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Aminopterin/methotrexate embryofetopathy

ORPHA:1908· ICD-10 Q86.8

Definition

A syndrome of developmental anomalies characterized by growth deficiency, facial dysmorphism and skull, limb and neural defects secondary to maternal exposure to aminopterin or methotrexate (MTX) during pregnancy.

Prevalence
<1 / 1 000 000
Inheritance
Not applicable
Age of onset
Antenatal, Neonatal