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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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Indian J Dermatol
Egile Nagusiak: Meena, Dilip, Chauhan, Payal, Hazarika, Neirita, Kansal, Naveen Kumar
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Medknow Publications & Media Pvt Ltd 2018
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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