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H Syndrome: A Case Report and Review of Literature
H syndrome is a rare autosomal recessive syndrome characterised by constellation of clinical features and systemic manifestations including cutaneous hyperpigmentation, hypertrichosis, hepatosplenomegaly, hearing loss, heart anomalies, hypogonadism, hyperglycaemia, low height, and hallux valgus. We...
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| Publicado no: | Indian J Dermatol |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications & Media Pvt Ltd
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5838761/ https://ncbi.nlm.nih.gov/pubmed/29527032 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/ijd.IJD_264_17 |
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