Global Variome shared LOVD
SLC38A8 (solute carrier family 38, member 8)
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Curator:
Mohammed A.M Derar
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Phenotype #0000331969
Individual ID
00442622
Associated disease
BTHLM
Diagnosis/Initial
Bethlem myopathy
Diagnosis/Definite
BTHLM1
Phenotype details
CK 800 IU/L; MRI muscle typical; muscle biopsy dystrophy; onset childhood; weakness cervical, proximal UL and LL; contractures elbows, ankles; no scoliosis; no cutaneous alterations; reduced maximal expiratory pressure
Inheritance
Unknown
Age/Examination
-
Age/Diagnosis
27y
Age/Onset
-
Phenotype/Onset
weakness
Protein
-
Owner name
Johan den Dunnen
Database submission
license
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International
Created by
Johan den Dunnen
Date created
2023-11-23 09:55:12 +01:00 (CET)
Date last edited
N/A
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