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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Detalles Bibliográficos
Autores principales: Saleh Anaraki, Kimia, Khosravi, Sepehr, Behrangi, Elham, Sadeghzadeh-Bazargan, Afsaneh, Goodarzi, Azadeh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9051674/
https://www.ncbi.nlm.nih.gov/pubmed/35495792
http://dx.doi.org/10.4103/jfmpc.jfmpc_1435_21

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9051674/
https://www.ncbi.nlm.nih.gov/pubmed/35495792
http://dx.doi.org/10.4103/jfmpc.jfmpc_1435_21

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