Type 1 Neurofibromatosis Sans Neurofibroma: A Case Report Emphasizing the Role of Ocular Examination
Neurofibromatosis type 1 (NF1) is one of the most common genetic disorders and is inherited in an autosomal dominant fashion. NF1 is a member of the RASopathies, a class of congenital disorders brought on by mutations in the Ras/mitogen-activated protein kinase pathway. Dermatologic manifestations a...
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| Main Authors: | , |
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| Format: | Book |
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Wolters Kluwer Medknow Publications,
2024-09-01T00:00:00Z.
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| Call Number: |
A1234.567 |
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| Copy 1 | Available |