A recent theory about the basis for fragile X syndrome is now validated in a mouse model. The findings point the way to treatment options targeting group 1 metabotropic glutamate receptors.
Light and electron microscopy of fetal testes at 16 and 22 weeks of gestation, following prenatal diagnosis of the Fragile X Syndrome, revealed that the morphogenesis of the macroorchidism begins ...
Fragile X syndrome is caused by an alteration to a gene ... “Physical features include a long face, large or prominent ears, and flat feet – which usually become more noticeable in young ...
Fragile X syndrome is caused by an alteration to a gene ... Genetically, women with the condition face a 50% probability of passing the disorder to their offspring, whereas affected males will ...