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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Detalhes bibliográficos
Publicado no:Appl Clin Genet
Main Authors: Zaimi, Yosra, Ayari, Myriam, Mensi, Asma, Bel Hadj Kacem, Linda, Achouri, Leila, Bouzrara, Meriem, Said, Yosra, Mouelhi, Leila, Debbeche, Radhouane
Formato: Artigo
Idioma:Inglês
Publicado em: Dove 2021
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8055247/
https://ncbi.nlm.nih.gov/pubmed/33883924
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/TACG.S306298
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