Congenital Dyskeratosis
- 1 November 1972
- journal article
- research article
- Published by American Medical Association (AMA) in American Journal of Diseases of Children
- Vol. 124 (5) , 701-704
- https://doi.org/10.1001/archpedi.1972.02110170079012
Abstract
A child with the typical features of congenital dyskeratosis (Zinsser-Engman-Cole syndrome) and aplastic anemia, low serum γ-globulins, thymic dysplasia, lymphocyte-poor spleen and lymph nodes, and absence of primary follicles, is reported. The findings support an immunological defect and suggest that thymic dysplasia may be an integral feature of congenital dyskeratosis.Keywords
This publication has 3 references indexed in Scilit:
- Familial Pancytopenia with Congenital Abnormalities (Fanconi Syndrome)Acta Medica Scandinavica, 2009
- Zur Kenntnis der Poikilodermie, Parapsoriasis und Atrophia cutis reticularis cum pigmentatione, dystrophia unguium et leukoplakia oris Zinsser-?Dyskeratois congenita?Archives of Dermatological Research, 1956
- CONGENITAL ATROPHY OF THE SKIN, WITH RETICULAR PIGMENTATIONJAMA, 1935