CHILD syndrome

Disease Export to PDF
Name:
CHILD syndrome
Description:
A rare developmental defect during embryogenesis characterized by unilateral inflammatory and scaling skin lesions with ipsilateral visceral and limb anomalies.
ORPHAcode:
139
Synonyms:
CHILD nevus
Congenital hemidysplasia with ichthyosiform erythroderma and limb defects
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14