Bilateral congenital mydriasis in a child case
نویسندگان
چکیده
منابع مشابه
Bilateral congenital mydriasis in a child case.
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...
متن کاملBilateral 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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Objectives: Microtia is the most commonly seen congenital ear defect, and involves an auricular deformity either unilaterally or bilaterally. The aim of this study was to fabricate silicone prostheses for a child with bilateral microtia using an innovative technique. Methods: This method involved the construction of bilateral ear prostheses using clips, which were located within the layers o...
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objectives: microtia is the most commonly seen congenital ear defect, and involves an auricular deformity either unilaterally or bilaterally. the aim of this study was to fabricate silicone prostheses for a child with bilateral microtia using an innovative technique. methods: this method involved the construction of bilateral ear prostheses using clips, which were located within the layers of t...
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ژورنال
عنوان ژورنال: Türk Pediatri Arşivi
سال: 2016
ISSN: 1306-0015,1308-6278
DOI: 10.5152/turkpediatriars.2016.4194