Phenotype #0000139643

Individual ID 00174816
Associated disease LGMD
Phenotype details onset overt symptoms childhood; CPK raised 33x; limb-girdle weakness, waddling gait; improvement after corticosteroid treatment; Mi2-antibodies
Diagnosis/Initial proximal myopathy
Inheritance Isolated (sporadic)
Diagnosis/Definite -
Age/Examination 06y (6 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
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 2018-08-10 19:10:48 +02:00 (CEST)
Date last edited 2020-02-10 15:53:14 +01:00 (CET)

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