Gillespie syndrome reported as bilateral congenital mydriasis.
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چکیده
منابع مشابه
Bilateral congenital mydriasis.
A 73-year-old white woman with bilateral congenital mydriasis had no other obvious abnormalities. The pupils reacted almost imperceptibly to light. There was no detectable reaction to accommodation and convergence. Pupillary response to pilocarpine 4% solution indicated the presence of the sphincter muscle. However, the failure of the pupil to react to a potent cholinesterase inhibitor (demecar...
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Congenital mydriasis is defined as congenital absence of iris sphincter muscle which occurs rarely and shows autosomal dominant inheritance (1-4). It was described by White and Fulton (2) in 1937 for the first time. Fixed and dilated pupil is present from the time of birth, observed more frequently in girls and typically bilateral (1-4). Iris sphincter traumas, pharmacological dilatation and ac...
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Septo-optic dysplasia (SOD)[MIM182230] consisting of a heterogeneous and uncommon condition characterised by the classictriad: optic nerve hypoplasia, abnormalities of pituitary hormone, and defects of thebrain midline (including agenesis of the septum pellucidum and/or the corpus callosum; ithas also been described associated cortical malformations, it was referred to as SOD plus syndrome).We ...
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CC This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons. org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. Author contributions: BDC: conception and design, acquisition of data, analysis and inte...
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ژورنال
عنوان ژورنال: British Journal of Ophthalmology
سال: 1993
ISSN: 0007-1161
DOI: 10.1136/bjo.77.12.827-c