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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
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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2016
2016
We report a case of healthy sixteen year old girl who presented with left eye defective vision with a Snellen best corrected… 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
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
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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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
Review
1992
Review
1992
Two cases of cardiac rhabdomyoma discovered fortuitously at foetal ultrasonography gave rise to no obstructive cardiac signs or… Expand