WAGR Syndrome - Phenotip

WAGR Syndrome Relevant markers:

Borderline ventriculomegaly (10-12 mm)Absent cavum septum pellucidum (CSP)OligohydramniosNephromegaly

Parents markers:

Agenesis of corpus callosum (ACC)Intrauterine growth retardation (IUGR/SGA/FGR)

Incidence:

1/500000 — 1/1000000

Inheritance mode:

AD, Sporadic (new mutation)

Other online databases:

References:

2015

Case Rep Obstet Gynecol

Case report