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[Clinical and Genetic Analysis of a Novel CHD4 Gene Variant in a Chinese Patient with Sifrim-Hitz-Weiss Syndrome]

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Specialty Genetics
Date 2021 Jan 10
PMID 33423261
Citations 2
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Abstract

Objective: To explore the genotype-phenotype correlation of a case with Sifrim-Hitz-Weiss syndrome (SIHIWES) caused by a novel CHD4 gene variant.

Methods: Genomic DNA was extracted from peripheral blood samples of the patient and her parents. Whole-exome sequencing (WES) was carried out for the patient.Suspected variant was verified by Sanger sequencing.

Results: The proband, a 2-year-old Chinese girl, presented with global developmental delay, intellectual disability, distinctive facial features and multiple congenital anomalies. Her prenatal manifestations included increased nuchal thickness, cranial and facial anomalies, and decreased fetal movement. WES has identified a novel variant in the CHD4 gene, namely NM_001273:c.2989C>G (p.Leu997Val) (GRCh37/hg19).Comparison of her phenotype with previously reported SIHIWES cases suggested that our patient's prenatal presentations were unreported before, with novel features including funduscopic anomaly, facial dysmorphisms such as asymmetrical ears, drooping eyelid, long philtrum and downturned mouth.

Conclusion: Above findings have expanded the mutational spectrum of the CHD4 gene and revealed novel phenotypes in Chinese patients with SIHIWES.

Citing Articles

Sifrim-Hitz-Weiss/CHD4-related syndrome: A new case report.

Zhang B, Cheng M, Fan L, Gong C Pediatr Investig. 2023; 7(2):137-139.

PMID: 37324594 PMC: 10262901. DOI: 10.1002/ped4.12357.


A Novel Frameshift Variant Leading to Sifrim-Hitz-Weiss Syndrome in a Proband with a Subclinical Familial t(17;19) and a Large dup(2)(q14.3q21.1).

Da Silva J, Oliva-Teles N, Tkachenko N, Fino J, Marques M, Fortuna A Biomedicines. 2023; 11(1).

PMID: 36672520 PMC: 9855399. DOI: 10.3390/biomedicines11010012.