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Angelman Syndrome is a Rare Neurogenetic Disorder

Year: 2025

Type: article

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

Source: Zenodo (CERN European Organization for Nuclear Research)

DOI: 10.5281/zenodo.14917032

Author: Siniša Franjić

Language: English

Topic: Genetic Syndromes and Imprinting

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

Open Access status: green

OpenAlex ID: W6893196333

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