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Mesomelic dwarfism, Reinhardt-Pfeiffer type is characterized by disproportionate short stature from birth with dysplasia of the ulna and fibula.
Biomarker and diagnostic research for mesomelic dwarfism, Reinhardt-Pfeiffer type has been reported in the published literature.
Estimated prevalence: Unknown (Unknown prevalence).
No clinical trials have been registered for mesomelic dwarfism, Reinhardt-Pfeiffer type.
5 publications have been identified in PubMed for mesomelic dwarfism, Reinhardt-Pfeiffer type. Research spans Case Report / Case Series (40%), Other (20%), and Diagnostic / Biomarker (20%).
Manasra MR (2025). [PMID: 40046165](https://pubmed.ncbi.nlm.nih.gov/40046165/). *BJR case reports*. [Case Report / Case Series]
Obstetrics And Gynecology Ultrasound Group Ultrasound Branch Of Chinese Medical Association L (2025). [PMID: 40947403](https://pubmed.ncbi.nlm.nih.gov/40947403/). *Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics*. [Other]
Katchburian M (2024). [PMID: 38924895](https://pubmed.ncbi.nlm.nih.gov/38924895/). *Journal of plastic, reconstructive & aesthetic surgery : JPRAS*. [Case Report / Case Series]
Lee HYD (2024). [PMID: 39054063](https://pubmed.ncbi.nlm.nih.gov/39054063/). *The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians*. [Epidemiology / Natural History]
Data assembled from 4 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
Wall LB (2024). [PMID: 38916216](https://pubmed.ncbi.nlm.nih.gov/38916216/). *Journal of pediatric orthopedics*. [Diagnostic / Biomarker]