Nevoid basal cell carcinoma syndrome: A case report
Nevoid basal cell carcinoma syndrome (NBCCS) is an autosomal dominant inherited condition that exhibits high penetrance and variable expressivity. The syndrome is caused by mutations in patch (PTCH), a tumor suppressor gene that has been mapped to chromosome 9q22.3-q31. NBCCS is characterized by bas...
Main Authors: | , , , |
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Format: | Article |
Language: | English |
Published: |
Wolters Kluwer Medknow Publications
2018-01-01
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Series: | Journal of Dr. NTR University of Health Sciences |
Subjects: | |
Online Access: | http://www.jdrntruhs.org/article.asp?issn=2277-8632;year=2018;volume=7;issue=3;spage=200;epage=203;aulast=Dodda |