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Article

H syndrome: a multifaceted histiocytic disorder with hyperpigmentation and hypertrichosis.

Acta dermato-venereologica - 1 Nov 2015

Tekin Burak, Atay Zeynep, Ergun Tulin, Can Meryem, Tuney Davut, Babay Sofia, Turan Serap, Bereket Abdullah, Zlotogorski Abraham, Molho-Pessach Vered

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Share to Child
Share to Hearing Loss, Sensorineural
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 26015165
DOI: 10.2340/00015555-2145

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Related research

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H syndrome: a multifaceted histiocytic disorder with hyperpigmentation and hypertrichosis.PMID 26015165Read ↗

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H syndrome: A review of treatment options and a hypothesis of phenotypic variability.Semantic proximity Read ↗

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H syndrome: the first 79 patients.Semantic proximity Read ↗

[H syndrome: First reported paediatric case in Latin America].Semantic proximity Read ↗

'H-syndrome': a multisystem genetic disorder with cutaneous clues.Semantic proximity Read ↗

Mutations in SLC29A3, encoding an equilibrative nucleoside transporter ENT3, cause a familial histiocytosis syndrome (Faisalabad histiocytosis) and familial Rosai-Dorfman disease.Semantic proximity Read ↗

An Egyptian family with H syndrome due to a novel mutation in SLC29A3 illustrating overlapping features with pigmented hypertrichotic dermatosis with insulin-dependent diabetes and Faisalabad histiocytosis.Semantic proximity Read ↗

H syndrome: novel and recurrent mutations in SLC29A3.Semantic proximity Read ↗

Hereditary hypo/de-pigmented dermatoses: an overview.Semantic proximity Read ↗

GLMN variants cause skin hyperpigmentation: a promising potential therapeutic target.Semantic proximity Read ↗

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