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Mseleni joint disease (MJD) is a rare and crippling chondrodysplasia, reported mainly in the Maputaland region in northern Kwazulu Natal, South Africa, characterized by a bilateral and uniform arthropathy of the joints that primarily and most severely affects the hip but that can also affect many other joints (i.e. knees, ankles, wrists, shoulders, elbows), and that manifests with pain and stiffness that progressively limits joint movement, eventually compromising a patient's ability to walk. Severe short staure and brachydactyly have been reported in a few patients with MJD.
Features include: Severe short stature.
Organ System | Phenotype Count | Example Features |
|---|---|---|
Growth and development | 1 | Severe short stature |
Estimated prevalence: Unknown (Unknown prevalence).
No clinical trials have been registered for brachydactylous dwarfism, Mseleni type.
1 publication has been identified in PubMed for brachydactylous dwarfism, Mseleni type. Research spans Epidemiology / Natural History (100%).
Dinkele ES (2026). [PMID: 42240353](https://pubmed.ncbi.nlm.nih.gov/42240353/). *Afr J Prim Health Care Fam Med*. [Epidemiology / Natural History]
Data assembled from 5 of 12 sources · Last updated Sep 20, 2026, 3:05 PM UTC
Online Mendelian Inheritance in Man
European rare disease database
Genetic and Rare Diseases Info Center