A further case of a Prader-Willi syndrome phenotype in a patient with Angelman syndrome molecular defect

A further case of a Prader-Willi syndrome phenotype in a patient with Angelman syndrome molecular defect

Angelman syndrome (AS) and Prader-Willi syndrome (PWS) are distinct human neurogenetic disorders; however, a clinical overlap between AS and PWS has been identified. We report on a further case of a patient showing the PWS phenotype with the AS molecular defect. Despite the PWS phenotype, the DNA me...

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Bibliographic Details
Main Authors: De Molfetta Greice Andreotti, Felix Temis Maria, Riegel Mariluce, Ferraz Victor Evangelista de Faria, Pina Neto João Monteiro de
Format: Article
Language:English
Published: Thieme Revinter Publicações 2002-01-01
Series:Arquivos de Neuro-Psiquiatria
Subjects:
Angelman syndrome
Prader-Willi syndrome
imprinting defect
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2002000600024
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