Phenotype #0000343687

Individual ID 00455095
Associated disease LGMD2
Phenotype details see paper; ..., myopathic pattern; 1st muscle weakness pelvic-femoral girdles; muscle weakness pelvic-femoral girdles, ll distal muscle; still ambulant; no contractures ; serum CK level 130 ukat/l
Diagnosis/Initial limb-girdle muscular dystrophy
Diagnosis/Definite LGMDR1
Inheritance Familial, autosomal recessive
Age/Examination 9y (9 years)
Age/Onset 7y
Phenotype/Onset -
Age/Diagnosis -
Protein normal IHC; WB CAPN3 no 94, 60, 30 kDa, labelling on 45 kDa
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 2024-10-01 20:00:32 +02:00 (CEST)
Date last edited N/A

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