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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease choreoacanthocytosis
Comorbidity C0000744|acanthocytosis
Sentences 2
PubMedID- 24529944 This rare syndrome together with autosomal recessive chorea-acanthocytosis forms the core of the neuroacanthocytosis syndromes, both featuring an estimated prevalence of less than 1–5/1,000,000 [2].
PubMedID- 19497603 Introduction: chorea-acanthocytosis (chac) is one of the neuroacanthocytosis syndromes which form a group of disorders characterized by the association of neurological abnormalities and spiculated red blood cells called acanthocytes.

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