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• W2006075485 abstract "Holoprosencephaly (HPE) is the most common disorder of the developing forebrain in humans, and is characterized by failed or incomplete cleavage of the cerebral hemispheres and deep brain structures. HPE includes wide phenotypic variability, with a continuum of both brain and craniofacial anomalies. While “classic” eye findings, including the spectrum of midline anomalies ranging from cyclopia to hypotelorism, as well as chorioretinal coloboma and microphthalmia, have been frequently described in patients with HPE, other subtle eye anomalies may also occur. In our study we prospectively analyzed a small cohort of 10 patients in whom we identified mutations in SHH, SIX3, ZIC2, or FGF8, the latter of which is a very recently described HPE-associated gene. We found that 9 of 10 patients had at least two ophthalmologic anomalies, including refractive errors, microcornea, microphthalmia, blepharoptosis, exotropia, and uveal coloboma. These findings contribute to the understanding of the phenotypic variability of the HPE spectrum, and highlight findings in one medically important but often incompletely investigated system. Published 2011. This article is a U.S. Government work and is in the public domain in the USA." @default.
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• W2006075485 date "2011-10-04" @default.
• W2006075485 modified "2023-10-17" @default.
• W2006075485 title "A broad range of ophthalmologic anomalies is part of the holoprosencephaly spectrum" @default.
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• W2006075485 doi "https://doi.org/10.1002/ajmg.a.34261" @default.
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