Description of prosthetic treatment in case of neurofibromatosis in the course of Recklinghausen disease. Case course
Ey-Chmielewska, H.; Sobolewska, E.; Fraczak, B.ła.
Annales Academiae Medicae Stetinensis 53(2): 83-86
2007
ISSN/ISBN: 1427-440X PMID: 18557381 Document Number: 608420
Neurofibromatosis is a hereditary autosomal predominating disease occuring in one out of every 2000 or 3300 alive births. The classical form of neurofibromatosis was described by von Recklinghausen in 1882. The disease is a gene mutation, where the anomalies affect mesoderm and neuroectoderm. The paper presents the therapeutic treatment method for the case of lacking teeth restoration in a patient diagnosed with known form ofneurofibromatosis NF-1 in Recklinghausen disease.