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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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