Angelman Syndrome is a Rare Neurogenetic Disorder

Abstract Angelman syndrome is a genetic disorder that causes formative delays and neurological issues – challenges with discourse, adjust and strolling, and in some cases, epileptic seizures. It is caused by a transformation in chromosome 15 acquired from the mother. It is named after Dr. Harry Angelman, a British pediatrician who to begin with depicted the syndrome in 1965. Angelman syndrome is ordinarily not found until guardians start to take note formative delays when the child is between 6 and 12 months old. Keywords: AS, Genes, Imbalances, Behavior, Health

Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2025-02-22
DOI
https://doi.org/10.5281/zenodo.14917032
Primary Topic
Genetic Syndromes and Imprinting
Type
article
Field-Weighted Citation Impact
0.00
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article

Angelman Syndrome is a Rare Neurogenetic Disorder

Zenodo (CERN European Organization for Nuclear Research)
Genetic Syndromes and Imprinting
article

Angelman Syndrome is a Rare Neurogenetic Disorder

article en

Abstract

Abstract Angelman syndrome is a genetic disorder that causes formative delays and neurological issues – challenges with discourse, adjust and strolling, and in some cases, epileptic seizures. It is caused by a transformation in chromosome 15 acquired from the mother. It is named after Dr. Harry Angelman, a British pediatrician who to begin with depicted the syndrome in 1965. Angelman syndrome is ordinarily not found until guardians start to take note formative delays when the child is between 6 and 12 months old. Keywords: AS, Genes, Imbalances, Behavior, Health

Zenodo (CERN European Organization for Nuclear Research)
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Genetic Syndromes and Imprinting
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Angelman Syndrome is a Rare Neurogenetic Disorder · Zenodo (CERN European Organization for Nuclear Research) (2025) | TGRS Research Map | TGRS