C98929Level 5
Fetal Retinoid Syndrome
**Semantic type:** Congenital Abnormality|Disease or Syndrome
**Definition:** A teratogenic disorder observed in a newborn or child of a mother who was exposed to retinoids during pregnancy. Manifestations include growth delay, skull, facial, heart, and central nervous system malformations.
**Synonyms:** - Fetal Isotretinoin Syndrome - Retinoic Acid Embryopathy - Retinoic Acid Embryopathy
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