Phenotypes for disease #05760 (EA (ataxia, episodic (EA)))

3 entries on 1 page. Showing entries 1 - 3.
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0000230172 episodic ataxia EA2 8w-developmental delay, possible vision problems, signs of mild intellectual deficiency in both parents; 4m-developmental delay, mild axial hypotonia, suspected cortical blindness, no persistent vision problems; walk-15m, speechfew words; MRI brain 23m-normal Familial, autosomal dominant - - 00y00m56d - Johan den Dunnen 00303088
0000268035 - - For decades, secondary seizures with visual disturbance, gait disturbance, tendency to fall and sensory disturbances, cramps Unknown 65y - - - Andreas Laner 00372758
0000272299 - - Ataxia, Episodic ataxia, Abnormality of coordination Unknown - 02y - - Andreas Laner 00377136
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