Intestinal lymphangiectasia in a patient with infantile systemic hyalinosis syndrome: a rare cause of protein-losing enteropathy

Infantile systemic hyalinosis (ISH) is a rare autosomal recessive disease. Typically, ISH patients present with progressive painful joint contractures, intractable diarrhea, hyperpigmented skin lesions, and perianal fleshy nodules. We report a case of a 19-month-old male child with atypical ISH pres...

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Detalles Bibliográficos
Autores principales: Alreheili, Khalid, AlMehaidib, Ali, Alsaleem, Khalid, Banemi, Mohammad, Aldekhail, Wajeeh, Al-Mayouf, Sulaiman M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: King Faisal Specialist Hospital and Research Centre 2012
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6086646/
https://www.ncbi.nlm.nih.gov/pubmed/22366835
http://dx.doi.org/10.5144/0256-4947.2012.206

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6086646/
https://www.ncbi.nlm.nih.gov/pubmed/22366835
http://dx.doi.org/10.5144/0256-4947.2012.206

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