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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...

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Bibliografiska uppgifter
I publikationen:Indian J Dermatol
Huvudupphovsmän: Meena, Dilip, Chauhan, Payal, Hazarika, Neirita, Kansal, Naveen Kumar
Materialtyp: Artigo
Språk:Inglês
Publicerad: Medknow Publications & Media Pvt Ltd 2018
Ämnen:
Länkar: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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