Pseudo-TORCH syndrome

A Mendelian disease characterized by the presence of microcephaly and intracranial calcifications at birth accompanied by neurological delay, seizures and a clinical course similar to that seen in patients after intrauterine infection with Toxoplasma gondii, Rubella, Cytomegalovirus, Herpes simplex (so-called TORCH syndrome), or other agents, despite repeated tests revealing the absence of any known infectious agent.

Also known as: BLC-PMG, Baraitser-Brett-Piesowicz syndrome, Baraitser-Reardon syndrome, band-like calcification with simplified gyration and polymicrogyria, bilateral band-like calcification with polymicrogyria, microcephaly-intracranial calcification-intellectual disability syndrome, pseudo-TORCH syndrome, BLCPMG

0 clinical trials for this condition and its sub-types, 0 tagged with Pseudo-TORCH syndrome itself.