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. The disease is MONDO_0009626 (pseudo-TORCH syndrome). 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.