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Fig. 3 | BMC Medical Genetics

Fig. 3

From: A novel frameshift mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome using targeted exome sequencing

Fig. 3

Systemic clinic features of affected family members with Axenfeld-Rieger syndrome. No microdontia was observed for I-2 because of a dental implant (a). Apparent microdontia for II-1 and II-2 (b and c). Dental panoramic radiography for II-1 (d), and II-2 had similar dental panoramic radiography. Umbilical defect (redundant periumbilical skin) for II-2 (e). All three patients exhibited the same sign when they underwent general physical examination. Broad nasal bridge of II-1 and II-2 (f and g)

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