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Waardenburg-Shah syndrome (WS type IV): a rare case from Pakistan
Waardenburg-Shah syndrome is a rare autosomal recessive [AR] inherited disorder characterized by the presence of Hirschsprung’s disease with a high likelihood of aganglionic megacolon, due to which the mortality is high. The management of the condition involves surgical intervention for the removal...
Tallennettuna:
| Julkaisussa: | Perioper Med (Lond) |
|---|---|
| Päätekijät: | , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2020
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6979113/ https://ncbi.nlm.nih.gov/pubmed/31998473 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13741-019-0135-x |
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