The histopathology and phenotypic variability in H syndrome-Reference-Cited by-同舟云学术

The histopathology and phenotypic variability in H syndrome

Published:2018-01-25 Issue:3 Volume:6 Page:476-478
ISSN:2050-0904
Container-title:Clinical Case Reports
language:en
Short-container-title:Clin Case Rep

Author:

Dias-Polak David¹^ORCID,Indelman Margarita²,Bergman Reuven¹²,Avitan-Hersh Emily¹²

Affiliation:

1. Department of Dermatology; Rambam Health Care Campus; HaAliya HaShniya St 8, Haifa POB 9602 Haifa 31096 Israel

2. Laboratory of Molecular Dermatology; The Bruce Rappaport Faculty of Medicine, Technion; Rambam Health Care Campus; HaAliya HaShniya St 8, Haifa POB 9602 Haifa 31096 Israel

Publisher

Wiley

Subject

General Medicine

Reference12 articles.

1. The H syndrome is caused by mutations in the nucleoside transporter hENT3;Molho-Pessach;Am. J. Hum. Genet.,2008

2. The H syndrome: two novel mutations affecting the same amino acid residue of hENT3;Molho-Pessach;J. Dermatol. Sci.,2010

3. H syndrome: novel and recurrent mutations in SLC29A3;Priya;Br. J. Dermatol.,2010

4. A case of H syndrome showing immunophenotype similarities to Rosai-Dorfman disease;Avitan-Hersh;Am. J. Dermatopathol.,2011

5. Emperipolesis: an additional common histopathologic finding in H syndrome and Rosai-Dorfman disease;Colmenero;Am. J. Dermatopathol.,2012

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3. Mycophenolate mofetil treatment of an H syndrome patient with a SLC29A3 mutation;Dermatologic Therapy;2020-10-26