A lesson from a reported pathogenic variant in Peutz-Jeghers syndrome: a case report
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Published on: November 11, 2014
Hu Tan1, Xianda Wei1, Pu Yang1
1The State Key Laboratory of Medical Genetics, Central South University, 110 Xiangya Road, Changsha, Hunan, 410078, China.
Insights
Peutz-Jeghers syndrome (PJS) is linked to LKB1 gene variants. This study identifies specific pathogenic LKB1 variants in Chinese PJS cases, clarifying the role of c.1062C>G.
Area of Science:
- Genetics
- Oncology
- Molecular Biology
Background:
- Peutz-Jeghers syndrome (PJS) is an autosomal dominant disorder associated with mucocutaneous hyperpigmentation, gastrointestinal polyps, and increased cancer risk.
- Pathogenic variants in the LKB1 (STK11) tumor suppressor gene are the primary cause of PJS.
Observation:
- Two sporadic Chinese PJS cases presented compound heterozygous LKB1 variants: c.890G>A/c.1062C>G and del(exon1)/c.1062C>G.
- Previous studies linked all three variants to autosomal dominant PJS.
Findings:
- This study's comprehensive data (de novo, segregation, population, in-silico, functional) indicate del(exon1) and c.890G>A are pathogenic in these PJS families.
- The variant c.1062C>G was found to be non-pathogenic in these specific PJS cases.
Implications:
- Findings aid genetic counseling for individuals with the c.1062C>G variant, regardless of PJS phenotype.
- Highlights the necessity of re-evaluating variant pathogenicity in known Mendelian disorders to prevent diagnostic errors.
Abstract:
Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant disorder characterized by mucocutaneous hyperpigmentation, gastrointestinal (GI) hamartmatous polyps, and an increased risk of various malignancies. Pathogenic variants in the LKB1 tumor suppressor gene (also known as STK11) are the major cause of PJS. In this study, compound heterozygous variants of LKB1, c.890G > A/ c.1062C > G and del(exon1)/ c.1062C > G, were identified in two sporadic Chinese PJS cases respectively. Although all these three variants had been related to the autosomal dominant PJS in previous studies, all evidences collected in this study including de novo data, segregation data, population data, in-silico data, and functional data indicated that del(exon1) and c.890G > A are pathogenic in these two PJS families rather than c.1062C > G. This finding would contribute to genetic counseling for individuals carrying the variant c.1062C > G with or without PJS phenotypes. Moreover, this finding reminds genetic counselors that it is necessary to reevaluate the pathogenicity of reported variants in a known Mendelian disorder in order to avoid a misleading decision.
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