Reported rate per 105per annum (95% CI)† | |
Children aged <15 years at diagnosis (total population) | 0.58 (0.46 to 0.71) |
Non-Indigenous population | 0.18 (0.12 to 0.27) |
Indigenous population (p<0.001) | 8.11 (6.19 to 10.44) |
Children aged <5 years at diagnosis (total population) | 1.14 (0.87 to 1.47) |
Non-Indigenous population | 0.37 (0.22 to 0.59) |
Indigenous population (p<0.001) | 14.60 (10.22 to 20.22) |
Clinical characteristics(n = 92)*, n (%) | |
Sex (male) | 49 (53.3) |
Gestation <37 weeks (n = 84) | 30 (35.7) |
Mean (SD) gestation (weeks) | 37.4 (2.68) |
Birth weight <2.5 kg (n = 82) | 53 (64.6) |
Mean (SD) birth weight (kg) | 2.36 (0.53) |
Median age at FAS diagnosis in years (range) | 3.26 (newborn to 11.9) |
Diagnosis at birth | 6 (6.5) |
Diagnosis at age <1 year | 22 (23.9) |
Diagnosis at age <2 years | 36 (39.1) |
Diagnosis at age <5 years | 58 (63) |
Diagnostic features | |
Facial features (any) | 92 (100) |
Smooth philtrum | 89 (96.7) |
Thin upper lip | 87 (94.6) |
Short palpebral fissure | 56 (60.9) |
All of the above features | 53 (57) |
Growth restriction (n = 91) | 51 (56.0) |
Normal | 40 (44.0) |
Prenatal only | 22 (24.2) |
Postnatal only | 18 (19.8) |
Both prenatal and postnatal | 11 (12.1) |
CNS structural abnormality (any) | 50 (54.3) |
Microcephaly (HC <3rd percentile) alone | 45 (48.9) |
Microcephaly plus other structural defect‡ | 4 (4.3) |
Structural defect alone (agenesis corpus callosum) | 1 (1.1) |
CNS dysfunction | 79 (85.9) |
Speech/language disorder | 55 (59.8) |
Fine motor delay | 46 (50.0) |
Intellectual impairment | 45 (48.9) |
Behavioural problems | 45 (48.9) |
Gross motor delay | 33 (35.9) |
Poor coordination | 36 (39.1) |
Emotional problems | 26 (28.3) |
Abnormal muscle tone | 20 (21.7) |
Abnormal deep tendon reflexes | 12 (13) |
Refractory error | 7 (7.6) |
Seizure disorder | 6 (6.5) |
Tremor | 6 (6.5) |
Sensorineural hearing loss | 5 (5.4) |
Visual impairment | 4 (4.3) |
Nystagmus | 2 (2.2) |
*n = 92 unless otherwise stated.
†Rates calculated using population estimates for Aboriginal and Torres Strait Islander and non-Indigenous populations from the Australian Bureau of Statistics for the years of the study. p<0.001 indicates the difference in reported rates between Indigenous and non-Indigenous children in each age group.
‡Structural defects of the central nervous system (CNS) included agenesis of the corpus callosum, absent pituitary stalk, thalamic cyst, cerebral atrophy, subcortical gliosis, delayed white matter myelination and abnormal cerebellum.
HC, head circumference.