Wiedemann-Rautenstrauch syndrome

Disease Export to PDF
Name:
Wiedemann-Rautenstrauch syndrome
Description:
A rare multiple congenital anomalies/dysmorphic syndrome characterized by marked prenatal and postnatal growth retardation, decreased subcutaneous fat, hypotrichosis, relative macrocephaly and an unusual face. Mild to moderate intellectual disability is common.
ORPHAcode:
3455
Synonyms:
Neonatal progeroid syndrome
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14