Copy number variants and rasopathies: germline KRAS duplication in a patient with syndrome including pigmentation abnormalities
- PMID: 27450488
- PMCID: PMC4957908
- DOI: 10.1186/s13023-016-0479-y
Copy number variants and rasopathies: germline KRAS duplication in a patient with syndrome including pigmentation abnormalities
Abstract
RAS/MAPK pathway germline mutations were described in Rasopathies, a class of rare genetic syndromes combining facial abnormalities, heart defects, short stature, skin and genital abnormalities, and mental retardation. The majority of the mutations identified in the Rasopathies are point mutations which increase RAS/MAPK pathway signaling. Duplications encompassing RAS/MAPK pathway genes (PTPN11, RAF1, MEK2, or SHOC2) were more rarely described. Here we report, a syndromic familial case of a 12p duplication encompassing the dosage sensitive gene KRAS, whose phenotype overlapped with rasopathies. The patient was referred because of a history of mild learning disabilities, small size, facial dysmorphy, and pigmentation abnormalities (café-au-lait and achromic spots, and axillar lentigines). This phenotype was reminiscent of rasopathies. No mutation was identified in the most common genes associated with Noonan, cardio-facio-cutaneous, Legius, and Costello syndromes, as well as neurofibromatosis type 1. The patient constitutional DNA exhibited a ~10.5 Mb duplication at 12p, including the KRAS gene. The index case's mother carried the same chromosome abnormality and also showed development delay with short stature, and numerous café-au-lait spots. Duplication of the KRAS gene may participate in the propositus phenotype, in particular of the specific pigmentation abnormalities. Array-CGH or some other assessment of gene/exon CNVs of RAS/MAPK pathway genes should be considered in the evaluation of individuals with rasopathies.
Keywords: 12p duplication; CNV; Café-au-lait spots; KRAS; Rasopathies.
Figures

Similar articles
-
Clinical features and molecular genetics of patients with RASopathies: expanding the phenotype with rare genes and novel variants.Eur J Pediatr. 2024 Dec 27;184(1):108. doi: 10.1007/s00431-024-05825-8. Eur J Pediatr. 2024. PMID: 39725732
-
Multiple café au lait spots in familial patients with MAP2K2 mutation.Am J Med Genet A. 2014 Feb;164A(2):392-6. doi: 10.1002/ajmg.a.36288. Epub 2013 Dec 5. Am J Med Genet A. 2014. PMID: 24311457 Review.
-
Craniosynostosis in patients with RASopathies: Accumulating clinical evidence for expanding the phenotype.Am J Med Genet A. 2017 Sep;173(9):2346-2352. doi: 10.1002/ajmg.a.38337. Epub 2017 Jun 26. Am J Med Genet A. 2017. PMID: 28650561
-
Noonan, Costello and cardio-facio-cutaneous syndromes: dysregulation of the Ras-MAPK pathway.Expert Rev Mol Med. 2008 Dec 9;10:e37. doi: 10.1017/S1462399408000902. Expert Rev Mol Med. 2008. PMID: 19063751 Review.
-
Rasopathies case report: concurrence of two pathogenic variations de novo in NF1 and KRAS genes in a patient.BMC Pediatr. 2019 Apr 5;19(1):92. doi: 10.1186/s12887-019-1463-1. BMC Pediatr. 2019. PMID: 30953504 Free PMC article.
Cited by
-
The RASopathies: from pathogenetics to therapeutics.Dis Model Mech. 2022 Feb 1;15(2):dmm049107. doi: 10.1242/dmm.049107. Epub 2022 Feb 18. Dis Model Mech. 2022. PMID: 35178568 Free PMC article. Review.
-
RAS GTPase-dependent pathways in developmental diseases: old guys, new lads, and current challenges.Curr Opin Cell Biol. 2018 Dec;55:42-51. doi: 10.1016/j.ceb.2018.06.007. Epub 2018 Jul 11. Curr Opin Cell Biol. 2018. PMID: 30007125 Free PMC article. Review.
-
Pigmentary mosaicism as a recurrent clinical manifestation in three new patients with mosaic trisomy 12 diagnosed postnatally: cases report and literature review.BMC Med Genomics. 2022 Oct 31;15(1):224. doi: 10.1186/s12920-022-01382-x. BMC Med Genomics. 2022. PMID: 36316743 Free PMC article. Review.
-
Repeating or spacing learning sessions are strategies for memory improvement with shared molecular and neuronal components.Neurobiol Learn Mem. 2020 Jul;172:107233. doi: 10.1016/j.nlm.2020.107233. Epub 2020 May 1. Neurobiol Learn Mem. 2020. PMID: 32360730 Free PMC article.
-
Examining Demographic and Clinical Traits in Neurofibromatosis Type 1 Patients: Insights into Vitamin D Levels and Connections with Nevus Anemicus and Neurofibromas.Indian J Dermatol. 2025 Jan-Feb;70(1):11-17. doi: 10.4103/ijd.ijd_141_24. Epub 2024 Dec 30. Indian J Dermatol. 2025. PMID: 39896307 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials
Miscellaneous