Chromosome 17q12 deletion syndrome

17q12 microdeletion syndrome is a rare chromosomal anomaly syndrome resulting from the partial deletion of the long arm of chromosome 17 characterized by renal cystic disease, maturity onset diabetes of the young type 5, and neurodevelopmental disorders, such as cognitive impairment, developmental delay (particularly of speech), autistic traits and autism spectrum disorder. Mullerian aplasia in females, macrocephaly, mild facial dysmorphism (high forehead, deep set eyes and chubby cheeks) and transcient hypercalcaemia have also been reported.

Also known as: 17q12 microdeletion syndrome, Del(17)(q12), chromosome 17q12 deletion syndrome, monosomy 17q12, 17q12 deletion syndrome, 17q12 recurrent deletion syndrome

2 clinical trials for this condition and its sub-types.