Table 1

Proportion of microcephalic infants presenting with other congenital anomalies

Microcephaly,
n (%)*
Central nervous system
 Spina bifida11 (1.4)
 Anencephaly/encephalocoele12 (1.5)
 Congenital hydrocephalus6 (0.8)
 Other42 (5.3)
 Any65 (8.2)
 Eye20 (2.5)
 Ear17 (2.1)
 Orofacial clefts19 (2.4)
Heart
 Critical20 (2.5)
 Non-critical80 (10.1)
 Any89 (11.2)
 Respiratory <5 (<0.6)
 Digestive23 (2.9)
Urinary
 Hypospadias8 (1.0)
 Renal agenesis6 (0.8)
 Other19 (2.4)
 Any32 (4.0)
Skeletal
 Congenital hip dislocation12 (1.5)
 Clubfoot29 (3.7)
 Limbs and digits13 (1.6)
 Skull and face bones16 (2.0)
 Other24 (3.0)
 Any73 (9.2)
Chromosomal
 Down17 (2.1)
 Trisomy 13 or 1811 (1.4)
 Autosomal or sex-linked11 (1.4)
 Other10 (1.3)
 Any47 (5.9)
 Lethal‡50 (6.3)
 Any defect§295 (37.2)
 Isolated microcephaly499 (62.8)
 Total794 (100)
  • *Categories are not mutually exclusive, and microcephalic neonates with two or more other anomalies appear more than once.

  • †Fewer than five defects cannot be reported, to comply with data confidentiality requirements.

  • ‡Potentially lethal defects, including anencephaly, encephalocoele, omphalocoele, diaphragmatic hernia, lung agenesis, critical heart defects, renal agenesis, osteogenesis imperfecta, osteochondroplasia, trisomy 13 and trisomy 18.

  • §Includes all defects in the table plus the ranges 740–742.0, 742.2–759, Q00–Q01.9 and Q03–Q99 of the International Classification of Diseases.