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...
Saved in:
| 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 |
| Subjects: | |
| Online Access: | https://jsciences.ut.ac.ir/article_91383_0f16821d11dc13e5babd2674cb43442d.pdf |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Myoclonus in Angelman Syndrome
by: J Gordon Millichap
Published: (1996-10-01) -
Epilepsy in Angelman’s Syndrome
by: J Gordon Millichap
Published: (2009-12-01) -
Neurologic and EEG Findings in Angelman Syndrome
by: J Gordon Millichap
Published: (2005-02-01) -
Exaggerated T‐wave alternans in children with Angelman syndrome
by: Eleonora Tamilia, et al.
Published: (2024-12-01) -
Angelman Syndrome without Chromosome Anomaly
by: J Gordon Millichap
Published: (1998-03-01)