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Figure 2 | Molecular Cytogenetics

Figure 2

From: Clinical and molecular evaluations of siblings with “pure” 11q23.3-qter trisomy or reciprocal monosomy due to a familial translocation t (10;11) (q26;q23.3)

Figure 2

Clinical features of the patients. Left panel: III1-3: The craniofacial features of trisomy 11q23.3-q25 patients. Multiple facial dysmorphisms including microcephaly, brachycephaly, plagiocephaly and short philtrum are shown. III-4: The craniofacial features of the patient with Jacobsen syndrome. Her craniofacial features include facial asymmetry, low set ears, blepharophimosis, ptosis and epicanthal folds, broad nasal bridge, a thin upper lip. Right Panel: The brain MRI of 11q23.3-q25 trisomy patients. The brain MRI indicates the small pituitary gland and empty sella, and the bilateral parietal sulcus deepening was observed.

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Molecular Cytogenetics

ISSN: 1755-8166