Amniotic trisomy 11 mosaicism - Is it a benign finding?

Prenatal Diagnosis

Volumn 26, Issue 9, 2006, Pages 778-781

  Basel Vanagaite, Lina ^a,b   Davidov, Bella ^a   Friedman, Jane ^a   Yeshaya, Yosefa ^a   Magal, Nurit ^b   Drasinover, Valerie ^b   Shohat, Mordechai ^a,b  

^a RABIN MEDICAL CENTER   (Israel)

^b TEL AVIV UNIVERSITY   (Israel)

Author keywords

Amniocentesis; Normal outcome; Trisomy 11 mosaicism

Indexed keywords

AMNION CELL; AMNIOTIC FLUID CELL; ARTICLE; CHROMOSOME 11; DELIVERY; ECHOGRAPHY; EPITHELIUM CELL; FIBROBLAST; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; KARYOTYPE; LYMPHOCYTE; PERINATAL PERIOD; PRENATAL SCREENING; PRIORITY JOURNAL; SEX CHROMOSOME MOSAICISM; TRISOMY; UMBILICAL CORD BLOOD; UNIPARENTAL DISOMY;

ADULT; AMNIOCENTESIS; CHROMOSOMES, HUMAN, PAIR 11; FEMALE; HUMANS; MALE; MOSAICISM; PREGNANCY; PROGNOSIS; TRISOMY;

EID: 33749476295     PISSN: 01973851     EISSN: 10970223     Source Type: Journal    
DOI: 10.1002/pd.1501     Document Type: Article

References (12)

1. Daniel A, Wu Z, Darmanian A, et al. 2004. Issues arising from the prenatal diagnosis of some rare trisomy mosaics-the importance of cryptic fetal mosaicism. Prenat Diagn 24: 524-536.
2. Hahnemann JM, Vejerslev LO. 1997. European collaborative research on mosaicism in CVS [EUCROMIC]-Fetal and extrafetal cell lineages in 192 gestations with CVS mosaicism involving single autosomal trisomy. Am J Med Genet 70: 179-187.
3. Hassold T. 1982. Mosaic trisomies in human spontaneous abortions. Hum Genet 61: 31-35.
4. Henry I, Bonaiti-Pellie C, Chehensse V, et al. 1991. Uniparental paternal disomy in a genetic cancer-predisposing syndrome. Nature 351: 665-667.
5. Hsu LYF. 1992. Chromosomal disorders. In Medicine of the Fetus and the Mother, Reece EA, Hobbins JC, Mahoney MJ, Petrie RH (eds). JB Lippincott: Philadelphia, PA: 426-454.
6. Hsu LYF, Kaffe S, Perlis TE. 1987. Trisomy 20 mosaicism in prenatal diagnosis-a review and update. Prenat Diagn 7: 581-598.
7. Hsu LYF, Kaffe S, Perlis TE. 1991. A revisit of trisomy 20 mosaicism in prenatal diagnosis: an overview of 103 cases. Prenat Diagn 11: 715.
8. Hsu LYF, Kaffe S, Jenkins EC, et al. 1992. Proposed guidelines for diagnosis of mosaicism and pseudomosaicism studies. Prenat Diagn 12: 555-573.
9. Hsu LYF, Yu MT, Neu RL, et al. 1997. Rare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20, and 21: Karyotype/phenotype correlations. Prenat Diagn 17: 201-242.
10. Kalousek DK, Dill FJ. 1983. Chromosomal mosaicism confined to the placenta in human conceptions. Science 221: 665-667.
11. Robinson WP, McGillivray B, Lewis ME, et al. 2005. Prenatally detected trisomy 20 mosaicism. Prenat Diagn 25: 239-244.
12. Rooney DE. 2001. Human Cytogenetics: Constitutional Analysis a Practical Approach, (3rd edn). Oxford University Press: Oxford; 33-128.