U01.15.005 Fetal alcohol syndrome

Learning Objectives

Master the clinical presentation and neurobiological basis of Fetal Alcohol Syndrome (FAS). Identify high-yield facial dysmorphisms and structural brain defects for the USMLE Step 1.


1. Pathogenesis and Etiology

Fetal Alcohol Syndrome is a leading preventable cause of intellectual disability in the United States, occurring secondary to maternal alcohol consumption during pregnancy.

Mechanism Clinical Impact
Cellular Migration Impaired migration of neuronal and glial cells.
Structural Defect Holoprosencephaly (failure of the prosencephalon to divide) may occur in severe cases.
Development Leads to microcephaly and significant developmental delay.

2. Classic Facial Dysmorphisms

The diagnosis is often clinical, based on a specific constellation of facial features that are high-yield for board exams.

Feature Description
Philtrum Smooth philtrum (loss of the vertical groove between the nose and upper lip).
Upper Lip Thin vermillion border (very thin upper lip).
Eyes Small palpebral fissures (short horizontal eye openings).
Nose Flat nasal bridge.

3. Associated Systemic Defects

Beyond the face and brain, alcohol is a potent teratogen affecting multiple organ systems.

System Associated Defect
Cardiac Heart defects (e.g., VSD, ASD, or Tetralogy of Fallot).
Skeletal Limb dislocation and joint anomalies.
Management Supportive care; multidisciplinary approach for developmental needs.

Activity:


High-Yield Clinical Pearls:

  • The Smooth philtrum: This is often the most specific physical clue mentioned in board vignettes.
  • Holoprosencephaly: If a question mentions “failure of the brain to divide into two hemispheres,” think of alcohol or Patau syndrome (Trisomy 13).
  • Intellectual Disability: Remember that alcohol is the #1 preventable cause, while Fragile X is the #1 inherited cause, and Down Syndrome is the #1 genetic/chromosomal cause.

Activity: