Open AccessH Syndrome: A case report and review of literature
Author(s) -
Durga Shankar Meena,
Payal Chauhan,
Neirita Hazarika,
Naveen Kumar Kansal
Publication year - 2018
Publication title -
indian journal of dermatology/indian journal of dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.395
H-Index - 36
eISSN - 1998-3611
pISSN - 0019-5154
DOI - 10.4103/ijd.ijd_264_17
Subject(s) - medicine , hypertrichosis , hepatosplenomegaly , dermatology , hyperpigmentation , valgus , pediatrics , pathology , surgery , disease
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.