Sex‐linked chondrodysplasia punctata?
- 1 January 1977
- journal article
- research article
- Published by Wiley in Clinical Genetics
- Vol. 11 (1), 73-76
- https://doi.org/10.1111/j.1399-0004.1977.tb01281.x
Abstract
Widespread atrophic lesions and pigmentary disturbances of the skin, distributed in a linear or whorled pattern, are seen in some patients with chondrodysplasia punctata of the Conradi-Huenermann type. This association of anomalies constitutes a distinct genetic disorder, which is inherited as an X-linked dominant trait lethal in hemizygous males.This publication has 7 references indexed in Scilit:
- Heterogeneity of Chondrodysplasia punctataHuman Genetics, 1971
- Conradi's diseaseThe Journal of Pediatrics, 1968
- Skin Manifestations of Conradi's DiseaseArchives of Dermatology, 1966
- Skin manifestations of Conradi's disease. Chondrodystrophia congenita punctataArchives of Dermatology, 1966
- Chondrodystrophia Congenita Punctata (Conradi's Disease)American Journal of Diseases of Children, 1960
- Follicular Atrophoderma and Pseudopelade Associated with Chondrodystrophia Calcificans Congenita**From the Department of Dermatology, College of Physicians and Surgeons, Columbia University, and the Vanderbilt Clinic.Journal of Investigative Dermatology, 1949
- II. Demonstrationen – DémonstrationsDermatology, 1944