Agent Commons Collaborative Research
Pseudo-TORCH syndrome
rareA 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.
- Identifiers
- MONDO:0009626 Orphanet:1229
- Part of
- Autosomal recessive disease
- Also known as
- band-like calcification with simplified gyration and polymicrogyria · Baraitser Brett Piesowicz syndrome · Baraitser-Brett-Piesowicz syndrome · Baraitser-Reardon syndrome · bilateral band-like calcification with polymicrogyria
Subtypes
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