Biliary, Renal, Neurological, and Skeletal syndrome in a Chinese boy

Biliary, Renal, Neurological, and Skeletal syndrome (BRENS syndrome) is a very rare ciliopathy caused by variants in the TTC26 (OMIM 617453) gene. There are only a few case reports of BRENS syndrome in the literature. We report here a Chinese case of BRENS syndrome who presented with kidney, neurological, skeletal, and other features. It is the first description of BRENS syndrome without biliary involvement. Gene testing revealed three novel compound heterozygous variants in the TTC26 gene, c.1069 + 5G > A in one allele from the mother and c.511A > G (p.Ile171Val) and c.1099T > C (p.Ser367Pro) in another allele from the father. We suggest that patients with BRENS syndrome may exhibit variable phenotypes.

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Publication Details

Journal
Pediatric Nephrology
Published
2024-11-08
DOI
https://doi.org/10.1007/s00467-024-06591-3
Citations
1
Primary Topic
Genetic and Kidney Cyst Diseases
Type
article
Field-Weighted Citation Impact
0.55
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article

Biliary, Renal, Neurological, and Skeletal syndrome in a Chinese boy

Lijuan Ma, Xiaoyu Li, Hongwen Zhang, Yang Wu
1 citations
Pediatric Nephrology
Genetic and Kidney Cyst Diseases
0.55
article

Biliary, Renal, Neurological, and Skeletal syndrome in a Chinese boy

Lijuan Ma, Xiaoyu Li, Hongwen Zhang, Yang Wu
article en
1 citations

Abstract

Biliary, Renal, Neurological, and Skeletal syndrome (BRENS syndrome) is a very rare ciliopathy caused by variants in the TTC26 (OMIM 617453) gene. There are only a few case reports of BRENS syndrome in the literature. We report here a Chinese case of BRENS syndrome who presented with kidney, neurological, skeletal, and other features. It is the first description of BRENS syndrome without biliary involvement. Gene testing revealed three novel compound heterozygous variants in the TTC26 gene, c.1069 + 5G > A in one allele from the mother and c.511A > G (p.Ile171Val) and c.1099T > C (p.Ser367Pro) in another allele from the father. We suggest that patients with BRENS syndrome may exhibit variable phenotypes.

Pediatric NephrologyVol. 40(4)
Peking University (CN), Yinchuan First People's Hospital (CN), Peking University First Hospital (CN)
Good health and well-being
Openalex Percentile: Top 25%
Genetic and Kidney Cyst Diseases
0.55
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