Phenotype-genotype analysis of 242 individuals with RASopathies: 18-year experience of a tertiary center in Brazil

Carregando...
Imagem de Miniatura
Citações na Scopus
13
Tipo de produção
article
Data de publicação
2020
Título da Revista
ISSN da Revista
Título do Volume
Editora
WILEY
Citação
AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS, v.184, n.4, Special Issue, p.896-911, 2020
Projetos de Pesquisa
Unidades Organizacionais
Fascículo
Resumo
We report the clinical and molecular data of a large cohort comprising 242 individuals with RASopathies, from a single Tertiary Center in Brazil, the largest study from Latin America. Noonan syndrome represented 76% of the subjects, with heterozygous variants in nine different genes, mainly PTPN11, SOS1, RAF1, LZTR1, and RIT1, detected by Sanger and next-generation sequencing. The latter was applied to 126 individuals, with a positive yield of 63% in genes of the RAS/MAPK cascade. We present evidence that there are some allelic differences in PTPN11 across distinct populations. We highlight the clinical aspects that pose more medical concerns, such as the cardiac anomalies, bleeding diathesis and proliferative lesions. The genotype-phenotype analysis between the RASopathies showed statistically significant differences in some cardinal features, such as craniofacial and cardiac anomalies, the latter also statistically significant for different genes in Noonan syndrome. We present two individuals with a Noonan syndrome phenotype, one with an atypical, structural cardiac defect, harboring variants in genes mainly associated with isolated hypertrophic cardiomyopathy and discuss the role of these variants in their phenotype.
Palavras-chave
genotype&#8211, phenotype correlation, next&#8208, generation sequencing, Noonan syndrome, RAS, MAPK pathway, RASopathies
Referências
  1. Altmuller F, 2017, EUR J HUM GENET, V25, P823, DOI 10.1038/ejhg.2017.65
  2. Aoki Y, 2016, J HUM GENET, V61, P33, DOI 10.1038/jhg.2015.114
  3. Augiere C, 2015, PLOS ONE, V10, DOI 10.1371/journal.pone.0127903
  4. Bertola DR, 2012, CLIN GENET, V81, P595, DOI 10.1111/j.1399-0004.2011.01764.x
  5. Bertola D, 2017, AM J MED GENET A, V173, P1309, DOI 10.1002/ajmg.a.38178
  6. Bertola D, 2017, AM J MED GENET A, V173, P824, DOI 10.1002/ajmg.a.38070
  7. Bertola DR, 2006, GENET TEST, V10, P186, DOI 10.1089/gte.2006.10.186
  8. Bertola DR, 2014, AM J MED GENET A, V164, P2952, DOI 10.1002/ajmg.a.36722
  9. Bertola DR, 2007, J HUM GENET, V52, P521, DOI 10.1007/s10038-007-0146-1
  10. Bertola DR, 2005, AM J MED GENET A, V136A, P242, DOI 10.1002/ajmg.a.30813
  11. Bhoj EJ, 2017, GENET MED, V19, P715, DOI 10.1038/gim.2016.169
  12. Brasil AS, 2012, AM J MED GENET A, V158A, P1178, DOI 10.1002/ajmg.a.35270
  13. Brasil AS, 2010, ARQ BRAS ENDOCRINOL, V54, P717, DOI 10.1590/S0004-27302010000800009
  14. Brasil AS, 2010, GENET TEST MOL BIOMA, V14, P425, DOI 10.1089/gtmb.2009.0192
  15. Calcagni G, 2018, HEART FAIL CLIN, V14, P225, DOI 10.1016/j.hfc.2017.12.005
  16. Carapito R, 2014, J HUM GENET, V59, P57, DOI 10.1038/jhg.2013.118
  17. Chen H, 2019, ORPHANET J RARE DIS, V14, DOI 10.1186/s13023-019-1010-z
  18. Chinton J, 2020, AM J MED GENET A, V182, P409, DOI 10.1002/ajmg.a.61445
  19. Chinton J, 2019, ARCH ARGENT PEDIATR, V117, P330, DOI 10.5546/aap.2019.eng.330
  20. Quaio CRDC, 2013, CLINICS, V68, P1079, DOI 10.6061/clinics/2013(08)03
  21. da Silva FM, 2016, AM J MED GENET A, V170, P1525, DOI 10.1002/ajmg.a.37639
  22. Digilio MC, 2006, AM J MED GENET A, V140A, P740, DOI 10.1002/ajmg.a.31156
  23. Eyselbergs M, 2014, JBR-BTR, V97, P90, DOI 10.5334/jbr-btr.20
  24. Ferrari L, 2020, EUR J HUM GENET, V28, P1432, DOI 10.1038/s41431-020-0658-0
  25. Gelb BD, 2015, PROG PEDIATR CARDIOL, V39, P13, DOI 10.1016/j.ppedcard.2015.01.002
  26. Holzmann J, 2018, CARDIOL YOUNG, V28, P647, DOI 10.1017/S1047951117002827
  27. Ilkovski B, 2005, NEUROMUSCULAR DISORD, V15, P829, DOI 10.1016/j.nmd.2005.08.004
  28. Johnston JJ, 2018, GENET MED, V20, P1175, DOI 10.1038/gim.2017.249
  29. Karbach J, 2012, AM J MED GENET A, V158A, P2283, DOI 10.1002/ajmg.a.35493
  30. Kehrer-Sawatzki H, 2017, HUM GENET, V136, P349, DOI 10.1007/s00439-017-1766-y
  31. Koh AL, 2019, MOL GENET GENOM MED, V7, DOI 10.1002/mgg3.581
  32. Kruszka P, 2017, AM J MED GENET A, V173, P2323, DOI 10.1002/ajmg.a.38362
  33. Linglart L, 2020, AM J MED GENET C, V184, P73, DOI 10.1002/ajmg.c.31765
  34. Lutz JC, 2020, J CRANIO MAXILL SURG, V48, P242, DOI 10.1016/j.jcms.2020.01.011
  35. Malaquias AC, 2012, AM J MED GENET A, V158A, P2700, DOI 10.1002/ajmg.a.35519
  36. Naslavsky MS, 2017, HUM MUTAT, V38, P751, DOI 10.1002/humu.23220
  37. Nguyen KD, 2017, REV ESP MED NUCL IMA, V36, P197, DOI 10.1016/j.remn.2016.08.006
  38. Nugent DJ, 2018, J BLOOD MED, V9, P185, DOI 10.2147/JBM.S164474
  39. Pagnamenta AT, 2019, CLIN GENET, V95, P693, DOI 10.1111/cge.13533
  40. Pierpont MEM, 2014, PEDIATRICS, V134, pE1149, DOI 10.1542/peds.2013-3189
  41. Marin LDP, 2012, OPHTHALMIC GENET, V33, P1, DOI 10.3109/13816810.2011.593606
  42. Quaio CRDC, 2012, AM J MED GENET A, V158A, P1077, DOI 10.1002/ajmg.a.35290
  43. Richards S, 2015, GENET MED, V17, P405, DOI 10.1038/gim.2015.30
  44. Rodriguez FA, 2014, J PEDIATR ENDOCR MET, V27, P305, DOI 10.1515/jpem-2013-0176
  45. Rodriguez FA, 2020, BIRTH DEFECTS RES, V112, P732, DOI 10.1002/bdr2.1659
  46. Romano AA, 2010, PEDIATRICS, V126, P746, DOI 10.1542/peds.2009-3207
  47. Siegfried A, 2017, AM J MED GENET A, V173, P1061, DOI 10.1002/ajmg.a.38108
  48. Sinnott Bridget P, 2018, BMJ Case Rep, V2018, DOI 10.1136/bcr-2017-224115
  49. Tartaglia M, 2006, AM J HUM GENET, V78, P279, DOI 10.1086/499925
  50. Tartaglia M, 2002, AM J HUM GENET, V70, P1555, DOI 10.1086/340847
  51. Tekendo-Ngongang C, 2020, BIRTH DEFECTS RES, V112, P718, DOI 10.1002/bdr2.1675
  52. Tidyman WE, 2009, CURR OPIN GENET DEV, V19, P230, DOI 10.1016/j.gde.2009.04.001
  53. VANDERBURGT I, 1994, AM J MED GENET, V53, P187, DOI 10.1002/ajmg.1320530213
  54. Villani A, 2017, CLIN CANCER RES, V23, pE83, DOI 10.1158/1078-0432.CCR-17-0631
  55. Witkowski L, 2020, MOL GENET GENOM MED, V8, DOI 10.1002/mgg3.1180
  56. WRIGHT NL, 1968, AM J DIS CHILD, V116, P367, DOI 10.1001/archpedi.1968.02100020371004
  57. Yamamoto GL, 2015, J MED GENET, V52, P413, DOI 10.1136/jmedgenet-2015-103018
  58. Zenker M, 2009, HORM RES, V72, P57, DOI 10.1159/000243782