Add to ORKGDiagnostic criteria Neurofibromatosis 1 least two of the seven: Six or more café-au-lait macules over 5 mm in greatest diameter in pre-pubertal individuals and over 15 mm in greatest diameter in post-pubertal individuals, (2) Two or more neurofibromas of any type or one plexiform neurofibroma, (3) Freckling in the axillary or inguinal regions, (4) Optic glioma, (5) Two or more Lisch nodules, (6) Any distinctive osseous lesion such as sphenoid dysplasia or thinning of the long bone cortex with or without pseudarthrosis. (7) A first degree relative with NF-1. RESULTS HISTORY: A 4 day Female baby was presented by its mother with bilateral cloudy cornea's, enlarged eye balls noticed by parents. Multiple lesions on face and whole body, enl...
Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction...
VBneurofibromatosisPresenting Symptom: Loss of vision OD. Pathology: Glioma. Clnical: Gliomas of the...
Neurofibromatosis type 1 (NF1) or Von Recklinghausen's disease is a dominantly inherited genetic, mu...
Neurofibromatosis, type 1, is an autosomal dominant phakomatosis characterized by Lisch nodules of t...
Ocular type 1 neurofibromatosis is an autosomal dominant phacomatosis with variable expression and t...
Neurofibromatosis type 1 (NF1) is a rare genetic disorder with an autosomal dominant transmission an...
BACKGROUND: Neurofibromatosis type 1 (NF-1) is an autsomal dominant disorder which can occasionally...
We report the case of a 29-year-old female patient who presented with an acute onset of anisocoria, ...
11 individuals were diagnosed to have neurofibromatosis type 1 and were examined for evidence of any...
Introduction: Neurofibromatosis Type 1 (NF-1) is a genetic disorder that occurs in 1:2500–3000 live ...
Neurofibromatosis (NF) is a term that has been applied to a variety of related syndromes, characteri...
Neurofibromatosis type 1 (NF1) is an inherited systemic disease with frequent ocular involvement. A ...
Neurofibromatosis has been recently acknowledged as consisting of a number of different diseases. Ne...
Neurofibromatosis type 1 (NF1) is a neurocutaneous condition with an autosomal dominant pattern of i...
INTRODUCTION: Neurofibromatosis Type 1 (NF1) or Von Recklinghausen’s disease, is a rare genetic di...
Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction...
VBneurofibromatosisPresenting Symptom: Loss of vision OD. Pathology: Glioma. Clnical: Gliomas of the...
Neurofibromatosis type 1 (NF1) or Von Recklinghausen's disease is a dominantly inherited genetic, mu...
Neurofibromatosis, type 1, is an autosomal dominant phakomatosis characterized by Lisch nodules of t...
Ocular type 1 neurofibromatosis is an autosomal dominant phacomatosis with variable expression and t...
Neurofibromatosis type 1 (NF1) is a rare genetic disorder with an autosomal dominant transmission an...
BACKGROUND: Neurofibromatosis type 1 (NF-1) is an autsomal dominant disorder which can occasionally...
We report the case of a 29-year-old female patient who presented with an acute onset of anisocoria, ...
11 individuals were diagnosed to have neurofibromatosis type 1 and were examined for evidence of any...
Introduction: Neurofibromatosis Type 1 (NF-1) is a genetic disorder that occurs in 1:2500–3000 live ...
Neurofibromatosis (NF) is a term that has been applied to a variety of related syndromes, characteri...
Neurofibromatosis type 1 (NF1) is an inherited systemic disease with frequent ocular involvement. A ...
Neurofibromatosis has been recently acknowledged as consisting of a number of different diseases. Ne...
Neurofibromatosis type 1 (NF1) is a neurocutaneous condition with an autosomal dominant pattern of i...
INTRODUCTION: Neurofibromatosis Type 1 (NF1) or Von Recklinghausen’s disease, is a rare genetic di...
Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction...
VBneurofibromatosisPresenting Symptom: Loss of vision OD. Pathology: Glioma. Clnical: Gliomas of the...
Neurofibromatosis type 1 (NF1) or Von Recklinghausen's disease is a dominantly inherited genetic, mu...