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Peer-reviewed veterinary case report

DVL2 gene variant linked to flat face and kinked tail in bulldogs

By Niskanen, Julia E et al.·Published in Human genetics·2021·Department of Medical and Clinical Genetics·View original on PubMed

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Original publication title: Canine DVL2 variant contributes to brachycephalic phenotype and caudal vertebral anomalies.

Species:
dog

Plain-English summary

A study found that a genetic variant in the DVL2 gene is linked to physical traits in English Bulldogs, French Bulldogs, and Boston Terriers, including a kinked tail and a flat face. This variant may also be associated with health issues like breathing problems and heart defects. Researchers examined 1,954 dogs from various breeds and confirmed that this genetic change contributes to the distinctive "bulldog type" appearance and certain spinal deformities. Understanding this genetic link can help owners be more aware of potential health risks in these breeds.

People also search for: bulldog tail problems · French Bulldog breathing issues · Boston Terrier heart defects

Abstract

A frameshift deletion variant in the Wnt pathway gene dishevelled 2 (DVL2) is associated with a truncated, kinked tail ("screw tail") in English Bulldogs, French Bulldogs and Boston Terriers. These breeds are also characterized by distinctive morphological traits, including a wide head, flat face and short-limbed dwarfism, which are characteristic of Robinow syndrome in humans, caused by defects in genes such as DVL1 and DVL3. Based on these phenotypic and genetic similarities, it has previously been hypothesized that the canine DVL2 variant results in a syndromic phenotype called the Robinow-like syndrome. In our study, we investigated the distribution of the DVL2 variant in 1954 dogs from 15 breeds, identifying breeds with allele variation and enabling the dissection of the genotype-phenotype correlation for the first time. With CT examinations in American Staffordshire Terriers, we confirmed that the DVL2 allele is associated with caudal vertebral malformations and a brachycephalic phenotype. We also hypothesize that the variant may be linked to additional health conditions, including brachycephalic obstructive airway syndrome and congenital heart defects. Altogether, our study strengthens the role of DVL2 as one of the contributors to the "bulldog type" morphology and features on the spectrum of human Robinow syndrome.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/33599851/