(Q9390596)

English

pseudo-TORCH syndrome

autosomal recessive disease that is characterized by congenital microcephaly, intracranial calcifications, severe developmental delay, severe developmental delay, simplified gyration and polymicrogyria

  • band-like calcification with simplified gyration and polymicrogyria
  • Baraitser-Brett-Piesowicz syndrome
  • Baraitser-Reardon syndrome
  • Pseudo-Torch Syndrome
  • pseudo-TORCH syndrome type 1
  • Microcephaly-intracranial calcification-intellectual disability syndrome
  • BLCPMG
  • Bilateral band-like calcification with polymicrogyria
  • pseudo-TORCH syndrome 1
  • BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA; BLCPMG
  • Congenital intrauterine infection-like syndrome
  • BLC-PMG

Statements

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