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HEC syndrome

ORPHA:2119· ICD-10 Q87.8

Definition

A rare syndromic cardiac disease characterized by communicating hydrocephalus, endocardial fibroelastosis, and congenital cataracts. A history of upper respiratory infection in the mother during the first trimester of pregnancy and polyhydramnios in the third trimester has been associated. No evidence of toxoplasmosis, rubella, cytomegalovirus, herpes simplex virus, syphilis, and galactosemia is reported. There have been no further descriptions in the literature since 1995.

Prevalence
<1 / 1 000 000
Inheritance
Unknown
Age of onset
Neonatal