H syndrome: Clinical, histological and genetic investigation in Tunisian patients-Reference-Cited by-同舟云学术

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H syndrome: Clinical, histological and genetic investigation in Tunisian patients

Published:2018-05-29 Issue:8 Volume:45 Page:978-985
ISSN:0385-2407
Container-title:The Journal of Dermatology
language:en
Short-container-title:J Dermatol

Author:

Jaouadi Hager¹^ORCID,Zaouak Anissa¹²,Sellami Khadija³,Messaoud Olfa¹,Chargui Mariem¹,Hammami Houda²,Jones Meriem⁴,Jouini Raja⁵,Chadli Debbiche Achraf⁵,Chraiet Karima⁶,Fenniche Sami²,Mrad Ridha⁷,Mokni Mourad⁸,Turki Hamida³,Benkhalifa Rym⁹,Abdelhak Sonia¹

Affiliation:

1. Biomedical Genomics and Oncogenetics Laboratory LR16IPT05; Pasteur Institute of Tunis; Tunis El Manar University; Tunis Tunisia

2. Department of Dermatology; Habib Thameur Hospital; Tunis Tunisia

3. Department of Dermatology; Hedi Chaker Hospital; Sfax Tunisia

4. Department of Dermatology; Charles Nicolle Hospital; Tunis Tunisia

5. Department of Pathology; Habib Thameur Hospital; Tunis Tunisia

6. Department of Pediatrics; Mohamed Tahar Maamouri Hospital; Nabeul Tunisia

7. Department of Congenital and Hereditary Diseases; Charles Nicolle Hospital; Tunis Tunisia

8. Department of Dermatology; La Rabta Hospital; Tunis Tunisia

9. Venoms and Therapeutic Biomolecules Laboratory LR16IPT08; Pasteur Institute of Tunis; Tunis Tunisia

Funder

Tunisian Ministry of Public Health

The Tunisian Ministry of Higher Education and Scientific Research

Publisher

Wiley

Subject

Dermatology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/1346-8138.14359/fullpdf

Reference32 articles.

1. The H syndrome: a genodermatosis characterized by indurated, hyperpigmented, and hypertrichotic skin with systemic manifestations;Molho-Pessach;J Am Acad Dermatol,2008

2. H syndrome: the first 79 patients;Molho-Pessach;J Am Acad Dermatol,2014

3. H syndrome: recently defined genodermatosis with distinct histologic features. A morphological, histochemical, immunohistochemical, and ultrastructural study of 10 cases;Doviner;Am J Dermatopathol,2010

4. Expanding the clinical spectrum of SLC29A3 gene defects;Spiegel;Eur J Med Genet,2010

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

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