Antenatal diagnosis and maternal sirolimus treatment of polyhydramnios, megalencephaly, and symptomatic epilepsy (PMSE) syndrome.

Background: Polyhydramnios, megalencephaly, and symptomatic epilepsy (PMSE) syndrome is a rare autosomal recessive mTORopathy caused by biallelic STE20-related kinase adaptor alpha ( Methods: A gravida 3 para 2 patient presented at 32+2 weeks with medication-refractory preterm labor and severe polyhydramnios. Fetal magnetic resonance imaging (MRI) demonstrated macrocephaly and an enlarged cavum septum pellucidum (CSP). Amniocentesis with microarray revealed homozygosity across the Results: Maternal sirolimus was well tolerated. Amniotic fluid index (AFI) declined from 36.1 to 26.2 cm, head circumference normalized from the 89th to 35th percentile, and CSP diameter decreased from 14.0 to 12.3 mm. A term vaginal delivery produced a 3554 g infant with normocephaly. Cord blood sirolimus level (3.9 mcg/L) approximated maternal level (3.4 mcg/L). Postnatally, sirolimus was continued from day of life 7. The first seizure occurred at 4.5 months, coincident with subtherapeutic trough levels; seizure control was achieved thereafter. At nearly 5 years, the child shows adequate growth but severe global developmental delay typical of PMSE.This case demonstrates the feasibility and pharmacokinetic effectiveness of maternal sirolimus during late gestation, with no identified maternal or fetal adverse consequences in this first case of third-trimester prenatal mTOR inhibition in confirmed PMSE.