Dyskeratosis congenita: An autosomal recessive variant
- 4 March 1999
- journal article
- case report
- Published by Wiley in American Journal of Medical Genetics
- Vol. 83 (3) , 178-182
Abstract
We describe a woman with dyskeratosis congenita (DKC), microcephaly, and a purple discoloration of the tongue. The latter findings are not commonly described in males with DKC, have been reported in another female patient with this condition, and may represent the phenotype of an autosomal recessive entity of DKC. Results of X chromosome inactivation studies did not support X‐linked DKC in our family. The additional findings of an affected brother and parental consanguinity support the hypothesis of autosomal recessive inheritance. Am. J. Med. Genet. 83:178–182, 1999.Keywords
This publication has 11 references indexed in Scilit:
- X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functionsNature Genetics, 1998
- Dyskeratosis congenita: an inherited bone marrow failure syndromeBritish Journal of Haematology, 1996
- Dyskeratosis CongenitaDermatologic Clinics, 1995
- Dyskeratosis Congenita with Esophageal Stricture and Dermatological ManifestationsEndoscopy, 1994
- Gastrointestinal involvement in a woman with dyskeratosis congenitaDigestive Diseases and Sciences, 1993
- Etiologic heterogeneity in dyskeratosis congenitaAmerican Journal of Medical Genetics, 1989
- Dyskeratosis congenita.Journal of Medical Genetics, 1988
- Dyskeratosis Congenita in a Girl Simulating Chronic Graft-vs-Host DiseaseArchives of Dermatology, 1985
- DYSKERATOSIS CONGENITAAustralasian Journal of Dermatology, 1965
- Dyskeratosis CongenitaArchives of Dermatology, 1963