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Updated: Jan 10, 2026

Cell Population Analyses During Skin Carcinogenesis
Published on: August 21, 2013
Nevoid Basal Cell Carcinoma Syndrome: Three Cases from the Same Family
Ying Yan1, Huajie Zhong1, Xue Xu1
1From the Department of Dermatology, Huzhou Central Hospital, Fifth School of Clinical Medicine of Zhejiang Chinese Medical University, Affiliated Central Hospital of Huzhou University, Huzhou, Zhejiang, China.
Nevoid basal cell carcinoma syndrome (NBCCS) is a rare genetic disorder. This study details a family with NBCCS, highlighting PTCH gene mutations and characteristic symptoms for early diagnosis and management.
Area of Science:
- Genetics
- Dermatology
- Oncology
Background:
- Nevoid basal cell carcinoma syndrome (NBCCS) is a rare autosomal dominant disorder.
- It is primarily caused by mutations in the PTCH gene.
- While sporadic cases are documented, detailed family pedigrees are infrequently reported.
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