Skip to main content
Log in

Cardiac malformation of partial trisomy 7p/monosomy 18p and partial trisomy 18p/monosomy 7p in siblings as a result of reciprocal unbalanced malsegregation—and review of the literature

  • Original Article
  • Published:
European Journal of Pediatrics Aims and scope Submit manuscript

Abstract

We report two unbalanced translocations involving the short arms of chromosomes 7 and 18 due to a balanced translocation 7;18 in the mother. Karyotyping and fluorescence in situ hybridization analysis of the female fetus revealed an unbalanced subtelomeric translocation (karyotype 46,XX,der(18)t(7;18)(p22.3;p11.32)mat resulting in a partial trisomy 7p and a partial monosomy 18p. Array comparative genomic hybridization (CGH) detected a 4.44-Mb heterozygous duplication at 7p22.3 to 7p22.1 and a 0.178-Mb heterozygous deletion at 18p11.32. Clinical characteristics comprised a mildly stenotic bicuspid aortic valve and a small aortic arch without coarctation. The patient’s older brother displayed a reciprocal version of her chromosomal aberration (46,XY,der(7)t(7;18)(p22;p11.32) resulting in a partial monosomy 7p and a partial trisomy 18p. Array CGH revealed a 4.75-Mb heterozygous deletion at 7p22.3p22.1 and a 0.579-Mb duplication at 18p11.32. He presented with tetralogy of Fallot, cleft palate, microcephalus without craniosynostosis, growth retardation, ptosis of the right eyelid, right-sided renal agenesis, unilateral cryptorchism, and mental retardation. In this report, we present the clinical phenotype in patients with aberrations of chromosomes 7p and 18p and reviewed the literature to summarize cardiovascular malformations in these patients.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2

Similar content being viewed by others

References

  1. Arens YH, Toutain A, Engelen JJ, Offermans JP, Hamers AJ, Schrander JJ, Pulles-Heintzberger CP et al (2000) Trisomy 7 p; report of 2 patients and literature review. Genet Couns 11:347–354

    PubMed  CAS  Google Scholar 

  2. Brenk CH, Prott E-C, Trost D, Hoischen A, Walldorf C, Radlschwimmer B, Wieczorek D et al (2007) Towards mapping phenotypical traits in 18 p- syndrome by array-based comparative genomic hybridisation and fluorescent in situ hybridisation. Eur J Hum Genet 15:35–44

    Article  PubMed  CAS  Google Scholar 

  3. Brewer C, Holloway S, Zawalnyski P, Schinzel A, FitzPatrick D (1999) A chromosomal duplication map of malformations: regions of suspected haplo- and triplolethality—and tolerance of segmental aneuploidy—in humans. Am J Hum Genet 64:1702–1708

    Article  PubMed  CAS  Google Scholar 

  4. Cai T, Yu P, Tagle DA, Xia J (1999) Duplication of 7 p 21.2-pter due to material 7p;21q translocation. Implications for critical segment assignment in the 7p duplication syndrome. Am J Med Genet 86:305–311

    Article  PubMed  CAS  Google Scholar 

  5. Cantú JM, Rivas F, Ruiz C, Barajas LO, Moller M, Rivera H (1985) Trisomy 7 p due to a mosaic normal/dir dup(7)(p13-p22). Syndrome delineation, critical segment assignment, and a comment on duplications. Ann Genet 28:254–257

    PubMed  Google Scholar 

  6. Carlo B, Lina A, Vincenzo Z (1982) Deletions of the short arm of chromosome 7 without craniosynostosis. Clin Genet 21:348–349

    Article  PubMed  CAS  Google Scholar 

  7. Cattanach BM, Shibata H, Hayashizaki Y, Townsend KM, Ball S, Beechey CV (1998) Association of a redefined proximal mouse chromosome 11 imprinting region and U2afbp-rs/U2af1-rs1 expression. Cytogenet Cell Genet 80:41–47

    Article  PubMed  CAS  Google Scholar 

  8. Chotai KA, Brueton LA, van Herwerden L, Garrett C, Hinkel GK, Schinzel A, Mueller RF et al (1994) Six cases of 7p deletion: clinical, cytogenetic, and molecular studies. Am J Med Genet 51:270–276

    Article  PubMed  CAS  Google Scholar 

  9. Chui JV, Weisfeld-Adams JD, Tepperberg J, Mehta L (2011) Clinical and molecular characterization of chromosome 7p22.1 microduplication detected by array CGH. Am J Med Genet A 155A(10):2508–2511

    PubMed  Google Scholar 

  10. Cohen MM, Storm DF, Capraro VJ (1972) A ring chromosome (No. 18) in a cyclops. Clin Genet 3:249–252

    Article  PubMed  CAS  Google Scholar 

  11. Cox H, Stewart H, Hall L, Donnai D (2002) Phenotypic spectrum of interstitial 7p duplication in mosaic and non mosaic forms. Ann J Med Genet 109:306–310

    Article  Google Scholar 

  12. Crawfurd MD, Kessel I, Liberman M, McKeown JA, Mandalia PY, Ridler MA (1979) Partial monosomy 7 with interstitial deletions in two infants with differing congenital abnormalities. J Med Genet 16:453–460

    Article  PubMed  CAS  Google Scholar 

  13. Debiec Rychter M, Overhauser J, Kaluzewski B, Jakubowski I, Truszczak B, Wilson W, Skorski M et al (1990) De novo direct tandem duplication of the short arm of chromosome 7 (p21.1-p14.2). Am J Med Genet 36:316–320

    Article  PubMed  CAS  Google Scholar 

  14. Dennehey BK, Gutches DG, McConkey EH, Krauter KS (2004) Inversion, duplication, and changes in gene context are associated with human chromosome 18 evolution. Genomics 83:493–501

    Article  PubMed  CAS  Google Scholar 

  15. Digilio MC, Marino B, Giannotti A, Di Donato R, Dallapiccola B (2000) Heterotaxy with left atrial isomerism in a patient with deletion 18p. Am J Med Genet 94:198–200

    Article  PubMed  CAS  Google Scholar 

  16. El Kalla S, Mathews AR, Menon NS (1992) Del(18p) syndrome with complex tetralogy of Fallot in an infant with 45,X,t(Y;18)(q12;q11.2). Am J Med Genet 42(5):665–666

    Article  PubMed  Google Scholar 

  17. Faust J, Habedank M, Nieuwenhuijsen C (1976) The 18 p-syndrome. Report of four cases. Eur J Pediatr 123:59–66

    Article  PubMed  CAS  Google Scholar 

  18. Franz HB, Schliphacke M, Niemann G, Mielke G, Backsch C (1996) De novo direct tandem duplication of a small segment of the short arm of chromosome 7 (p21-22.1). Clin Genet 50:426–429

    Article  PubMed  CAS  Google Scholar 

  19. Friedrich U, Lyngbye T, Oster J (1975) A girl with karyotype 46, XX, del(7)(qter- > p15:). Hum Genet 26:161–165

    Article  CAS  Google Scholar 

  20. Gallego C, Grant J, Mikhail F, Barger C, Robin N (2010) Use of array comparative genome hybridization in orofacial clefting. J Craniofac Surg 21:1591–1594

    Article  PubMed  Google Scholar 

  21. Giraud F, Hartung M, Mattei JF, Passeron P, Coignet J (1971) 46, XY-45, X mosaicism and 18p- deletion. Ann Genet 14:59–62

    PubMed  CAS  Google Scholar 

  22. Hinkel GK, Tolkendorf E, Bergan J (1988) 7p-deletion syndrome. Monatsschr Kinderheilkd 136:824–827

    PubMed  CAS  Google Scholar 

  23. Joyce CA, Sharp A, Walker JM, Bullman H, Temple IK (1999) Duplication of 7p 12.1-p13, including GRB10 and IGFBP 1, in a mother and daughter with feature of Silver-Russell syndrome. Hum Genet 105:273–280

    Article  PubMed  CAS  Google Scholar 

  24. Kleczkowska A, Decock P, van den Berghe H, Fryns JP (1994) Borderline intelligence and discrete craniofacial dysmorphism in an adolescent female with partial trisomy 7 p due to a de novo tandem duplication 7 (p15.1-p21.3). Genet Couns 5:393–397

    PubMed  CAS  Google Scholar 

  25. Kozma C, Haddad BR, Meck JM (2000) Trisomy 7p resulting from 7p 15;9 p24 translocation: report of a new case and review of associated medical complications. Am J Med Genet 91:286–290

    Article  PubMed  CAS  Google Scholar 

  26. Leach NT, Chudoba I, Stewart TV, Holmes LB, Weremovicz S (2007) Maternally inherited duplication of chromosome 7, dup(7)(p11.2p12), associated with mild cognitive deficit without features of Silver-Russell-Syndrome. Am J Med Genet A 143A:1489–1493

    Article  PubMed  Google Scholar 

  27. Li S, Tuck-Muller CM, Martínez JE, Rowley ER, Chen H, Wertelecki W (1998) Prenatal detection of de novo duplication of the short arm of chromosome 18 confirmed by fluorescence in situ hybridization (FISH). Am J Med Genet 80(5):487–490

    Article  PubMed  CAS  Google Scholar 

  28. McPherson E, Hall JG, Hickman R, Gong BT, Norwood TH, Hoehn H (1976) Chromosome 7 short arm deletion and craniosynostosis a 7p- syndrome. Hum Genet 35:117–123

    Article  PubMed  Google Scholar 

  29. Megarbane A, Le Loc HM, Elghezal H, Joly G, Gosset P, Souraty N, Samaras L et al (2001) Pure partial 7p trisomy including the TWIST, HOXA, and GLI3 genes. J Med Genet 38:178–182

    Article  PubMed  CAS  Google Scholar 

  30. Monk D, Wakeling EL, Proud V, Hitchins M, Abu-Amero SN, Stanier P, Preece MA et al (2000) Duplication of 7p11.2 p13, including GRB10, in Silver–Russell Syndrome. Am J Hum Genet 66:36–46

    Article  PubMed  CAS  Google Scholar 

  31. Moog U, Engelen JJ, de Die-Smulders CE, Albrechts JC, Loneus WH, Haagen AA, Raven EJ et al (1994) Partial trisomy of the short arm of chromosome 18 due to inversion duplication and direct duplication. Clin Genet 46:423–429

    Article  PubMed  CAS  Google Scholar 

  32. Movahhedian HR, Kane HA, Borgaonkar D, McDermott M, Septimus S (1991) Heart disease associated with deletion of the short arm of chromosome 18. Del Med J 63:285–289

    PubMed  CAS  Google Scholar 

  33. Nazarenko SA, Ostroverkhova NV, Vasiljeva EO, Nazarenko LP, Puzyrev VP, Malet P, Nemtseva TA (1999) Keratosis pilaris and ulerythema ophryogenes associated with an 18p deletion caused by a Y/18 translocation. Am J Med Genet 85:179–182

    Article  PubMed  CAS  Google Scholar 

  34. Papadopoulou E, Sifakis S, Sarri C, Gyftodimou J, Liehr T, Mrasek K, Kalmanti M et al (2006) A report of pure 7p duplication syndrome and review of the literature. Am J Med Genet A 140A:2802–2806

    Article  Google Scholar 

  35. Pearl W (1989) Heart disease associated with deletion of the short arm of chromosome 18. Pediatr Cardiol 10:174–176

    Article  PubMed  CAS  Google Scholar 

  36. Redha MA, Krishna Murthy DS, Al-Awasi SA, AL-Sulaiman IS, Sabry MA, El-Bahey SA, Farag TI (1996) De novo direct duplication 7p (p11.2-pter) in an Arab child with MCA/MR syndrome. Trisomy 7p a delineated syndrome. Ann Genet 39:5–9

    PubMed  CAS  Google Scholar 

  37. Reish O, Berry SA, Dewald G, King RA (1996) Duplication of 7p. Further delineation of the phenotype and restriction of the critical region to the distal part of the short arm. Ann J Med Genet 61:21–25

    Article  CAS  Google Scholar 

  38. Richards EG, Zaveri HP, Wolf VL, Kang SH, Scott DA (2011) Delineation of a less than 200 kb minimal deleted region for cardiac malformations on chromosome 7p22. Am J Med Genet A 155A(7):1729–1734

    PubMed  Google Scholar 

  39. Rivera H, Bobadilla I, Rolon A, Kunz I, Grolla JA (1998) Intrachromosomal triplication of distal 7p. J Med Genet 35:78–80

    Article  PubMed  CAS  Google Scholar 

  40. Rodríguez L, Liehr T, Mrasek K, Mansilla E, Martínez-Fernández ML, Garcia A, Martínez-Frías ML (2007) Small supernumerary chromosome marker generating complete and pure trisomy 18p, characterized by molecular cytogenetic techniques and review. Am J Med Genet A 143A:2727–2732

    Article  PubMed  Google Scholar 

  41. Schaefer GB, Novak K, Steele D, Buehler B, Smith S, Zaleski D, Pickering D et al (1995) Familial inverted duplication 7p. Am J Med Genet 56:184–187

    Article  PubMed  CAS  Google Scholar 

  42. Schömig-Spingler M, Schmid M, Brosi W, Grimm T (1986) Chromosome 7 short arm deletion, 7p21––pter. Hum Genet 74:323–325

    PubMed  Google Scholar 

  43. Speleman F, Craen M, Leroy J (1989) De novo terminal deletion 7p22.1–pter in a child without craniosynostosis. J Med Genet 26:528–532

    Article  PubMed  CAS  Google Scholar 

  44. Takeda K, Okamura T, Hasegawa T (1989) Sibs with tetrasomy 18p born to a mother with trisomy 18p. J Med Genet 26:195–197

    Article  PubMed  CAS  Google Scholar 

  45. Taylor KM, Wolfinger HL, Brown MG, Chadwick DL (1975) Origin of a small metacentric chromosome: familial and cytogenic evidence. Clin Genet 8:364–369

    Article  PubMed  CAS  Google Scholar 

  46. Telvi L, Bernheim A, Ion A, Fouquet F, Le Bouc Y, Chaussain JL (1995) Gonadal dysgenesis in del(18p) syndrome. Am J Med Genet 57:598–600

    Article  PubMed  CAS  Google Scholar 

  47. Turleau C (2008) Monosomy 18p. Orphanet J Rare Dis 19:3–4

    Google Scholar 

  48. Vaillaud JC, Martin J, Ayraud N (1970) A recent case of partial deletion of short arm of chromosome 18. Ann Genet 13:120–122

    PubMed  CAS  Google Scholar 

  49. Vasquez JC, Rabah R, Delius RE, Walters HL (2003) Hypoplastic left heart syndrome with intact atrial septum associated with deletion of the short arm of chromosome 18. Cardiovasc Pathol 12:102–104

    Article  PubMed  CAS  Google Scholar 

  50. Wester U, Bondeson ML, Edeby C, Annerén G (2006) Clinical and molecular characterization of individuals with 18p deletion: a genotype–phenotype correlation. Am J Med Genet A 140(11):1164–1171

    PubMed  Google Scholar 

  51. Wilson GN, Heller KB, Elterman RD, Schneider NR (1990) Partial trisomy 18 with minimal anomalies: lack of correspondence between phenotypic manifestations and triplicated loci along chromosome 18. Am J Med Genet 36:506–510

    Article  PubMed  CAS  Google Scholar 

  52. Wolff DJ, Schwartz MF, Cohen MM, Schwartz S (1993) Precise mapping of a de novo duplication 18(q21– > q22) utilizing cytogenetic, biochemical, and molecular techniques. Am J Med Genet 46:520–523

    Article  PubMed  CAS  Google Scholar 

  53. Wolpert CM, Donnelly SL, Cuccaro ML, Hedges DJ, Poole CP, Wright HH, Gilbert JR et al (2001) De novo partial duplication of chromosome 7p in a male with autistic disorder. Am J Med Genet 105:222–225

    Article  PubMed  CAS  Google Scholar 

  54. Xie CH, Yang JB, Gong FQ, Zhao ZY (2008) Patent ductus arteriosus and pulmonary valve stenosis in a patient with 18p deletion syndrome. Yonsei Med J 49:500–502

    Article  PubMed  Google Scholar 

  55. Zerres K, Schwanitz G, Gellissen K, Schroers I, Sohler R (1989) Duplication 7p de novo and literature review. Ann Genet 32:225–229

    PubMed  CAS  Google Scholar 

Download references

Conflict of interest

The authors declare that they have no conflict of interest.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Beate Schmidt.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Schmidt, B., Udink ten Cate, F., Weiß, M. et al. Cardiac malformation of partial trisomy 7p/monosomy 18p and partial trisomy 18p/monosomy 7p in siblings as a result of reciprocal unbalanced malsegregation—and review of the literature. Eur J Pediatr 171, 1047–1053 (2012). https://doi.org/10.1007/s00431-012-1682-z

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00431-012-1682-z

Keywords

Navigation