Hunter Syndrome Diagnosed by Otorhinolaryngologist

Hunter syndrome is a lysosomal disease characterized by deficiency of the lysosomal enzyme iduronate-2-sulfatase (I2S). It has an estimated incidence of approximately 1 in 1,62,000 live male births. We report a case of Hunter syndrome diagnosed by an otorhinolaryngologist. To our knowledge, this is...

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Detalles Bibliográficos
Autores principales: Hashimoto, Ayako, Kumagai, Tadayuki, Mineta, Hiroyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5971261/
https://www.ncbi.nlm.nih.gov/pubmed/29862106
http://dx.doi.org/10.1155/2018/4252696

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5971261/
https://www.ncbi.nlm.nih.gov/pubmed/29862106
http://dx.doi.org/10.1155/2018/4252696

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