Chromosomal Abnormalities in Syndromic Orofacial Clefts: Report of Three Children

Figure 1

Proband 1 with Emanuel syndrome: (a) phenotype with unilateral left ptosis, microretrognathia, (b) T2 weighted magnetic resonance imaging of brain (sagittal) showing hypoplastic body of corpus callosum (arrow), (c) karyotype and ideogram showing marker chromosome, and (d) karyotype and ideogram of mother showing t(11; 22)(q24; q12).