Phenotype #0000156972

Individual ID 00208236
Associated disease migraine
Diagnosis/Initial familial hemiplegic migraine; Progressive Cerebellar Ataxia; Recurrent Coma
Diagnosis/Definite -
Phenotype details 1st HMA no language disturbances, 1st HMA no sensory disturbances, 1st HMA no visual disturbances, 1st HMA no confusion/somnolence; 1st severe attack signs mild coma/fever; PermCer status, no nystagmus, dysarthria, no ataxia, CT scan cerebellar atrophy
Inheritance Familial
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Owner name LOVD
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2008-06-18 23:00:08 +02:00 (CEST)
Date last edited 2008-06-18 23:00:08 +02:00 (CEST)

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