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Bowen-Conradi syndrome

Disease Export to PDF
Name:
Bowen-Conradi syndrome
Description:
A rare developmental defect during embryogenesis characterized by moderate to severe prenatal and postnatal growth retardation, microcephaly, a distinctive facial appearance, profound psychomotor delay, hip and knee contractures and rockerbottom feet.
ORPHAcode:
1270
Synonyms:
Bowen syndrome, Hutterite type
XREF(s):
Orphanet
OMIM
MeSH
ICD-10
Analyte(s):
EMG1
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14