Prenatal diagnosis of low level trisomy 15 mosaicism: Review of the literature

Clinical Genetics

Volumn 53, Issue 4, 1998, Pages 286-292

  Zaslav, A L ^a   Fallet, S ^a   Brown, S ^b   Ebert, R ^a   Fleischer, A ^c   Valderama, E ^c   Fox, J E ^a  

^a SCHNEIDER CHILDREN'S HOSPITAL   (United States)

^b Dept of Obstetrics and Gynecology   (United States)

^c LONG ISLAND JEWISH MEDICAL CENTER   (United States)

Author keywords

Prenatal diagnosis; Trisomy 15; Trisomy 15 mosaicism; True mosaicism

Indexed keywords

ADULT; AMNIOCENTESIS; ARTICLE; CASE REPORT; CHROMOSOME 15; CHROMOSOME MOSAICISM; CONTROLLED STUDY; FEMALE; FETUS; FETUS LUNG; FLUORESCENCE IN SITU HYBRIDIZATION; HEART; HEART RIGHT VENTRICLE DYSPLASIA; HUMAN; HUMAN TISSUE; HYPOPLASIA; INTERPHASE; INTRAUTERINE GROWTH RETARDATION; KARYOTYPE; MEIOSIS; METAPHASE; PLACENTA; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; THERAPEUTIC ABORTION; TISSUE; TRISOMY; ULTRASOUND; UMBILICAL ARTERY;

EID: 0031959602     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1399-0004.1998.tb02698.x     Document Type: Article

References (20)

1. Gimelli G, Cuoco C, Porro E. Prenatal Diagnosis, fetal pathology and cytogenetic analysis of 46,XX/47.XX, + 15 mosaic. Prenat Diag 1983: 3: 75-79.
2. Bennett CP, Davis T, Seller MJ. Trisomy 15 mosaicism in an IVF fetus. J Med Genet 1992: 29: 745-746.
3. Sundberg K, Brocks V, Jacobsen JR, Beck B. True trisomy 15 mosaicism detected at amniocentesis at 12 weeks of gestation and fetal echocardiography. Prenat Diag 1994: 14: 559-563.
4. Rocklin ML, Elder FFB, Ledbetter DH, Christian S, Huang B, Rosenberg H, Sheppard C, Wilkins I. True fetal trisomy 15 mosaicism with maternal uniparental disomy. Am J Hum Genet 1994: 55: A286.
5. Markovic VD, Chitayat DA, Ritchie SM, Chodakowski BA, Hutton EM. Trisomy 15 mosaic derived from trisomic conceptus: report of a case and a review. Am J Med Genet 1996: 61: 363-370.
6. Christian SL, Smith ACM, Macha M, Black SH, Elders FFB, Johnson JMP, Resta RG, Surti U, Suslak L, Verp MS, Ledbetter DH. Prenatal diagnosis of uniparental disomy 15 following trisomy 15 mosaicism. Prenat Diag 1996: 16: 323-332.
7. Stallard R, Sommer A. Trisomy 15 in a mosaic doubly aneuploid two year old. Am J Hum Genet 1989: 45: A92.
8. Lahdetie J, Lakkala T. Mosaic trisomy 15 found at amnio-centesis. Prenat Diag 1992: 12: 551-552.
9. Fryns JP, Kleczkowska A, Lagae L, Kenis H, Van Den Berghe H. A specific phenotype associated with trisomy 15 mosaicism. Ann Genet 1993: 36 (2): 129-131.
10. Milunsky JM, Wyandt HE, Huang XL, Kang XZ, Elias ER, Milunsky A. Trisomy 15 mosaicism and uniparental disomy (UPD) in a liveborn infant. Amer J Med Genet 1996: 61: 269-273.
11. Seabright MA. A rapid banding technique for human chromosomes. Lancet 1971: ii: 971-972.
12. Hsu LY, Kaffe S, Jenkins EC, Alonso L, Benn PA, David K, Hirschhorn K, Lieber E, Shanske A, Shapiro LR, Schutta E, Warburton D. Proposed guidelines for diagnosis of mosaicism in amniocytes based on data derived from chromosome mosaicism and pseudomosaicism studies. Prenat Diag 1992: 12: 555-573.
13. Weber JL, May PE. Abundant class of human DNA polymorphisms which can be typed using the representative chain reaction. Am J Hum Genet 1989: 44: 388-396.
14. Kalousek DK, Howard-Peebles PN, Olson SB, Barrett IJ, Dorfmann A, Black SH, Schulman JD, Wilson RD. Confirmation of CVS mosaicism in term placenta and high frequency of intrauterine growth retardation association with confined placental mosaicism. Prenat Diag 1991: 11: 743-750.
15. Hsu L, Yu M, Neu R, Van Dyke D, Benn P, Bradshaw C, Shaffer L, Higgins R, Khodr G, Morion C, Wang H, Brothman A, Chadwick D, Disteche C, Jenkins L, Kalousek D, Pantzar T, Wyatt P. The significance of rare trisomy mosaicism diagnosed in aminocytes. Am J Hum Genet 1996: 59 (4): A202.
16. Robinson WP, Lorda-Sanchez I, Malcolm S, Langlois S, Schuffenhauer S, Knoblauch H, Horsthemke B, Schinzel AA. Increased parental ages and uniparental disomy 15: A paternal age effect. Eur J Hum Genet 1993: 1: 280-286.
17. Zaragoza MV, Jacobs PA, James RS, Rogan P, Sherman S, Hassold T. Nondisjunction of human acrocentric chromosomes. Studies of 432 trisomic fetuses and liveborns. Hum Genet 1994: 94: 411-417.
18. Coldwell S, Fitzgerald B, Semmens JM, Ede R, Bateman C. A case of trisomy of chromosome 15. J Med Genet 1981: 18: 146-148.
19. Kuller JA, Laifer SA. Trisomy 15 associated nonimmune hydrops. Am J Perinatol 1991: 8: 39-40.
20. Romero RR, Pilu G, Jeanty P, Ghidini A, Hobbins JC. Prenatal diagnosis of congenital anomalies. Norwalk, Connecticut: Appleton and Lange, 1988: 387-390.