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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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Detalles Bibliográficos
Autores principales:	Meena, Dilip, Chauhan, Payal, Hazarika, Neirita, Kansal, Naveen Kumar
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Medknow Publications & Media Pvt Ltd 2018
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5838761/ https://www.ncbi.nlm.nih.gov/pubmed/29527032 http://dx.doi.org/10.4103/ijd.IJD_264_17

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