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Germline mutation analysis in the CYLD gene in Chinese patients with multiple trichoepitheliomas.
- Source :
-
Genetics and molecular research : GMR [Genet Mol Res] 2014 Nov 14; Vol. 13 (4), pp. 9650-5. Date of Electronic Publication: 2014 Nov 14. - Publication Year :
- 2014
-
Abstract
- Trichoepithelioma is a benign neoplasm that primarily shows follicular germinative differentiation. Classic trichoepithelioma typically presents as a skin-colored papule or nodule on the face or upper trunk; lesions have a predilection for the nose. Trichoepithelioma can be sporadic or familial and solitary or multiple. Most previously reported multiple trichoepithelioma cases are familial, and germline CYLD mutations could be detected in some patients. We performed mutational analysis of the germline CYLD gene in 8 Chinese multiple trichoepitheliomas patients, 6 of which were sporadic cases. A heterozygous missense mutation (c.1112C>A) in the 9th exon of the CYLD gene was detected in some mother-daughter patients. However, the germline CYLD mutation could not be detected in the 6 non-familial cases. The results suggest that the pathogenesis of sporadic multiple trichoepitheliomas may differ from that of familial cases. Our findings also further confirmed the genetic heterogeneity of multiple trichoepitheliomas.
- Subjects :
- Adolescent
Adult
Asian People
Child
DNA Mutational Analysis
Deubiquitinating Enzyme CYLD
Exons
Female
Heterozygote
Humans
Inheritance Patterns
Male
Middle Aged
Neoplastic Syndromes, Hereditary ethnology
Neoplastic Syndromes, Hereditary pathology
Skin metabolism
Skin pathology
Skin Neoplasms
Germ-Line Mutation
Mutation, Missense
Neoplastic Syndromes, Hereditary diagnosis
Neoplastic Syndromes, Hereditary genetics
Tumor Suppressor Proteins genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1676-5680
- Volume :
- 13
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Genetics and molecular research : GMR
- Publication Type :
- Academic Journal
- Accession number :
- 25501176
- Full Text :
- https://doi.org/10.4238/2014.November.14.10