Add to ORKGRetinal tumor in NF-2 referred to as a CPERH (choroidal pigment epithelial retinal hamartoma). Patient, a 16 year old girl, had bilateral acoustic neurinomas. Pair with R1_F2b. Same eye.Optic disc; RetinaRetinal hamartoma; Bilateral acoustic neurinomaSuperior temporal field defectVBneurofibromatosistw
To the best of our knowledge this is the first description of a choroidal melanoma with documented g...
6 year old with neurofibromatosis (NF1). Right eye went blind. Light perception. Optic canal enlarge...
VBneurofibromatosisPresenting Symptom: Loss of vision OD. Pathology: Glioma. Clnical: Gliomas of the...
Retinal tumor in NF-2 referred to as a CPERH (choroidal pigment epithelial retinal hamartoma). Patie...
We describe a young patient with combined hamartoma of the retina and retinal pigment epithelium who...
A 15-year-old male patient with a known history of neurofibromatosis Type 2 (NF-2) presented to a te...
Neurofibromatosis is the most common phakomatosis, with an estimated prevalence of approximately one...
This 22-year-old woman has neurofibromatosis, type 2. Acuity, color plates, pupillary responses, sli...
Neurofibromatosis 2 is a rare autosomal dominant neurocutaneous disorder classically characterized b...
Neurofibromatosis has been recently acknowledged as consisting of a number of different diseases. Ne...
A 13 year old Afghani boy was referred with an apparent isolated optic nerve sheath meningioma. The ...
Neurofibromatosis type 2 (NF2) is a rare genetic disorder, affecting the central nervous system and ...
Abstract Neurofibromatosis type 2 (NF2) is a rare genetic disease involving multiple tumors of the c...
Neurofibromatosis type 2 usually presents with bilateral acoustic schwannomas. We highlight the rare...
<p>Magnetic resonance (MR) imaging performed in a 47-year old patient with neurofibromatosis type 2 ...
To the best of our knowledge this is the first description of a choroidal melanoma with documented g...
6 year old with neurofibromatosis (NF1). Right eye went blind. Light perception. Optic canal enlarge...
VBneurofibromatosisPresenting Symptom: Loss of vision OD. Pathology: Glioma. Clnical: Gliomas of the...
Retinal tumor in NF-2 referred to as a CPERH (choroidal pigment epithelial retinal hamartoma). Patie...
We describe a young patient with combined hamartoma of the retina and retinal pigment epithelium who...
A 15-year-old male patient with a known history of neurofibromatosis Type 2 (NF-2) presented to a te...
Neurofibromatosis is the most common phakomatosis, with an estimated prevalence of approximately one...
This 22-year-old woman has neurofibromatosis, type 2. Acuity, color plates, pupillary responses, sli...
Neurofibromatosis 2 is a rare autosomal dominant neurocutaneous disorder classically characterized b...
Neurofibromatosis has been recently acknowledged as consisting of a number of different diseases. Ne...
A 13 year old Afghani boy was referred with an apparent isolated optic nerve sheath meningioma. The ...
Neurofibromatosis type 2 (NF2) is a rare genetic disorder, affecting the central nervous system and ...
Abstract Neurofibromatosis type 2 (NF2) is a rare genetic disease involving multiple tumors of the c...
Neurofibromatosis type 2 usually presents with bilateral acoustic schwannomas. We highlight the rare...
<p>Magnetic resonance (MR) imaging performed in a 47-year old patient with neurofibromatosis type 2 ...
To the best of our knowledge this is the first description of a choroidal melanoma with documented g...
6 year old with neurofibromatosis (NF1). Right eye went blind. Light perception. Optic canal enlarge...
VBneurofibromatosisPresenting Symptom: Loss of vision OD. Pathology: Glioma. Clnical: Gliomas of the...