H syndrome: A rare genodermatosis

J Cosmet Dermatol. 2020 Sep;19(9):2449-2450. doi: 10.1111/jocd.13572. Epub 2020 Jul 12.

Authors

Isa An¹, Murat Ozturk², Erhan Ayhan³, Ibrahim Ibiloglu⁴

Affiliations

¹ Department of Dermatology, Sanlıurfa Training and Research Hospital, Sanlıurfa, Turkey.
² Department of Dermatology, Van Training and Research Hospital, Van, Turkey.
³ Department of Dermatology, University of Health Sciences Gazi Yaşargil Training and Research Hospital, Diyarbakır, Turkey.
⁴ Department of Pathology, Dicle University Medical Faculty, Diyarbakır, Turkey.

PMID: 32585061
DOI: 10.1111/jocd.13572

No abstract available

Publication types

Case Reports
Letter

MeSH terms

Child
Humans
Hyperpigmentation / genetics
Hyperpigmentation / pathology*
Hypertrichosis / genetics
Hypertrichosis / pathology*
Male
Nucleoside Transport Proteins / genetics
Point Mutation
Rare Diseases
Syndrome
Thigh / pathology

Substances

Nucleoside Transport Proteins
SLC29A3 protein, human