Table 3.
Variable | TOF (n = 66) | Referent (n=75) | P value* |
---|---|---|---|
n (%) | |||
Any abnormality | 28 (42) | 6 (8) | <0.001 |
Focal or multifocal abnormality | 24 (36) | 1 (1) | <0.001 |
Focal infarction or atrophy | 4 (6) | 0 | 0.046 |
Brain mineralization/iron deposit | 21 (32) | 1 (1) | <0.001 |
Diffuse abnormality | 2 (3) | 1 (1) | 0.60 |
Myelination delay | 0 | 0 | - |
Ventriculogealy | 1 (2) | 0 | 0.47 |
Abnormal T2 hyperintensities | 1 (2) | 1 (1) | 1.0 |
Generalized abnormality | 1 (2) | 0 | 0.47 |
Developmental abnormality | 6 (9) | 4 (5) | 0.52 |
Major malformation† | 1 (2) | 0 | 0.47 |
Minor malformation‡ | 5 (8) | 4 (5) | 0.73 |
TOF = tetralogy of Fallot.
Determined by Fisher’s exact tests.
The major malformation is hypoplasia in the right cerebellar hemisphere and Dandy-Walker spectrum anomaly.
Minor malformations include agenesis of the corpus and partial anterior absence of corpus callosum (no other findings of holoprosencephaly), arachnoid cyst, subependymal nodular heteropia (right parietal white matter), absent splenium of corpus callosum (not agenesis), and mildly dysmorphic ventricles in TOF group; and Chiari malformation and developmental venous anomaly in right parietal lobe in referent group.