Disease #05760 (EA (ataxia, episodic (EA)))

Official abbreviation EA
Name ataxia, episodic (EA)
OMIM ID -
Inheritance -
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 0 genes -
Associated tissues -
Disease features -
Remarks -
Date created 2020-06-05 18:59:48 +02:00 (CEST)
Date last edited N/A


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00303088 Fam3 PubMed: Waters 2019 3-generation family, affected father/daugther F - Canada - - - - - EA 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 - CACNA1A, HSD17B10 2 2 Johan den Dunnen
00372758 179030 - - F ? Germany - - - - - EA For decades, secondary seizures with visual disturbance, gait disturbance, tendency to fall and sensory disturbances, cramps SCN2A SCN2A 1 1 Andreas Laner
00377136 181230 - - M no Germany - - - - - EA Ataxia, Episodic ataxia, Abnormality of coordination SCN2A SCN2A 1 1 Andreas Laner
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