Add to ORKGWe describe a young patient with combined hamartoma of the retina and retinal pigment epithelium who developed bilateral acoustic neuromas and meningiomas of the cervical-medullary junction and fifth cranial nerve. This case illustrates the association between combined hamartoma of the retina and retinal pigment epithelium and neurofibromatosis type 2. The authors recommend that children with a combined hamartoma of the retina and retinal pigment epithelium be screened for neurofibromatosis type 2
Combined hamartoma of the retina and of the retinal pigment epithelium are extremely rare benign...
Neurofibromatosis type 2 usually presents with bilateral acoustic schwannomas. We highlight the rare...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
A 15-year-old male patient with a known history of neurofibromatosis Type 2 (NF-2) presented to a te...
Retinal tumor in NF-2 referred to as a CPERH (choroidal pigment epithelial retinal hamartoma). Patie...
Neurofibromatosis is the most common phakomatosis, with an estimated prevalence of approximately one...
AbstractWe report a family of three siblings followed between 2005 and 2011 with bilateral combined ...
Neurofibromatosis has been recently acknowledged as consisting of a number of different diseases. Ne...
We report the case of a 38-year-old male patient with a 1-year history of progressively blurred visi...
Neurofibromatosis 2 is a rare autosomal dominant neurocutaneous disorder classically characterized b...
We report the case of a 56-year-old woman who presented for a routine ophthalmological examination w...
This 22-year-old woman has neurofibromatosis, type 2. Acuity, color plates, pupillary responses, sli...
Purpose: Combined hamartoma of the retina and retinal pigment epithelium is a rare benign tumor char...
Abstract Neurofibromatosis type 2 (NF2) is a rare genetic disease involving multiple tumors of the c...
Combined hamartoma of the retina and retinal pigment epithelium (RPE) is a rare, benign, congenital ...
Combined hamartoma of the retina and of the retinal pigment epithelium are extremely rare benign...
Neurofibromatosis type 2 usually presents with bilateral acoustic schwannomas. We highlight the rare...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
A 15-year-old male patient with a known history of neurofibromatosis Type 2 (NF-2) presented to a te...
Retinal tumor in NF-2 referred to as a CPERH (choroidal pigment epithelial retinal hamartoma). Patie...
Neurofibromatosis is the most common phakomatosis, with an estimated prevalence of approximately one...
AbstractWe report a family of three siblings followed between 2005 and 2011 with bilateral combined ...
Neurofibromatosis has been recently acknowledged as consisting of a number of different diseases. Ne...
We report the case of a 38-year-old male patient with a 1-year history of progressively blurred visi...
Neurofibromatosis 2 is a rare autosomal dominant neurocutaneous disorder classically characterized b...
We report the case of a 56-year-old woman who presented for a routine ophthalmological examination w...
This 22-year-old woman has neurofibromatosis, type 2. Acuity, color plates, pupillary responses, sli...
Purpose: Combined hamartoma of the retina and retinal pigment epithelium is a rare benign tumor char...
Abstract Neurofibromatosis type 2 (NF2) is a rare genetic disease involving multiple tumors of the c...
Combined hamartoma of the retina and retinal pigment epithelium (RPE) is a rare, benign, congenital ...
Combined hamartoma of the retina and of the retinal pigment epithelium are extremely rare benign...
Neurofibromatosis type 2 usually presents with bilateral acoustic schwannomas. We highlight the rare...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...