Phenotype #0000284030

Individual ID 00390493
Associated disease MDDG
Phenotype details limb-girdle muscular dystrophy; 1y-walk, difficulty run and jump; no contractures; no intellectual disability; seizures; CK level 1200-7212 IU/L; EMG myogenic; ECG-normal; UCG-normal
Diagnosis/Initial muscle-eye-brain disease
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination 8y3m (8 years, 3 months)
Age/Diagnosis -
Age/Onset 1y9m
Phenotype/Onset muscle weakness after infection
Protein -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2021-11-10 16:44:31 +01:00 (CET)
Date last edited N/A

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