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1 Scheme of occurs genomic region of Neurofibromatosis type 1 (NF1) Mutation (Wimmer et al. 2002).

1 Scheme of occurs genomic region of Neurofibromatosis type 1 (NF1) Mutation (Wimmer et al. 2002).

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Figure 1.1 Scheme of occurs genomic region of Neurofibromatosis type 1...
Figure 1.2 Cutaneous neurofibroma at the upper eyelid (Cannon et al. 2018).
Figure 1.3 Malignant peripheral nerve sheath tumor develops at limb...
Figure 4: Ophthalmic and adnexal manifestations affect the upper...
Figure 5: Tinning of the bones due to skeletal alterations (Karolak,...
A Review: Symptoms, Gene Analysis, Diagnosis and Treatment of Neurofibromatosis type 1 (NF1) syndrome
Article
Full-text available
  • Oct 2019
Abstract Neurofibromatosis type 1 (NF1) is an autosomal predominant, mucocutaneous and inclination disorder. They include it in the development of benign and malignant tumors. Hereditary change in NF1 prompts changes in the outflow of cytoplasmic protein. 90% of all cases represent NF1 in neurofibromatosis. children tainted with NF1, they distingui...
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Neurofibromatosis type 1 (NF1) and type 2 (NF2) are autosomal dominant diseases. Patients with NF1 or NF2 have the potential to develop benign and malignant tumors. We present a 17-year-old patient with undiagnosed NF1-related multiple plexiform neurofibromas (PNs). The patient was admitted to our department for his left limb paresthesia. He had ca...
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