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pro vyhledávání: '"Nupur Pandya"'
Publikováno v:
Medical Journal of Dr. D.Y. Patil Vidyapeeth, Vol 17, Iss Suppl 1, Pp S213-S215 (2024)
KBG syndrome is a rare genetic disorder manifested by craniofacial dysmorphism, skeletal abnormalities, short stature, and developmental delay. The anesthetic management may be challenging due to associated craniofacial and other skeletal abnormaliti
Externí odkaz:
https://doaj.org/article/1fd9fe42ea5d4f5fbb12ca9f7ec92604
