H Syndrome: A Case Report and Review of Literature
Dilip Meena1, Payal Chauhan1, Neirita Hazarika1
1Department of Dermatology, Venereology and Leprology, All India Institute of Medical Sciences, Rishikesh, Uttarakhand, India.
Abstract:
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 report a case of this syndrome with typical clinical findings. We report this case citing the rarity of this uncommon entity.
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