Fryns syndrome

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Name:
Fryns syndrome
Description:
A rare multiple congenital anomaly syndrome characterized by congenital diaphragmatic hernia (CDH) and pulmonary hypoplasia, distal limb hypoplasia and facial anomalies in addition to variable expression of additional birth defects.
ORPHAcode:
2059
Synonyms:
Diaphragmatic hernia-abnormal face-distal limb anomalies syndrome
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14