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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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| Publicat a: | Ann Saudi Med |
|---|---|
| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
King Faisal Specialist Hospital and Research Centre
2012
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6086646/ https://ncbi.nlm.nih.gov/pubmed/22366835 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5144/0256-4947.2012.206 |
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