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A novel PTCH1 mutation in a patient of nevoid basal cell carcinoma syndrome

โœ Scribed by Honma, Masaru; Ohishi, Yasushi; Uehara, Jiro; Ibe, Masaki; Kinouchi, Motoshi; Ishida-Yamamoto, Akemi; Iizuka, Hajime


Book ID
119293331
Publisher
Elsevier Science
Year
2008
Tongue
English
Weight
446 KB
Volume
50
Category
Article
ISSN
0923-1811

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โœ Maria Savino; Maria d'Apolito; Vincenza Formica; Filomena Baorda; Francesca Mari ๐Ÿ“‚ Article ๐Ÿ“… 2004 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 57 KB ๐Ÿ‘ 1 views

The nevoid basal cell carcinoma syndrome (NBCCS) is an autosomal dominant genetic disease characterized by numerous basal cell carcinomas, odontogenic keratocysts of the jaws, palmar and plantal pits, skeletal abnormalities, and calcification of the falx cerebri. The gene responsible for this syndro