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urban-Rogers-Meyer syndrome - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

urban-Rogers-Meyer syndrome

MONDO:0009905

Also known as:Prader-Willi habitus-osteopenia-camptodactyly syndromeintellectual disability-short stature-hand contractures-genital anomalies syndromePrader-Willi habitus, osteopenia, and camptodactyly

Overview

This syndrome is characterized by intellectual deficit, short stature, obesity, genital abnormalities, and hand and/or toe contractures. It has been described in two brothers and in one isolated case. The patients also present with generalized osteoporosis and a history of frequent fractures. This syndrome is similar to Prader-Willi syndrome, but the hand contractures and osteoporosis, together with the lack of hypotonia, indicate this is a different entity.

Diagnosis

Biomarker and diagnostic research for urban-Rogers-Meyer syndrome has been reported in the published literature.

Prognosis

Estimated prevalence: <1 in 1,000,000 (VERY_RARE).

Research Landscape

Sourced from ClinicalTrials.gov and PubMed. Publication types are classified using NLM-curated article metadata; research type breakdowns reflect the nature of published work for this disease.

No clinical trials have been registered for urban-Rogers-Meyer syndrome.

100 publications have been identified in PubMed for urban-Rogers-Meyer syndrome. Research spans Review / Meta-Analysis (38%), Basic Science / Preclinical (27%), and Epidemiology / Natural History (9%).

Research Type	Count	% of Total
Research summaries	36	38%

Data assembled from 4 of 12 sources · Last updated Sep 19, 2026, 11:55 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:264010

Orphanet

European rare disease database

Orphanet:3409

GARD

Genetic and Rare Diseases Info Center

GARD:5426

Questions for Your Care Team

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urban-Rogers-Meyer syndrome

Overview

Diagnosis

Prognosis

Research Landscape

Medical References

External Resources

OMIM

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

Recent Publications