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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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| Publicat a: | Appl Clin Genet |
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| Autors principals: | , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Dove
2021
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| Matèries: | |
| Accés en línia: | 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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