Macular coloboma and skeletal abnormality.

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Macular coloboma and skeletal abnormality.

Of the other members of the family only the patients' mother was examined clinically by us and no abnormality was found. She gave a clear account of the large family on her own and her husband's side and mentioned only one individual with an abnormality: this was the blind child of a paternal aunt of the propositi who married a full cousin. However, the findings of his ophthalmologist (corneal ...

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[Atypical macular coloboma: a case report].

CLINICAL CASE This was a 15-month-old boy who had macular retinochoroidal lesions in both eyes following maternal varicella during pregnancy. DISCUSSION The scars were suggestive of congenital chorioretinal infection, but because of negative serology and the clinical picture, we believe the problems are atypical macular colobomata.

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Bilateral macular coloboma and pigmented paravenous retinochoroidal atrophy.

A patient had bilateral macular coloboma with aggregations of pigment clumps located perivascularly, predominantly paravenously, and in other parts of the retina. The Toxoplasma IgG antibody was negative. The diagnosis of bilateral macular coloboma with pigmented paravenous retinochoroidal atrophy was made and seemed to be a developmental abnormality in origin.

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Pediatric Choroidal Coloboma with Macular Hole at the Edge of the Coloboma.

Originally received: July 13, 2016. Final revision: December 23, 2016. Accepted: January 5, 2017. Available online: February 14, 2017. Manuscript no. 2016-1470. 1 Sacrocuore Hospital, Verona, Italy. 2 Department of Computer Science, University of Verona, Verona, Italy. 3 Department of Ophthalmology, Sant’Anna Institute, Brescia, Italy. Financial Disclosure(s): The authors have no proprietary or...

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ژورنال

عنوان ژورنال: British Journal of Ophthalmology

سال: 1969

ISSN: 0007-1161

DOI: 10.1136/bjo.53.5.346