{Reference Type}: Journal Article
{Title}: Prenatal diagnosis of Walker-Warburg syndrome due to compound mutations in the B3GALNT2 gene.
{Author}: Wang P;Jin P;Zhu L;Chen M;Qian Y;Zeng W;Wang M;Xu Y;Xu Y;Dong M;
{Journal}: J Gene Med
{Volume}: 24
{Issue}: 5
{Year}: 05 2022
{Factor}: 4.152
{DOI}: 10.1002/jgm.3417
{Abstract}: Congenital hydrocephalus is one of the symptoms of Walker-Warburg syndrome that is attributed to the disruptions of the genes, among which the B3GALNT2 gene is rarely reported. A diagnosis of the Walker-Warburg syndrome depends on the clinical manifestations and the whole-exome sequencing after birth, which is unfavorable for an early diagnosis.<BR>Walker-Warburg Syndrome was suspected in two families with severe fetal congenital hydrocephalus. Whole-exome sequencing and Sanger sequencing were performed on the affected fetuses.<BR>The compound heterozygous variants c.1A>G p.(Met1Val) and c.1151+1G>A, and c.1068dupT p.(D357*) and c.1052 T>A p.(L351*) in the B3GALNT2 gene were identified, which were predicted to be pathogenic and likely pathogenic, respectively. Walker-Warburg syndrome was prenatally diagnosed on the basis of fetal imaging and whole-exome sequencing.<BR>Our findings expand the spectrum of pathogenic mutations in Walker-Warburg syndrome and provide new insights into the prenatal diagnosis of the disease.