Neurofibromatosis

An autosomal dominant hereditary neoplastic syndrome. Two distinct clinicopathological entities are recognized: neurofibromatosis type 1 and neurofibromatosis type 2. Neurofibromatosis type 1 is associated with the presence of cafe-au-lait cutaneous lesions, multiple neurofibromas, malignant peripheral nerve sheath tumors, optic nerve gliomas, and bone lesions. Neurofibromatosis type 2 is associated with the presence of schwannomas, meningiomas, and gliomas.

Disease Alternative Name

neurofibromatosis syndrome

nos

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Dr. Gowhar Ahmad

HESDING DEPT OF PAEDIATRIC OPHTHALMOLOGY OCULOPLATY NEURO OPHTHALMOLOGY

SOME OF CAUSES IF ANGIOD STREAKS 1 P X E 2 PAGETS DESEASE 3 EVDVS 4 ACROMEGALY 5 OLD AFE 6 LEAD POISONING 7 HYPERPHOSPHOTEAMIA 8 S C DESEASE 10 D M 11 HIGH MYOPIA 12 S W SYNDROME 13 NEURIFIBRAMATOSIS ⁷ 14 SPHEROCYTOSIS 15 HEAMOCHROCYTOSIS

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Dr. Gowhar Ahmad

HESDING DEPT OF PAEDIATRIC OPHTHALMOLOGY OCULOPLATY NEURO OPHTHALMOLOGY

Maintenance of NEURIFIBRAMATOSIS LIDS FEEL LIKE BAG OF WORMS PTOSIS PROPTOSIS UNILATERAL GLAUCOMA CONJUCTIVAL INVOLMENT ENLARGED CORNEAL NERVES IRIS CHANGES PIGMENTORY AND NAVIID CHANGES GENERALISED NODULES OF IRIS LEISH NODULES PARTIAL COL...See More

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