CHILD syndrome

Orpha code: 139OMIM code: 308050

Definition

A rare developmental defect during embryogenesis characterized by unilateral inflammatory and scaling skin lesions with ipsilateral visceral and limb anomalies.

Disease data
Classification

Disease

Synonyms
CHILD nevus
Wrodzona hemidysplazja ze znamionami w postaci rybiej łuski i wadami kończyn
Znamię CHILD
Congenital hemidysplasia with ichthyosiform erythroderma and limb defects
ORPHA code
139
OMIM code
308050
ICD10 code
Q87.8
ICD11 code
LD24.04

No additional description.

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