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...

Descripción completa

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
_version_ 1783304299517837312
author Meena, Dilip
Chauhan, Payal
Hazarika, Neirita
Kansal, Naveen Kumar
author_facet Meena, Dilip
Chauhan, Payal
Hazarika, Neirita
Kansal, Naveen Kumar
author_sort Meena, Dilip
collection PubMed
description 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.
format Online
Article
Text
id pubmed-5838761
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Medknow Publications & Media Pvt Ltd
record_format MEDLINE/PubMed
spelling pubmed-58387612018-03-09 H Syndrome: A Case Report and Review of Literature Meena, Dilip Chauhan, Payal Hazarika, Neirita Kansal, Naveen Kumar Indian J Dermatol Case Report 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. Medknow Publications & Media Pvt Ltd 2018 /pmc/articles/PMC5838761/ /pubmed/29527032 http://dx.doi.org/10.4103/ijd.IJD_264_17 Text en Copyright: © 2018 Indian Journal of Dermatology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Case Report
Meena, Dilip
Chauhan, Payal
Hazarika, Neirita
Kansal, Naveen Kumar
H Syndrome: A Case Report and Review of Literature
title H Syndrome: A Case Report and Review of Literature
title_full H Syndrome: A Case Report and Review of Literature
title_fullStr H Syndrome: A Case Report and Review of Literature
title_full_unstemmed H Syndrome: A Case Report and Review of Literature
title_short H Syndrome: A Case Report and Review of Literature
title_sort h syndrome: a case report and review of literature
topic Case Report
url 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
work_keys_str_mv AT meenadilip hsyndromeacasereportandreviewofliterature
AT chauhanpayal hsyndromeacasereportandreviewofliterature
AT hazarikaneirita hsyndromeacasereportandreviewofliterature
AT kansalnaveenkumar hsyndromeacasereportandreviewofliterature

Ejemplares similares