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PedAM

Pediatric Disease Annotations & Medicines




Disease thalassemia
Phenotype C0025362|mental retardation
Sentences 5
PubMedID- 20507641 Also patients with a rare form of syndromal x-linked mental retardation associated with α thalassaemia have been described, in which the intellectual disability is more severe and the dysmorphic features show striking similarities among patients.
PubMedID- 26026117 We studied telomere length abnormalities, telomerase rna component (terc) expression, alpha-thalassemia x-linked mental retardation (atrx) expression, and death domain-associated protein (daxx) expression in gastroenteropancreatic neuroendocrine tumors (gep-nets).
PubMedID- 25976463 Alpha-thalassemia x-linked mental retardation syndrome is a rare inherited intellectual disability disorder due to mutations in the atrx gene.
PubMedID- 21505078 Atrx is a member of the snf2 family of chromatin-remodelling proteins and is mutated in an x-linked mental retardation syndrome associated with alpha-thalassaemia (atr-x syndrome).
PubMedID- 22089611 Atr-x syndrome, formally called alpha-thalassaemia x-linked mental retardation syndrome results from an abnormality in the atrx gene.

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