Hyaline Fibromatosis Syndrome: A Rare Inherited Disorder

Hyaline fibromatosis syndrome (HFS) is rare autosomal recessive disease characterized by the deposition of amorphous hyaline material in skin and visceral organs. It represents a disease spectrum with infantile systemic hyalinosis (ISH) being the severe form and juvenile hyaline fibromatosis (JHF) b...

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Detalles Bibliográficos
Autores principales: Mantri, Meeta Dipak, Pradeep, Mahajan M, Kalpesh, Patil O, Pranavsinh, Raj J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
E-IJD Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5029258/
https://www.ncbi.nlm.nih.gov/pubmed/27688461
http://dx.doi.org/10.4103/0019-5154.190129

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5029258/
https://www.ncbi.nlm.nih.gov/pubmed/27688461
http://dx.doi.org/10.4103/0019-5154.190129

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