camptobrachydactyly https://rarediseases.info.nih.gov/diseases/1062/camptobrachydactyly https://www.malacards.org/card/camptobrachydactyly Camptobrachydactyly is an extremely rare brachydactyly syndrome, characterized by short broad hands and feet with brachydactyly associated with congenital flexion contractures of the proximal and/or distal interphalangeal joints of the fingers, as well as syndactyly of feet. Polydactyly, septate vagina and urinary incontinence were also occasionally reported. Camptobrachydactyly has been described in 18 members of 1 family, suggesting an autosomal dominant inheritance. There have been no further descriptions in the literature since 1972. short foot/brachydactyly of toes, camptodactyly, brachydactyly OMIM:114150 UMLS:C1861963 MESH:C537967 MEDGEN:349399 GARD:0001062 camptobrachydactyly Orphanet:1319 SCTID:733045005 MONDO:0007249 brachydactyly