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Ultrashort-segment Hirschsprung disease in a 4-year-old female
Hirschsprung disease (HSCR) is characterized by the absence of neuronal ganglion cells in a distal portion of the intestinal tract [1]. In 1691, Frederick Ruysch described the disease as congenital megacolon. HSCR-associated congenital anomalies have been reported in 5–32% of affected patients [2]....
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| 出版年: | J Surg Case Rep |
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| 主要な著者: | , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Oxford University Press
2020
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7524601/ https://ncbi.nlm.nih.gov/pubmed/33024529 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/jscr/rjaa320 |
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