[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.
MeSH
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 -