ArticleClinical case reports2022
A case of prenatal diagnosis of 16q24.3 microdeletion KBG syndrome and review of the literature.
Article in Clinical case reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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Who cites it
1 citing paper in PubMed.
- A case of prenatal diagnosis of 16q24.3 microdeletion KBG syndrome and review of the literature.Clinical case reports · 2022Article
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Authors and funding
5 authors.
Funding
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Abstract
Here we report a case of a 16q24.3 microdeletion KBG syndrome (KBGS) in a fetus. The absence of a well-defined phenotype poses a challenge for genetic diagnosis. This report demonstrated that the high-risk chromosome 21 trisomy could be the first manifestation of KBGS, as observed in this case.
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