H Syndrome: A case report and review of literature | Zendy

Neirita Hazarika | Zendy; Dilip Meena | Zendy; Payal Chauhan | Zendy; Naveen Kumar Kansal | Zendy

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H Syndrome: A case report and review of literature

Author(s) -

Neirita Hazarika,

Dilip Meena,

Payal Chauhan,

Naveen Kumar Kansal

Publication year - 2018

Publication title -

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.

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