Tags

Type your tag names separated by a space and hit enter

[The Zinsser-Cole-Engman syndrome. A contribution to congenital poikilodermias as well as a contribution to familial pancytopenias].
Z Hautkr. 1979 Apr 01; 54(7):273-86.ZH

Abstract

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.

Authors

Rodermund OE
No affiliation info available
Hausmann D
No affiliation info available
Hausmann G
No affiliation info available

MeSH

Anemia, AplasticDiagnosis, DifferentialHumansKeratosisLeukoplakia, OralPancytopeniaPigmentation DisordersRothmund-Thomson SyndromeSyndrome

Pub Type(s)

English Abstract
Journal Article
Review

Language

ger

PubMed ID

375602

Citation

Rodermund, O E., et al. "[The Zinsser-Cole-Engman Syndrome. a Contribution to Congenital Poikilodermias as Well as a Contribution to Familial Pancytopenias]." Zeitschrift Fur Hautkrankheiten, vol. 54, no. 7, 1979, pp. 273-86.
Rodermund OE, Hausmann D, Hausmann G. [The Zinsser-Cole-Engman syndrome. A contribution to congenital poikilodermias as well as a contribution to familial pancytopenias]. Z Hautkr. 1979;54(7):273-86.
Rodermund, O. E., Hausmann, D., & Hausmann, G. (1979). [The Zinsser-Cole-Engman syndrome. A contribution to congenital poikilodermias as well as a contribution to familial pancytopenias]. Zeitschrift Fur Hautkrankheiten, 54(7), 273-86.
Rodermund OE, Hausmann D, Hausmann G. [The Zinsser-Cole-Engman Syndrome. a Contribution to Congenital Poikilodermias as Well as a Contribution to Familial Pancytopenias]. Z Hautkr. 1979 Apr 1;54(7):273-86. PubMed PMID: 375602.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - [The Zinsser-Cole-Engman syndrome. A contribution to congenital poikilodermias as well as a contribution to familial pancytopenias]. AU - Rodermund,O E, AU - Hausmann,D, AU - Hausmann,G, PY - 1979/4/1/pubmed PY - 1979/4/1/medline PY - 1979/4/1/entrez SP - 273 EP - 86 JF - Zeitschrift fur Hautkrankheiten JO - Z Hautkr VL - 54 IS - 7 N2 - 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. SN - 0301-0481 UR - https://wwww.unboundmedicine.com/medline/citation/375602/[The_Zinsser_Cole_Engman_syndrome__A_contribution_to_congenital_poikilodermias_as_well_as_a_contribution_to_familial_pancytopenias]_ L2 - https://medlineplus.gov/skinpigmentationdisorders.html DB - PRIME DP - Unbound Medicine ER -