| Literature DB >> 23479190 |
Katsunori Fujii1, Hirofumi Ohashi, Maiko Suzuki, Hiromi Hatsuse, Tadashi Shiohama, Hideki Uchikawa, Toshiyuki Miyashita.
Abstract
Nevoid basal cell carcinoma syndrome (NBCCS) is an autosomal dominant disorder characterized by developmental defects and tumorigenesis. The gene responsible for NBCCS is PTCH1, encoding a receptor for the secreted protein, sonic hedgehog. Recently, a Chinese family with NBCCS carrying a missense mutation in PTCH2, a close homolog of PTCH1, was reported. However, the pathological significance of missense mutations should be discussed cautiously. Here, we report a 13-year-old girl diagnosed with NBCCS based on multiple keratocystic odontogenic tumors and rib anomalies carrying a frameshift mutation in the PTCH2 gene (c.1172_1173delCT). Considering the deleterious nature of the frameshift mutation, our study further confirmed a causative role for the PTCH2 mutation in NBCCS. The absence of typical phenotypes in this case such as palmar/plantar pits, macrocephaly, falx calcification, hypertelorism and coarse face, together with previously reported cases, suggested that individuals with NBCCS carrying a PTCH2 mutation may have a milder phenotype than those with a PTCH1 mutation.Entities:
Mesh:
Substances:
Year: 2013 PMID: 23479190 DOI: 10.1007/s10689-013-9623-1
Source DB: PubMed Journal: Fam Cancer ISSN: 1389-9600 Impact factor: 2.375