Fryns syndrome

Fryns syndrome (FS) is a multiple congenital anomaly syndrome characterized by dysmorphic facial features, congenital diaphragmatic hernia, pulmonary hypoplasia, and distal limb hypoplasia, in addition to variable expression of additional malformations.

Also known as: Fryns syndrome, diaphragmatic hernia-abnormal face-distal limb anomalies syndrome, FRNS, Moerman Van den Berghe Fryns syndrome, diaphragmatic hernia, abnormal face, and distal limb anomalies

1 clinical trial for this condition and its sub-types, 1 tagged with Fryns syndrome itself.