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Case Report On Neurofibromatosis Type-1: A Diagnostic Challenge | 90362
ISSN: 2161-0681

Journal of Clinical & Experimental Pathology
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Case report on neurofibromatosis type-1: A diagnostic challenge

15th Global Experts Meeting on Pathology and Laboratory Medicine

Fariha Kauser, AnshooAgarwal and Arvind Sinha

Civil Hospital Karachi, Pakistan Northern Border University, Saudi Arabia B.P. Koirala institute of Health Sciences, Nepal

Posters & Accepted Abstracts: J Clin Exp Pathol

DOI: 10.4172/2161-0681-C2-049

Abstract
Neurofibromatosis type 1 (NF1), also known as von Recklinghausen’s disease, is a human genetic disorder. It is probably the most commonly inherited disorder caused by a single gene. This is a report of five cases of Neurofibromatosis type 1. A 57 year old man affected by NF1 who has severe atrophy of the jaws and extremely unsatisfactory anatomical conditions for conventional dental restoration. Radiographic and clinical evaluations showed inadequate quantity of bone for immediate implant rehabilitation. Delayed implant protocol was performed to obtain the correct bone volume and implants were inserted in the anterior parts of both jaws to support a prosthetic restoration.
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