Disease #05656 (LGMDD4;LGMD1I (dystrophy, muscular, limb-girdle, autosomal dominant, type 4 (LGMDD-4, LGMD-1I)), OMIM:618129)

Official abbreviation LGMDD4;LGMD1I
Name dystrophy, muscular, limb-girdle, autosomal dominant, type 4 (LGMDD-4, LGMD-1I)
OMIM ID 618129
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 3
Phenotype entries for this disease 2
Associated with 1 gene CAPN3
Associated tissues -
Disease features -
Remarks autosomal dominant
Date created 2019-09-16 23:11:06 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00335325 - - - M no (United States) White - - - - LGMDD4;LGMD1I - COL6A2 COL6A2 1 1 Melissa Fries
00448143 Pat4 PubMed: Krag 2025 2-generation family, 1 affected, unaffected parents M no Reunion - - - - - LGMDD4;LGMD1I see paper; ..., 57y-myalgia thighs, elevated circulating creatine kinase concentration (HP:0003236) 2000 U/L; 60y-waddling gait, CK level 5000 U/L; myopathy (HP:0003198), centrally nucleated skeletal muscle fibers (HP:0003687), proximal muscle weakness (HP:0003701) CAPN3 CAPN3 1 1 Camille Verebi
00448369 FamPatII1 PubMed: Mao 2024 2-generation family, affected mother/son/daughter M - China - - - - - LGMDD4;LGMD1I see paper; ..., 8y-slow, progressive weakness muscles, abnormal gait; 10y-slow, progressive weakness lower limbs, frequent falls, difficulty in standing, walking and climbing stairs; 16y-only walk unaided for <15 min, unable to raise arms above head, no sensory/ocular/bulbar abnormalities, severe weakness proximal muscles all limbs, pelvic and shoulder girdles; 16y-normal mental status, no oculomotor/facial abnormalities with sensory and coordination examinations also finding no abnormalities CAPN3 CAPN3 1 4 Johan den Dunnen
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