Dyskeratosis congenita. Report of a large kindred
- 1 September 1981
- journal article
- research article
- Published by Oxford University Press (OUP) in British Journal of Dermatology
- Vol. 105 (3) , 321-325
- https://doi.org/10.1111/j.1365-2133.1981.tb01292.x
Abstract
This kindred includes six males with dyskeratosis congenita. It is the largest British pedigree so far reported and brings the total number of reported cases to fifty-nine. Our pedigree supports X-linked recessive inheritance and close linkage with the Xg2 locus was excluded. Three previously unreported complications are noted; Hodgkin's disease, adenocarcinoma of the pancreas and deafness. Normal chromosomal stability was found in three patients and immunological studies precluded an early universal defect in cell-mediated immunity.This publication has 4 references indexed in Scilit:
- X-linked dyskeratosis congenita with pancytopeniaArchives of Dermatology, 1978
- Dyskeratosis congenita: clinical features and genetic aspects. Report of a family and review of the literature.Journal of Medical Genetics, 1975
- Dyskeratosis Congenita With PancytopeniaAmerican Journal of Diseases of Children, 1973
- Congenital DyskeratosisAmerican Journal of Diseases of Children, 1972