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Retinal hamartoma

A hamartoma (a benign, focal malformation consisting of a disorganized mixture of cells and tissues) of the retina. [HPO:probinson]
National Institutes of Health

Papers overview

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Review
2018
Review
2018
BACKGROUND Neurofibromatosis type 2 (NF2) is a genetic condition with an autosomal dominant pattern of inheritance and incomplete… Expand
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2018
2018
INTRODUCTION Tuberous sclerosis is a rare multisystemic disease with an autosomal dominant inheritance pattern. There are few… Expand
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2016
2016
BACKGROUND A sensitive method is required to detect retinal hamartomas in patients with tuberous sclerosis complex (TSC). The aim… Expand
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2009
2009
PURPOSE Focal cortical dysplasia (FCD) is a common cause of pharmacoresistant human epilepsy. FCD has frequently been discussed… Expand
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2009
2009
BACKGROUND Neurofibromatosis type 2 (NF2) has long been regarded as an adult onset disease. However, it is now known that many… Expand
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2008
2008
Tuberous sclerosis is a genetic disease with autosomal dominant inheritance, associated with hamartomata in several organs and… Expand
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2007
2007
A 29-year-old lady with a bad obstetric history and portal vein thrombosis, presented to the Skin OPD for facial lesions. On… Expand
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Review
2007
Review
2007
BACKGROUND Retinal hamartoma is a common finding in tuberous sclerosis, but the symptomatic changes of this lesion have rarely… Expand
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2000
2000
We report the clinical and angiographic features as well as the natural course of an optic disk and juxtapapillary combined… Expand
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1998
1998
Editor,—The electroretinogram (ERG) and visual evoked potential (VEP) to pattern reversal stimulation became degraded in… Expand
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