C154618Level 6
Lethal Neonatal Rigidity and Multifocal Seizure Syndrome
**Semantic type:** Disease or Syndrome
**Definition:** A rare, autosomal recessive genetic disorder caused by mutations in the BRAT1 gene that is characterized by microcephaly, neonatal onset of multifocal epilepsy, developmental arrest, and early death.
**Synonyms:** - RMFSL
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