

7. Epilepsy Unit, Child Neuropsychiatry Department; University Hospital; Cagliari Italy

8. Department of Pediatrics; University of Perugia; Perugia Italy

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference23 articles.

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2. Periventricular nodular heterotopia and Williams syndrome;Ferland;Am J Med Genet A,2006

3. Smaller and larger deletions of the Williams Beuren syndrome region implicate genes involved in mild facial phenotype, epilepsy and autistic traits;Fusco;Eur J Hum Genet,2014

4. Increased local gyrification mapped in Williams syndrome;Gaser;Neuroimage,2006

5. Microscopically visible deletion of chromosome 7 in a child with features of Williams syndrome;Kahler;Am J Hum Genet,1995

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