Review of the current literature on H syndrome treatment

H syndrome is a systemic inherited autosomal recessive histiocytosis, with characteristic cutaneous findings accompanying systemic manifestations and a most common genetic mutation (OMIM 612391) as SLC29A3. The term “H Syndrome” is representative of presentation with hyperpigmentation, hypertrichosi...

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Bibliographic Details
Main Authors: Kimia Saleh Anaraki, Sepehr Khosravi, Elham Behrangi, Afsaneh Sadeghzadeh-Bazargan, Azadeh Goodarzi
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2022-01-01
Series:Journal of Family Medicine and Primary Care
Subjects:
Online Access:http://www.jfmpc.com/article.asp?issn=2249-4863;year=2022;volume=11;issue=3;spage=857;epage=860;aulast=Anaraki