Oculo-Cutaneous Manifestation of Neurofibromatosis Type 1: A Rare Case Report
Artículo
| IMSEAR
| ID: sea-202974
ABSTRACT
Introduction:
Neurofibromatosis type 1 (NF-1) is anautosomal dominant disorder involving multiple systemsand affects approximately 1 out of 3000 persons. Ocularmanifestations are very rare with lisch nodules, plexiformneurofibroma, optic pathway gliomas.Case report Here we present a case of teenager boy withneurofibromatosis type 1 presenting with Rare ocular featuresalong with systemic manifestation of the disease.Conclusion:
The proper diagnosis of NF-1 is a crucial task fora clinician due to the various clinical manifestations includingvision and life threatening malignancies in few patients, whichmay arise in the different phases of life.
Texto completo:
Disponible
Índice:
IMSEAR (Asia Sudoriental)
Año:
2020
Tipo del documento:
Artículo
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