Prenatal Diagnosis of KBG Syndrome: Phenotypic and Genotypic Features of 12 Fetal Cases With the Disorder

Increased NT and mild ventriculomegaly are two common sonographic features of fetal KBGS. Prenatal diagnosis of KBGS can be achieved with ultrasound and comprehensive molecular testing.

Authors

Xiangyi Jing (ORCID: https://orcid.org/0000-0001-7703-723X)
Qiuxia Yu (ORCID: https://orcid.org/0000-0003-4621-7523)
Dong‐Zhi Li (ORCID: https://orcid.org/0000-0002-4583-6800)
Li Zhen
Zhi‐Qing Xiao

Institutions

Guangzhou Medical University (CN)

Publication Details

Journal: Prenatal Diagnosis
Published: 2025-02-26
DOI: https://doi.org/10.1002/pd.6768
Citations: 1
Primary Topic: Genomics and Rare Diseases
Type: article
Field-Weighted Citation Impact: 1.82

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article

Prenatal Diagnosis of KBG Syndrome: Phenotypic and Genotypic Features of 12 Fetal Cases With the Disorder

Xiangyi Jing, Qiuxia Yu, Dong‐Zhi Li, Li Zhen et al.

Feb 26, 2025

1 citations

Prenatal Diagnosis

Genomics and Rare Diseases

1.82

article

Prenatal Diagnosis of KBG Syndrome: Phenotypic and Genotypic Features of 12 Fetal Cases With the Disorder

Xiangyi Jing, Qiuxia Yu, Dong‐Zhi Li, Li Zhen, Zhi‐Qing Xiao

February 26, 2025article en

1 citations

Abstract

Increased NT and mild ventriculomegaly are two common sonographic features of fetal KBGS. Prenatal diagnosis of KBGS can be achieved with ultrasound and comprehensive molecular testing.

Prenatal DiagnosisVol. 45(4)

Guangzhou Medical University (CN)

Openalex Percentile: Top 18%

Genomics and Rare Diseases

1.82

DOI Open Access PDF OpenAlex

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Prenatal Diagnosis of KBG Syndrome: Phenotypic and Genotypic Features of 12 Fetal Cases With the Disorder — Xiangyi Jing, Qiuxia Yu, et al. · Prenatal Diagnosis (2025) | TGRS Research Map | TGRS