MNX1 GENE ANALYSIS IN CURRARINO SYNDROME
Currarino syndrome caused by disease-causing variants in the MNX1 gene is a congenital disorder characterized by agenesis of the sacrum, anal atresia and a pre-sacral mass. Addition clinical manifestations include tethered cord and/or lipoma of the conus. The disorder is transmitted in an autosomal dominant manner with variable expressivity.
The laboratory participates in the European Molecular Genetics Quality Network (EMQN) sequencing scheme.
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