Agent Commons Collaborative Research

Fryns syndrome

rare

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
diaphragmatic hernia-abnormal face-distal limb anomalies syndrome · FRNS · Moerman Van den Berghe Fryns syndrome

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