autosomal recessive limb-girdle muscular dystrophy type 2F
MeSH: C535896ORPHA: 219
Overview
autosomal recessive limb-girdle muscular dystrophy that has material basis in mutation in the sarcoglycan-delta gene (SGCD)
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with autosomal recessive limb-girdle muscular dystrophy type 2F, sourced from HPO and Orphanet clinical annotations.
Shuffling gaitScapular wingingProximal upper limb amyotrophyProximal lower limb amyotrophyGeneralized limb muscle atrophyFacial palsy
Classification & Codes
MeSH Code
C535896Orphanet Code
ORPHA:219autosomal recessive limb-girdle muscular dystrophy type 2F
| MeSH | C535896 |
| Orphanet | ORPHA:219 |
| Treatments | 0 drug(s) |
| Symptoms on record | 6 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO