ATR-X syndrome, also known as alpha-thalassemia mental retardation syndrome, is an X-linked recessive condition caused by a mutation in the ATRX gene on the X chromosome. Affected males typically show moderate intellectual disability together with distinctive physical characteristics, including coarse facial features, microcephaly, hypertelorism, a depressed nasal bridge, a tented upper lip and an everted lower lip. The condition also involves mild or moderate anemia associated with alpha-thalassemia, linking the neurological and blood-related features to the same underlying gene defect. Female carriers of the mutated gene generally show no specific signs, though some display skewed X chromosome inactivation, which can occasionally produce milder features in a small number of carriers.
Facts
Classification
ICD-10 ChapterIII: Diseases of the Blood and Blood-Forming Organs and Certain Disorders Involving the Immune Mechanism 1 Communicable or Non-communicable Causative Agent
Causative Agent (category) Sources
1. EMBL-EBI Ontology Lookup Service: alpha thalassemia-X-linked intellectual disability syndrome (DOID term)
EMBL-EBI Ontology Lookup Servicedatabase_cross_reference of the DOID term alpha thalassemia-X-linked intellectual disability syndrome; ICD-10 chapter derived from code D56.0 (WHO range D50-D89)Quote, database_cross_reference of the DOID term alpha thalassemia-X-linked intellectual disability syndrome; ICD-10 chapter derived from code D56.0 (WHO range D50-D89)
ICD10CM:D56.0
View the Source 2. ATR-X syndrome (Wikipedia)
Lead: disease category
Alpha-thalassemia mental retardation syndrome (ATRX), also called alpha-thalassemia X-linked intellectual disability syndrome, nondeletion type or ATR-X syndrome, is an X-linked recessive condition associated with a mutation in the ATRX gene.
Lead: causative agent category
Alpha-thalassemia mental retardation syndrome (ATRX), also called alpha-thalassemia X-linked intellectual disability syndrome, nondeletion type or ATR-X syndrome, is an X-linked recessive condition associated with a mutation in the ATRX gene.
View the SourceReader Challenges (0)
No disputes yet. Spotted an error or a better source? Open the first one.
Sign in to dispute this or suggest a correction.