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. Author manuscript; available in PMC: 2013 Mar 22.
Published in final edited form as: Am J Med Genet A. 2010 Nov;152A(11):2854–2860. doi: 10.1002/ajmg.a.33686

FIG. 1.

FIG. 1

Photographs of individuals with EYA1 contiguous gene deletions. A: Patient 1 at the age of 15 months, with facial asymmetry, left-sided microphthalmos with iris coloboma, cup-shaped, simplified asymmetric ears, bilateral preauricular pits, bilateral branchial cleft fistulae, and micrognathia. B: Patient 2 at the age of 34 months, with frontal bossing, small, low set ears with bilateral preauricular pits, midfacial hypoplasia, and micrognathia. C: Patient 3 at the age of 7.5 years, with bilateral preauricular ear pits, small right preauricular tag, and large anteriorly protruding ears with cupped helices.