Skip to main content
Fig. 2 | BMC Neurology

Fig. 2

From: Whole-exome sequencing identifies homozygous mutation in TTI2 in a child with primary microcephaly: a case report

Fig. 2

Clinical phenotype of the patient with TTI2 mutation. a-b axial T2 images and c axial Flair image of brain magnetic resonance imaging (MRI) from the boy at 1 year of age. Small supratentorial ventriculomegaly and minor mixed diffuse cortical atrophy can be observed. d-f Growth curves for head circumference (d), weight (e) and height (f) from birth to the age of two years old. Blue line indicate percentile from age and sex matched controls

Back to article page

BMC Neurology

ISSN: 1471-2377

Contact us