Clinical Evaluation Followed by Molecular Diagnosis in a Multiplex Pedigree of Angelman Syndrome: A Case Report

Angelman syndrome (AS) is a neurodevelopmental disorder characterized by severe developmental delay or intellectual disability caused by either disruption of the maternal UBE3A gene or deletion in the maternal 15q11-q13. Diagnosis of AS in two siblings with normal four-generation history was confirm...

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Bibliographic Details
Main Authors: Azam Ahmadi Shadmehri, Fahimeh Akbarian, Jamileh Rezazadeh Varaghchi, M. Amin Tabatabaiefar
Format: Article
Language:English
Published: University of Tehran 2022-12-01
Series:Journal of Sciences, Islamic Republic of Iran
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Online Access:https://jsciences.ut.ac.ir/article_91383_0f16821d11dc13e5babd2674cb43442d.pdf
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