Beukes familial hip dysplasia: An autosomal dominant entity
- 1 August 1990
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 36 (4) , 386-390
- https://doi.org/10.1002/ajmg.1320360403
Abstract
An unique inherited skeletal disorder had been identified in 47 patients in 6 generations of an Afrikaner family in Southern Africa. Pain develops in the hip joints in early childhood in the majority of affected persons and the course is progressive with severe crippling by early adulthood. General health is good, height is not significantly reduced, and there is no extra-skeletal involvement. The major changes are in the femoral capital epiphyses, which are severely flattened and irregular; secondary osteoarthrosis develops at an early age. Pedigree data indicate autosomal dominant inheritance with a reasonably consistent phenotypic expression. In view of the fact that only members of the Beukes family have been identified as suffering from the condition, the designation “Beukes familial hip dysplasia” (BFHD) is proposed.Keywords
This publication has 5 references indexed in Scilit:
- Namaqualand Hip Dysplasia Orthopedic ImplicationsPublished by Wolters Kluwer Health ,1987
- Namaqualand hip dysplasia: An autosomal dominant entityAmerican Journal of Medical Genetics, 1984
- Primary Osteoarthritis of the Hip:Interrelationship between Intraosseous Pressure, X-ray Changes, Clinical Severity and Bone DensityActa Orthopaedica, 1981
- Dysplasia Epiphysealis Capitis Femoris: A Clinical-radiological Syndrome and its Relationship to Legg-Calvé-Perthes DiseaseActa Orthopaedica, 1964
- Hereditary Legg-Calvé-Perthes DiseaseArchives of Pediatrics & Adolescent Medicine, 1963