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. Author manuscript; available in PMC: 2016 Jan 31.
Published in final edited form as: Cardiol Young. 2014 Feb 11;25(2):338–347. doi: 10.1017/S1047951114000031

Table 3.

Structural magnetic resonance imaging findings of adolescents with tetralogy of Fallot and referents.

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.