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Mesomelic dysplasia Kantaputra type (MDK) is a rare skeletal disease characterized by symmetric shortening of the middle segments of limbs and short stature.
Features include: Mesomelia, Tarsal synostosis, Radial bowing, and Carpal synostosis.
Estimated prevalence: <1 in 1,000,000 (VERY_RARE).
No clinical trials have been registered for mesomelic dysplasia, Kantaputra type.
1 publication has been identified in PubMed for mesomelic dysplasia, Kantaputra type. Research spans Epidemiology / Natural History (100%).
Pagnamenta AT (2024). [PMID: 38776926](https://pubmed.ncbi.nlm.nih.gov/38776926/). *American journal of human genetics*. [Epidemiology / Natural History]
Data assembled from 5 of 12 sources · Last updated Sep 20, 2026, 11:13 AM UTC
Online Mendelian Inheritance in Man
European rare disease database
Genetic and Rare Diseases Info Center