A delayed diagnosis of congenital midline cervical cleft.

Clin Case Rep · 2022 · PMC8908092 · PMID 35310316

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These findings most likely indicate that the discovered mutations are not disease causing; however, they may be significant factors if CMCC is inherited in a polygenic manner. " 10 , 11 , 12 A detailed physical examination of the patient is typically used to make the diagnosis of CMCC.

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