Phenotype #0000106138

Individual ID 00133391
Associated disease LGMDR5;LGMD2C
Phenotype details severe (clinical grade VII), walk tip-toe; 14y-inable to walk (HP:0002540)
Diagnosis/Initial severe autosomal recessive muscular dystrophy, North African type (SCARMD)
Inheritance Isolated (sporadic)
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis 6y
Age/Onset 6y
Phenotype/Onset difficulty climbing stairs/running
Protein IHC no SGCA, WB SGCA trace
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 2007-07-02 13:52:57 +02:00 (CEST)
Date last edited 2012-03-09 18:58:40 +01:00 (CET)

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