Article
Neurofibromatosis Type 1 With Cherubism-like Phenotype, Multiple Osteolytic Bone Lesions of Lower Extremities, and Alagille-syndrome: Case Report With Literature Survey.
In vivo (Athens, Greece) - 1 Jan 2000
Friedrich Reinhard E, Zustin Jozef, Luebke Andreas M, Rosenbaum Thorsten, Gosau Martin, Hagel Christian, Kohlrusch Felix K, Wieland Ilse, Zenker Martin
Abstract excerpt
BACKGROUND/AIM: Neurofibromatosis type 1 (NF) is an autosomal dominant hereditary disease. The cardinal clinical findings include characteristic skeletal alterations. Difficulties in diagnosis and therapy can arise if an individual has further illnesses. CASE REPORT: This is a case report of a 16-year-old patient affected by NF1. She also suffered from Alagille syndrome and the consequences of fetal alcohol...
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