Genetic correlations and clinical value of increased renal echogenicity in fetuses identified by prenatal ultrasonography

Haihong Liu , Yun Wu , Li Cao , Ting Zhou , LiJun Wu

Precision Medical Sciences ›› 2026, Vol. 15 ›› Issue (1) : 35 -41.

PDF (2240KB)
Precision Medical Sciences ›› 2026, Vol. 15 ›› Issue (1) :35 -41. DOI: 10.1002/prm2.70025
ORIGINAL ARTICLE
Genetic correlations and clinical value of increased renal echogenicity in fetuses identified by prenatal ultrasonography
Author information +
History +
PDF (2240KB)

Abstract

To explore the clinical value of prenatal ultrasound suggesting enhanced fetal renal echo, compare the genetic results and pregnancy outcomes, and provide reference for clinical consultation and prognostic evaluation. A total of 163 cases with enhanced fetal renal echo detected by ultrasound were collected. The ultrasound images and basic maternal data were analyzed, the genetic diagnosis results were compared, and the pregnancy outcomes were followed up. Among the 163 cases, 42 cases (25.77%) of genetic abnormalities were detected, including 24 cases (57.14%) of chromosomal abnormalities, among which 17q microdeletion accounted for the highest proportion. The differences in the detection rate of genetic abnormalities and the incidence of adverse pregnancy outcomes between the advanced age group and the non-advanced age group were statistically significant (p < .05). Enhanced fetal renal echo is closely related to genetic abnormalities, especially 17q abnormalities. When the pregnant woman is of advanced age or the fetus is complicated with other ultrasound abnormalities, the risk of genetic abnormalities increases, requiring focused screening and intervention.

Keywords

enhanced fetal renal echo / genetic diagnosis / prenatal ultrasound

Cite this article

Download citation ▾
Haihong Liu, Yun Wu, Li Cao, Ting Zhou, LiJun Wu. Genetic correlations and clinical value of increased renal echogenicity in fetuses identified by prenatal ultrasonography. Precision Medical Sciences, 2026, 15 (1) : 35-41 DOI:10.1002/prm2.70025

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Chen F, Yuan TT, Chen M, et al. Genetic etiology and pregnancy outcome analysis of fetal bilateral renal parenchymal echogenicity enhancement. Prog Obstet Gynecol. 2022; 31(4): 294-296.

[2]

Zhao ZY, Chen X, Lin PW, et al. Prenatal diagnosis and prognostic analysis of 67 fetal cases with increased renal echogenicity. Chin J Birth Health Heredity. 2025; 33(6): 1360-1365.

[3]

Hertenstein CB, Miller KA, Estroff JA, et al. Fetal hyperechoic kidneys: diagnostic considerations and genetic testing strategies. Prenat Diagn. 2024; 44(2): 15.

[4]

Li SL, Luo GY. Prenatal Ultrasonographic Diagnosis of Fetal Malformations. Science Press; 2017: 510-562.

[5]

Gimpel C, Avni FE, Bergmann C, et al. Perinatal diagnosis, management, and follow-up of cystic renal diseases: a clinical practice recommendation with systematic literature reviews. JAMA Pediatr. 2018; 172(1): 74-86.

[6]

Deng LB, Liu Y, Yuan MZ, et al. Prenatal diagnosis and outcome of fetal hyperechogenic kidneys in the era of antenatal next-generationsequencing. Clin Chim Acta. 2022; 528(1): 16-28.

[7]

Li CL, Liu Y, Yang P, et al. Prenatal ultrasonographic diagnosis of fetal renal echogenicity enhancement and analysis of chromosome results. Chin J Ultrasound Med. 2020; 36(5): 448-450.

[8]

Smajlagić D, Lavrichenko K, Berland S, et al. Population prevalence and inheritance pattern of recurrent CNVs associated with neurodevelopmental disorders in 12,252 newborns and their parents. Eur J Hum Genet. 2021; 29(1): 205-215.

[9]

Huang R, Fu F, Zhou H, et al. Prenatal diagnosis in the fetal hyperechogenickidneys: assessment using chromosomal microarray analysis and exome sequencing. Hum Genet. 2023; 142(6): 835-847.

[10]

Jones GE, Mousa HA, Rowley H, Houtman P, Vasudevan PC. Should we offer prenatal testing for 17q12 microdeletion syndrome to all cases with prenatally diagnosed echogenic kidneys? Prenatal findings in two families with 17q12 microdeletion syndrome and review of the literature. Prenat Diagn. 2015; 35(13): 1336-1341.

[11]

Gilboa Y, Perlman S, Pode-Shakked N, et al. Prenatal diagnosis of 17q12 deletion syndrome: from fetal hyperechogenic kidneys to high risk for autism. Prenat Diagn. 2016; 36(11): 1027-1032.

[12]

Liu YN, Zhang SL, Xu CX, et al. Application of chromosomal microarray analysis and whole-exome sequencing in fetal genetic diagnosis. J Weifang Med Univ. 2023; 45(6): 455-457.

[13]

Xin SW, Yang SZ, Fu XH. Analysis of amniotic fluid chromosome karyotype results in elderly pregnant women. Heilongjiang Medicine and Pharmacy. 2025; 48(12): 78-80.

[14]

Qin CY, Han X, Ling Y, et al. Optimization study on prenatal diagnostic strategies based on fetal ultrasonic soft markers and/or minor anatomical abnormalities associated with chromosomal abnormalities[J/OL]. J Hainan Med Univ. 2026: 1-13.

[15]

Li W, Tong LX, Zeng Y, et al. Relationship between placental microcirculation parameters and adverse pregnancy outcomes in patients with hypertensive disorders of pregnancy[J/OL]. Prog Obstet Gynecol. 2026: 1-5.

[16]

Jian WY, Guo DW, Guo MH, et al. Analysis of outpatient multidisciplinary consultation results for 110 fetuses with urinary system developmental abnormalities. Prog Obstet Gynecol. 2019; 28(10): 765-768.

RIGHTS & PERMISSIONS

2026 The Author(s). Precision Medical Sciences published by John Wiley & Sons Australia, Ltd on behalf of Nanjing Medical University Affiliated Cancer Hospital & Jiangsu Cancer Hospital.

PDF (2240KB)

0

Accesses

0

Citation

Detail

Sections
Recommended

/