Article

A case of prenatal diagnosis of 16q24.3 microdeletion KBG syndrome and review of the literature

2021-07-20

Abstract excerpt

Diagnosis of KBGS due to a high risk identified by early Down's syndrome screening has not been reported in previous studies, and the prominent KBGS phenotype and absence of specificity on early ultrasound examination also pose a challenge for genetic diagnosis.

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Literature Corpus work: 56317c67-40cc-5242-958a-de7fc46d1a6b
DOI: 10.22541/au.162675256.68454481/v1

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