טוען...
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]....
שמור ב:
| הוצא לאור ב: | J Surg Case Rep |
|---|---|
| Main Authors: | , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Oxford University Press
2020
|
| נושאים: | |
| גישה מקוונת: | 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 |
| תגים: |
הוספת תג
אין תגיות, היה/י הראשונ/ה לתייג את הרשומה!
|