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Figure 1 | Molecular Cytogenetics

Figure 1

From: Clinico-radiological and molecular characterization of a child with ring chromosome 2 presenting growth failure, microcephaly, kidney and brain malformations

Figure 1

Patient at 5 years of age. (A) Lateral and (B) frontal views of the face of the boy at 5 years of age show medial eyebrow flare, wide nasal bridge, hypertelorism, epicanthal folds, broad nasal tip with prominent columella, long philtrum, thin upper lip, short neck. Hands (C) and feet (D) pictures demonstrate small hands and feet with clinodactyly and brachydactyly and left clubfoot.

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