Genetic Disorders and the Fetus 2009
DOI: 10.1002/9781444314342.ch6
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Prenatal Diagnosis of Chromosomal Abnormalities through Amniocentesis

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Cited by 14 publications
(17 citation statements)
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“…21 The overall frequency of deletions that we observed (1 out of 6800) is similar to the earlier estimate by Benn and Hsu in a metanalysis of studies of newborns. 2 In both, the most frequent deletion is of terminal 4p, with a frequency of 1 out of 21 000 and only 4q34-qter, 5p and 18q11 deletions showed frequencies higher than 1 out of 50 000 -each reported in two cases. All other deletions were found only once in the entire cohort.…”
Section: Discussionmentioning
confidence: 93%
“…21 The overall frequency of deletions that we observed (1 out of 6800) is similar to the earlier estimate by Benn and Hsu in a metanalysis of studies of newborns. 2 In both, the most frequent deletion is of terminal 4p, with a frequency of 1 out of 21 000 and only 4q34-qter, 5p and 18q11 deletions showed frequencies higher than 1 out of 50 000 -each reported in two cases. All other deletions were found only once in the entire cohort.…”
Section: Discussionmentioning
confidence: 93%
“…Some laboratories have extended the testing to other autosomal trisomies . In the first trimester, this may identify pregnancies at high risk for spontaneous fetal loss, but in the second trimester, the clinical significance of a positive result is unclear . Some positive cases will be associated with confined placental mosaicism, but in rare instances, true fetal mosaicism could be present.…”
Section: General Considerations For Cfdna Screeningmentioning
confidence: 99%
“…In general, the phenotypes for each of these rare true mosaic conditions range from normal to a highly variable set of abnormalities that do not constitute well‐defined syndromes. Moreover, phenotypes cannot be accurately predicted from follow‐up cytogenetic analysis of amniotic fluid cells . A clinically significant uniparental disomy could also be present for chromosomes 6, 7, 11, 14, 15, and 20.…”
Section: General Considerations For Cfdna Screeningmentioning
confidence: 99%
“…Routine use of noninvasive prenatal diagnosis for Down syndrome as a complete replacement for current testing would therefore miss some of the other abnormalities currently identifiedthroughaprenatalsonographicexaminationandwould miss about 50% of all chromosome abnormalities now detectable through amniocentesis. 9 Balancing the benefits of noninvasive prenatal diagnosis against the more comprehensive detectioncurrentlyachievedbyinvasivetestingwouldberequired. After discussing with her physician or genetic counselor the risks and benefits of each approach, each patient would need to determine which type of testing she would prefer.…”
Section: Practical Issuesmentioning
confidence: 99%