autosomal recessive disease pseudo-TORCH syndrome https://www.malacards.org/card/pseudo_torch_syndrome_1 SCTID:722390006 microcephaly-intracranial calcification-intellectual disability 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. OMIMPS:251290 microcephaly intracranial calcification pseudo-TORCH syndrome GARD:0012426 congenital intrauterine infection-like syndrome UMLS:C3489725 Baraitser-Brett-Piesowicz syndrome DOID:0050656 band-like calcification with simplified gyration and polymicrogyria MONDO:0009626 Orphanet:1229 BLC-PMG BLCPMG Baraitser-Reardon syndrome microcephaly - intracranial calcification - intellectual disability Baraitser Brett Piesowicz syndrome MEDGEN:483678 bilateral band-like calcification with polymicrogyria