Ey-Chmielewska H, Sobolewska E, Fraczak B
Description of prosthetic treatment in case of neurofibromatosis in the course of Recklinghausen disease. Case course. [Journal Article]
Ann Acad Med Stetin 2007; 53(2):83-6.
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.
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