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Start free with EleplanFetal alcohol syndrome
ORPHA:1915Malformation syndrome
Also called ARND · Alcohol-related birth defects · Alcohol-related neurodevelopmental disorder · FAS · FASD · Fetal alcohol spectrum disorders · ARBD
What it is
Fetal alcohol syndrome (FAS) is a rare malformation syndrome caused by excessive maternal consumption of alcohol during pregnancy. It is characterized by prenatal and/or postnatal growth deficiency (weight and/or height <10th percentile), a unique cluster of minor facial anomalies (short palpebral fissures, flat and smooth philtrum, and thin upper lip) and severe central nervous system (CNS) abnormalities including microcephaly, and cognitive and behavioral impairment (intellectual disability, deficit in general cognition, learning and language, executive function, visual-spatial processing, memory, and attention).
Key facts
- Prevalence
- >1 / 1000 (South Africa)
- Age of onset
- Antenatal, Neonatal
- Inheritance
- Not applicable
- Classified as
- Malformation syndrome
Prevalence figures describe populations, not individuals, and are often estimates from a single study. Where the figure is an incidence or a birth prevalence, it says so.
Signs and symptoms
Very common80–99%
10Common30–79%
19- Abnormal dermatoglyphics
- Abnormality of immune system physiology
- Anteverted nares
- Atrial septal defect
- Biparietal narrowing
- Epicanthus
- Joint stiffness
- Microdontia
- Micrognathia
- Microphthalmia
- Non-midline cleft of the upper lip
- Posteriorly rotated ears
- Ptosis
- Short nose
- Smooth philtrum
- Strabismus
- Thin upper lip vermilion
- Vertebral segmentation defect
- Visceral angiomatosis
These ranges are how often a sign appears across everyone diagnosed, not a prediction for one person — most people have some of these and not others. Orphanet also records findings that are specifically absent in this disease; those are in the data but not listed here.
ICD-10 codes
Related health topics
Reached through the ICD-10 categories this disease is filed under, so these describe the broader group rather than this disease specifically.
Cross-references
Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.
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