Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia

MONDO:0008842

A rare autosomal recessive cerebellar ataxia (ARCA), characterized by progressive cerebellar ataxia associated with oculomotor apraxia, severe neuropathy, and hypoalbuminemia.

Also known as: AOA1, APTX oculomotor apraxia or related oculomotor disease, ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia, oculomotor apraxia or related oculomotor disease caused by mutation in APTX, EAOH, EOCA-HA, ataxia, adult-onset, with oculomotor apraxia, ataxia-oculomotor apraxia 1

3 clinical trials for this condition and its sub-types, 0 tagged with Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia itself.

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↑ DNA repair disease (105) ↑ Ataxia-telangiectasia-like disorder (1)

Including sub-types (3) Tagged with Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia (0)

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