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Autor:
Rasha A. Al-Youzbaki, Emad Hazim Mahmoud, Zahraa A. Alsubaihawi, Mohammed A. Almeran, Saja A. Albanaa, Samer S. Hoz
Publikováno v:
Romanian Neurosurgery, Vol 37, Iss 1 (2023)
Introduction: Currarino Syndrome (CS) is a rare entity characterized by a triad of sacral agenesis, anorectal malformations, and pre-sacral masses. CS is typically diagnosed during the first decade of life. Case Description: We present a rare case
Externí odkaz:
https://doaj.org/article/c9b27ff94fe9475893ff0395ac0d946f