{Reference Type}: Case Reports
{Title}: Novel variants identified in five Chinese families with Joubert Syndrome: a case report.
{Author}: Fang L;Wang L;Yang L;Xu X;Pei S;Wu ;
{Journal}: BMC Med Genomics
{Volume}: 16
{Issue}: 1
{Year}: 2023 09 21
{Factor}: 3.622
{DOI}: 10.1186/s12920-023-01669-7
{Abstract}: Joubert syndrome (JS) is a group of rare ciliopathies, mainly characterized by cerebellar dysplasia representing the "molar tooth sign (MTS)" on neuroimaging, hypotonia, and developmental delay. Having a complicated genotype-phenotype correlation due to its rich genetic heterogeneity, JS is usually combined with other organic defects affecting the retina, kidney, and liver. This report aimed to present new cases and novel variants of JS.<BR>Five unrelated patients who were diagnosed with JS, with or without typical clinical characteristics, received integrated examinations, including whole-exome sequencing (WES) and Sanger sequencing. We identified nine pathogenic variants in the TCTN2, CPLANE1, INPP5E, NPHP1, and CC2D2A genes.<BR>Four novel pathogenic mutations in the TCTN2, CPLANE1, and INPP5E genes were reported. The findings broadened the genotypic spectrum of JS and contributed to a better understanding of genotype-phenotype correlation.