This item still needs to be validated !
ITEM METADATA RECORD
Title: Thrombocytopenia: first symptom in a patient with dyskeratosis congenita
Authors: De Boeck, Christiane ×
Degreef, Hugo
Verwilghen, Robrecht
Corbeel, Lucien
Casteels-Van Daele, M #
Issue Date: Jun-1981
Series Title: Pediatrics vol:67 issue:6 pages:898-903
Abstract: A case of dyskeratosis congenita is reported. This rare hereditary disease usually has the following progression: ectodermal dystrophy (reticular skin pigmentation, nail dystrophy, leukokeratosis of mucosal membranes), appearing in the first decade, followed in about 50% of these patients by a hematopoietic disorder resembling Fanconi's anemia, usually developing in the second or third decade. Carcinomas may occur in leukokeratotic areas in the third, fourth, or fifth decade. This patient's clinical course is interesting because the thrombocytopenia developed as an isolated symptom at the age of 5 years and preceded the skin anomalies by three years. The diagnosis of dyskeratosis congenita was made only after an evolution of five years. The diagnosis of dyskeratosis congenita--although it is a rare disease--should be considered in every child first seen with aplastic anemia or thrombocytopenia.
ISSN: 0031-4005
Publication status: published
KU Leuven publication type: IT
Appears in Collections:Laboratory of Dermatology
Pediatric Pulmonology Section (-)
× corresponding author
# (joint) last author

Files in This Item:

There are no files associated with this item.

Request a copy

 




All items in Lirias are protected by copyright, with all rights reserved.