Skip to main content
Journal of Medical Genetics logoLink to Journal of Medical Genetics
. 1980 Aug;17(4):273–276. doi: 10.1136/jmg.17.4.273

Estimates of the likelihood that a Down's syndrome child of unknown genotype is a consequence of an inherited translocation.

S G Albright, E B Hook
PMCID: PMC1048568  PMID: 6451703

Abstract

The proportions of Down's syndrome livebirths associated with a Robertsonian translocation inherited from a carrier parent were estimated from data in the New York State Chromosome Registry and in two previous publications. Indirect estimates were made in each 5-year maternal age interval; these were derived from mutation rates for these translocations and maternal age specific prevalence rates in livebirths. The proportions diminished steadily with increasing maternal age. The ranges for the seven maternal age groups from under 20 to 45 to 49 were: 1.1 to 2.8%, 1.0 to 2.7%, 0.7 to 1.8%, 0.5 to 1.3%, 0.2 to 0.4%, 0.05 to 0.1%, and 0.02 to 0.04%. Direct estimates from the observed data could only be attempted for two age groups, women under 30 and those 30 or more. For those under 30 the range in proportions was 0.9 to 1.9% and for those 30 and over, 0.2 to 0.4%. In general the lowest proportions at any age were derived from New York State data and the highest from Japanese data.

Full text

PDF
273

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Hook E. B., Chambers G. M. Estimated rates of Down syndrome in live births by one year maternal age intervals for mothers aged 20-49 in a New York State study-implications of the risk figures for genetic counseling and cost-benefit analysis of prenatal diagnosis programs. Birth Defects Orig Artic Ser. 1977;13(3A):123–141. [PubMed] [Google Scholar]
  2. Hook E. B. The ratio of de novo unbalanced translocation to 47, trisomy 21 Down syndrome. A new method for human mutation surveillance and an apparent recent change in mutation rate resulting in human interchange trisomies in one jurisdiction. Mutat Res. 1978 Dec;52(3):427–439. doi: 10.1016/0027-5107(78)90181-1. [DOI] [PubMed] [Google Scholar]
  3. Huang S. W., Emanuel I., Lo J., Liao S. K., Hsu C. C. A cytogenetic study of 77 Chinese children with Down's syndrom. J Ment Defic Res. 1967 Sep;11(3):147–152. [PubMed] [Google Scholar]
  4. Kikuchi Y., Oishi H., Tonomura A., Yamada K., Tanaka Y. Translocation Down's syndrome in Japan: its frequency, mutation rate of translocation and parental age. Jinrui Idengaku Zasshi. 1969 Sep;14(2):93–106. [PubMed] [Google Scholar]
  5. POLANI P. E., HAMERTON J. L., GIANNELLI F., CARTER C. O. CYTOGENETICS OF DOWN'S SYNDROME (MONGOLISM). 3. FREQUENCY OF INTERCHANGE OF TRISOMICS AND MUTATION RATE OF CHROMOSOME INTERCHANGES. Cytogenetics. 1965;4:193–206. doi: 10.1159/000129855. [DOI] [PubMed] [Google Scholar]

Articles from Journal of Medical Genetics are provided here courtesy of BMJ Publishing Group

RESOURCES