Phenotype #0000326787

Individual ID 00436664
Associated disease LGMDR3;LGMD2D
Phenotype details CK level 16408.3U/L; proximal muscle atrophy, beginning in lower extremities, weakness muscles shoulder/arms, difficulties climbing stairs/standing up/sitting; no lumbar lordosis
Diagnosis/Initial limb-girdle muscular dystrophy
Inheritance Familial, autosomal recessive
Diagnosis/Definite LGMDR3
Age/Examination 09y (9 years)
Age/Diagnosis 08y
Age/Onset 08y
Phenotype/Onset -
Protein -
Owner name Nguyen Hoang
Database submission license No license selected
Created by Nguyen Hoang
Date created 2023-09-27 04:39:30 +02:00 (CEST)
Date last edited 2025-11-04 17:05:02 +01:00 (CET)

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