Schinzel-Giedion syndrome

Disease Export to PDF
Name:
Schinzel-Giedion syndrome
Description:
Schinzel-Giedion syndrome (SGS) is an ectodermal dysplasia syndrome chiefly characterized by a distinctive facial dysmorphism, hydronephrosis, severe developmental delay, typical skeletal malformations, and genital and cardiac anomalies.
ORPHAcode:
798
Synonyms:
SGS
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14