사지대근이영양증
사지대근이영양증은 유전 양상(그리고 진단의 충분성 역시 다양한)이 서로 다른 여러 하위 유형을 통칭하는 질환입니다. 이 질환과 관련된 변이를 보유하고 계신 경우, 확진을 위해 근골격계 전문의의 상담을 받으시기 바랍니다.
분석 유전자
다른 명칭
Leyden-Mobius muscular dystrophy; LGMD
관련 하위 유형 45개 포함 ↓하위 유형 숨기기 ↑
- autosomal dominant limb-girdle muscular dystrophy type 1D (DNAJB6)
- autosomal dominant limb-girdle muscular dystrophy type 1E (DES)
- autosomal dominant limb-girdle muscular dystrophy type 1F
- autosomal dominant limb-girdle muscular dystrophy type 1G
- autosomal dominant limb-girdle muscular dystrophy type 1H
- autosomal recessive limb-girdle muscular dystrophy
- autosomal recessive limb-girdle muscular dystrophy type 2A
- autosomal recessive limb-girdle muscular dystrophy type 2B
- autosomal recessive limb-girdle muscular dystrophy type 2C
- autosomal recessive limb-girdle muscular dystrophy type 2D
- autosomal recessive limb-girdle muscular dystrophy type 2E
- autosomal recessive limb-girdle muscular dystrophy type 2F
- autosomal recessive limb-girdle muscular dystrophy type 2G
- autosomal recessive limb-girdle muscular dystrophy type 2H
- autosomal recessive limb-girdle muscular dystrophy type 2I
- autosomal recessive limb-girdle muscular dystrophy type 2J
- autosomal recessive limb-girdle muscular dystrophy type 2K
- autosomal recessive limb-girdle muscular dystrophy type 2L
- autosomal recessive limb-girdle muscular dystrophy type 2M
- autosomal recessive limb-girdle muscular dystrophy type 2N
- autosomal recessive limb-girdle muscular dystrophy type 2O
- autosomal recessive limb-girdle muscular dystrophy type 2P
- autosomal recessive limb-girdle muscular dystrophy type 2Q
- autosomal recessive limb-girdle muscular dystrophy type 2R1
- autosomal recessive limb-girdle muscular dystrophy type 2T
- autosomal recessive limb-girdle muscular dystrophy type 2U
- autosomal recessive limb-girdle muscular dystrophy type 2W
- autosomal recessive limb-girdle muscular dystrophy type 2X
- autosomal recessive limb-girdle muscular dystrophy type 2Y
- autosomal recessive limb-girdle muscular dystrophy type R18
- Bethlem myopathy 1A
- Emery-Dreifuss muscular dystrophy 2, autosomal dominant
- epidermolysis bullosa simplex 5B, with muscular dystrophy
- limb-girdle muscular dystrophy due to POMK deficiency
- muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 8
- muscular dystrophy, limb-girdle, autosomal dominant
- muscular dystrophy, limb-girdle, autosomal dominant 4
- muscular dystrophy, limb-girdle, autosomal recessive 23
- muscular dystrophy, limb-girdle, autosomal recessive 26
- muscular dystrophy, limb-girdle, autosomal recessive 27
- muscular dystrophy, limb-girdle, autosomal recessive 28
- muscular dystrophy, limb-girdle, autosomal recessive 29
- myofibrillar myopathy 3
- POMGNT2-related limb-girdle muscular dystrophy R24
- Ullrich congenital muscular dystrophy 1A
