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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Main Authors: Dilip Meena (Author), Payal Chauhan (Author), Neirita Hazarika (Author), Naveen Kumar Kansal (Author)
Formato: Libro
Publicado: Wolters Kluwer Medknow Publications, 2018-01-01T00:00:00Z.
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