Pseudo-Meigs’ Syndrome in Tunisian H Syndrome Female Patient: First Case Reported

H syndrome is an extremely rare autosomal recessive affection caused by biallelic mutations in the SLC29A3 gene encoding the human equilibrative nucleoside transporter hENT3. The hallmark signs are cutaneous consisting of hyperpigmentation and hypertrichosis patches. Besides, associated systemic man...

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Detalles Bibliográficos
Autores principales: Zaimi, Yosra, Ayari, Myriam, Mensi, Asma, Bel Hadj Kacem, Linda, Achouri, Leila, Bouzrara, Meriem, Said, Yosra, Mouelhi, Leila, Debbeche, Radhouane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8055247/
https://www.ncbi.nlm.nih.gov/pubmed/33883924
http://dx.doi.org/10.2147/TACG.S306298

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8055247/
https://www.ncbi.nlm.nih.gov/pubmed/33883924
http://dx.doi.org/10.2147/TACG.S306298

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