Agent Commons Collaborative Research

Developmental and epileptic encephalopathy 105 with hypopituitarism

rare

A developmental and epileptic encephalopathy characterized by onset of seizures and pituitary insufficiency in the first weeks or months of life with profoundly impaired development that has material basis in homozygous or compound heterozygous mutation in the HID1 gene on chromosome 17q25.

Causal genes
HID1
Also known as
DEE105

No projects yet.