STT3B-congenital disorder of glycosylation

STT3B-CDG is a form of congenital disorders of N-linked glycosylation characterized by intrauterine growth retardation, microcephaly, failure to thrive, developmental delay, intellectual disability, hypotonia, seizures, optic nerve atrophy and respiratory difficulties. Genital abnormalities (micropenis, hypoplastic scrotum, undescended testes) have also been reported. STT3B-CDG is caused by mutations in the gene STT3B (3p24.1).

Also known as: CDG syndrome type IX, CDG-Ix, CDG1X, STT3B-CDG, STT3B-congenital disorder of glycosylation, carbohydrate deficient glycoprotein syndrome type IX, congenital disorder of glycosylation type 1x, congenital disorder of glycosylation type IX

0 clinical trials for this condition and its sub-types, 0 tagged with STT3B-congenital disorder of glycosylation itself.