Phenotype #0000159195

Individual ID 00210630
Associated disease CGL
Diagnosis/Initial congenital lipodystrophy, muscular dystrophy
Diagnosis/Definite CGL-4
Phenotype details no acanthosis nigricans, hepatosplenomegaly, reduced growth hormone secretion, distal dominant muscle weakness, muscle mounding, muscle hypertrophy, caridac arrhythmia, lordosis, contractures (ankles, shoulders, fingers), constipation; CPK 1374; no intellectual disability
Inheritance Unknown
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
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 2009-11-07 16:58:46 +01:00 (CET)
Date last edited 2013-02-01 19:44:12 +01:00 (CET)

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