Dyschromatosis universalis hereditaria View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2003-04

AUTHORS

I. Elser, A. S. Hassan, J. Rieker, T. Ruzicka, M. Megahed

ABSTRACT

A 30-year old male patient presented with a rare congenital pigment disturbance, dyschromatosis universalis hereditaria. Clinically, he displayed mottled hyperpigmentation covering almost the entire skin surface with accentuation in skin folds. The lesions had been present since birth. He was the only family member showing these changes. He had no other medical problems and took no medications. More... »

PAGES

368-370

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s00105-003-0505-6

DOI

http://dx.doi.org/10.1007/s00105-003-0505-6

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1037320041

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/12669214


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