H Syndrome - A Case Report

This case report describes a case of H syndrome with characteristic cutaneous hyperpigmentation, hypertrichosis, sclerodermatous thickening, and multisystem involvement such as hearing loss and heart anomaly in an Indian patient. There are around 100 cases of this rare, autosomal recessive genoderma...

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Detalles Bibliográficos
Autores principales: Yesudian, Patrick, Sarveswari, K. N., Karrunya, K. J., Thomas, Kuruvilla
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6536078/
https://www.ncbi.nlm.nih.gov/pubmed/31149577
http://dx.doi.org/10.4103/idoj.IDOJ_187_18

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6536078/
https://www.ncbi.nlm.nih.gov/pubmed/31149577
http://dx.doi.org/10.4103/idoj.IDOJ_187_18

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