Ocular findings and treatment of a young boy with Coats' plus

Nicolas A. Yannuzzi; Jonathan H. Tzu; Audrey C. Ko; Ditte J. Hess; Ingrid Cristian; Audina M. Berrocal

doi:10.3928/23258160-20140827-02

Ocular findings and treatment of a young boy with Coats' plus

Nicolas A. Yannuzzi, Jonathan H. Tzu, Audrey C. Ko, Ditte J. Hess, Ingrid Cristian, Audina M. Berrocal

Ophthalmology

Research output: Contribution to journal › Article › peer-review

3 Scopus citations

Abstract

The authors describe a 34-month-old boy who presented with a bilateral and asymmetric exudative retinopathy with similarities to Coats' disease. The patient's medical history was remarkable for hypotonia, developmental delay, seizures, and intracranial calcifications. Genetic testing revealed a diagnosis of Coats' plus. This rare genetic disease should be in the differential diagnosis in patients who present with a bilateral and asymmetric Coats'-like retinopathy in the presence of other systemic abnormalities.

Original language	English (US)
Pages (from-to)	462-465
Number of pages	4
Journal	Ophthalmic Surgery Lasers and Imaging Retina
Volume	45
Issue number	5
DOIs	https://doi.org/10.3928/23258160-20140827-02
State	Published - Sep 1 2014

ASJC Scopus subject areas

Surgery
Ophthalmology

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abstract = "The authors describe a 34-month-old boy who presented with a bilateral and asymmetric exudative retinopathy with similarities to Coats' disease. The patient's medical history was remarkable for hypotonia, developmental delay, seizures, and intracranial calcifications. Genetic testing revealed a diagnosis of Coats' plus. This rare genetic disease should be in the differential diagnosis in patients who present with a bilateral and asymmetric Coats'-like retinopathy in the presence of other systemic abnormalities.",

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AU - Tzu, Jonathan H.

AU - Ko, Audrey C.

AU - Hess, Ditte J.

AU - Cristian, Ingrid

AU - Berrocal, Audina M.

PY - 2014/9/1

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AB - The authors describe a 34-month-old boy who presented with a bilateral and asymmetric exudative retinopathy with similarities to Coats' disease. The patient's medical history was remarkable for hypotonia, developmental delay, seizures, and intracranial calcifications. Genetic testing revealed a diagnosis of Coats' plus. This rare genetic disease should be in the differential diagnosis in patients who present with a bilateral and asymmetric Coats'-like retinopathy in the presence of other systemic abnormalities.

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Ocular findings and treatment of a young boy with Coats' plus

Abstract

ASJC Scopus subject areas

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