A case of von Recklinghausen neurofibromatosis(VRNF) with oral lesion.
نویسندگان
چکیده
منابع مشابه
Retrocaval mass in patient with von Recklinghausen disease: case report.
Type I Neurofibromatosis (NF1) is an autosomal-dominant inheritable disorder, with an incidence of 1:3,000, and a prevalence of 1:4,000 to 5,000. Pathogenesis is based on mutations of the NF1 gene, a tumor suppressor gene encoding a cytoplasmic protein named neurofibromin that controls cellular proliferation. Patients affected by NF1 typically present with cutaneous neurofibromas, cafè au lait ...
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Linkage analysis of 28 genetic markers was undertaken in 108 subjects from 11 families with well-documented, classic, peripheral neurofibromatosis. Fifty-four persons were affected in one four-generation family, seven three-generation families, and three two-generation families. Lod scores were calculated using the standard LIPED programme for 49 combinations of theta male and theta female from...
متن کاملPsychological aspects of von Recklinghausen neurofibromatosis (NF1)
Neurofibromatosis is a devasting autosomal dominant disease which is extremely variable in its symptomatology, intensity, and progression. There have been numerous reports published about the physical aspects of neurofibromatosis, while psychological issues have been given little attention so far. The present article presents a review of the current knowledge concerning psychological aspects of...
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From the Division of Neurosurgery (Drs. El-Watidy, A. Jamjoom, Z. Jamjoom), King Khalid University Hospital, Riyadh and Department of Neurosurgery (Or. Selen), Northern Area Armed Forces Hospital, Hafer AI-Batin. Address reprint requests and correspondence to Or. A. Jamjoom: Consultant Neurosurgeon, Division of Neurosurgery, King Khalid University Hospital, p.a. Box 2925, Riyadh 11461, Saudi Ar...
متن کاملVon recklinghausen disease: one patient – various problems
von Recklinghausen disease (vRD), more widely known as neurofibromatosis type 1, belongs to a group of genetic disorders and it is considered to be the most common genodermatosis. The disease has an autosomal dominant pattern of inheritance that involves mutations within the NF1 gene located on chromosome 17 in locus q11.2. The product of the NF1 gene is neurofibromin and the protein is well kn...
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ژورنال
عنوان ژورنال: Japanese Journal of Oral and Maxillofacial Surgery
سال: 1988
ISSN: 2186-1579,0021-5163
DOI: 10.5794/jjoms.34.1102