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dc.contributor.authorOchola, Tom J Onyango
dc.date.accessioned2013-07-11T08:37:42Z
dc.date.available2013-07-11T08:37:42Z
dc.date.issued1994
dc.identifier.citationEast African Medical Journal Vol. 7 No.11 1994 – 1994en
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/books/NBK1151/
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/47345
dc.description.abstractNevoid basal cell carcinoma syndrome (NBCCS) is characterized by the development of multiple jaw keratocysts, frequently beginning in the second decade of life, and/or basal cell carcinomas (BCCs) usually from the third decade onward. Approximately 60% of individuals have a recognizable appearance with macrocephaly, bossing of the forehead, coarse facial features, and facial milia. Most individuals have skeletal anomalies (e.g., bifid ribs, wedge-shaped vertebrae). Ectopic calcification, particularly in the falx, is present in more than 90% of affected individuals by age 20 years. Cardiac and ovarian fibromas occur in approximately 2% and 20% of individuals respectively. Approximately 5% of children with NBCCS develop medulloblastoma (primitive neuroectodermal tumor [PNET]), generally the desmoplastic subtype. Peak incidence is at age two years. Life expectancy in NBCCS is not significantly different from averageen
dc.language.isoenen
dc.publisherUniversity of Nairobien
dc.titleNevoid basal cell carcinoma syndrome:en
dc.typeArticleen
local.publisherSchool of Medicineen


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