The Zinsser-Cole-Engman syndrome. a contribution to congenital poikilodermias as well as a contribution to familial pancytopenias
Rodermund, O.E.; Hausmann, D.; Hausmann, G.
Zeitschrift für Hautkrankheiten 54(7): 273-286
1979
ISSN/ISBN: 0301-0481 PMID: 375602 Document Number: 141750
The Zinser-Cole-Engman-syndrome (Dyskeratosis congenita), which is characterized by the cardinal symptoms pigmentatio reticularis, onychodystrophia and leukoplakia oris, is discussed as a clinical entity, which is different from Fanconi's anemia and Braun-Falco-Marghescu-syndrome. A review of the literature is given.
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