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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...
Gorde:
| Argitaratua izan da: | Indian J Dermatol |
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| Egile Nagusiak: | , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Medknow Publications & Media Pvt Ltd
2018
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| Gaiak: | |
| Sarrera elektronikoa: | 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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