Hostname: page-component-77c89778f8-vpsfw Total loading time: 0 Render date: 2024-07-16T15:55:02.010Z Has data issue: false hasContentIssue false

Chromosomal and Dermatoglyphic Changes in Twins

Published online by Cambridge University Press:  01 August 2014

W. A. Yarema*
Affiliation:
Division of Medical Genetics, Department of Medicine, The Johns Hopkins University School of Medicine, Baltimore, Md
D. S. Borgaonkar
Affiliation:
Division of Medical Genetics, Department of Medicine, The Johns Hopkins University School of Medicine, Baltimore, Md
*
St. Elizabeth Medical Center, 601 Miami Blwd. West, Dayton, Ohio 45408, USA

Summary

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

A review of 15 chromosomally abnormal twin pairs indicates that finger and hallucal patterns of the affected twin are more similar to other patients than to the normal cotwin.

Correlation coefficients of TFRC and atd angle differences tend to remain similar in spite of the presence of chromosome abnormality in the cotwin. This supports the use of dermatoglyphic analysis as a means for diagnosing twin zygosity. Correlation coefficients of intrapair TFRC and atd angle differences in 25 control MZ twin pairs shows good agreement in zygosity determinations, when compared to results obtained by blood group and clinical observation studies.

In a series of 155 female and 142 male MZ twin pairs, TFRC and atd angle differences plotted on a graph against the frequency of occurrence illustrate that the range of variation is greater among females. Further study of a large series of twin pairs, however, is necessary to determine whether this is an effect of lyonization or the alteration of the polygenic complex of dermal configuration by the X chromosome.

Type
Research Article
Copyright
Copyright © The International Society for Twin Studies 1970

References

Bertrand, L., Barjon, P., Lejeune, J., Emberger, J. M., Janbon, Ch. (1966). Syndrome de Klinefelter chez deux jumeaux monozygotes avec dermatoglyphes dissemblables. Ann. Endocr. (Paris), 27: 830835.Google Scholar
Dekaban, A. (1965). Twins, probably monozygotic: one mongoloid with 48 chromosomes, the other normal. Cytogenetics, 4: 227239.CrossRefGoogle ScholarPubMed
De Wolff, E., Schaerer, K., Lejeune, J. (1963). Contribution à l'étude des jumeaux mongoliens. Un cas de monozygotisme hétérocaryote. Helv. Paediat. Acta, 17: 3031.Google Scholar
Edwards, J. H., Dent, T., Kahn, J. (1966). Monozygotic twins of different sex. J. Med. Genet., 3: 117123.CrossRefGoogle ScholarPubMed
Ford, N., Frumkin, S. (1942). Monozygosity in mongoloid twins. Amer. J. Dis. Child., 63: 647858.Google Scholar
Gedda, L. (1961). Twins in History and Science. Charles C Thomas, Springfield.Google Scholar
Holt, S. B., Lindsten, J., (1964). Dermatoglyphic anomalies in Turner's syndrome. Ann. Hum. Genet., 28: 87100.CrossRefGoogle ScholarPubMed
Lamy, M., Frezal, J., de Grouchy, J., Kelly, J. (1956). Le nombre de dermatoglyphes dans un échantillon de jumeaux. Ann. Hum. Genet., 21: 374396.CrossRefGoogle Scholar
Lyon, M. F. (1961 a). Gene action in the X chromosome of the mouse (Mus musculus L.). Nature (London), 190: 372.CrossRefGoogle Scholar
Lyon, M. F. (1961 b). Genetic factors on the X chromosome. Lancet, 2: 434.CrossRefGoogle Scholar
McKusick, V. A. (1969). Human Genetics. Prentice-Hall, Englewood Cliffs, N. J. Google Scholar
Nance, W. E., Uchida, I. (1964). Turner's syndrome, twinning and an unusual variant of glucose-6-phosphate dehydrogenase. Amer J. Hum. Genet., 16: 380392.Google Scholar
Nielsen, J. (1967). Inheritance in monozygotic twins. Lancet, 2: 717718.CrossRefGoogle Scholar
Nowakowski, H., Lenz, W., Bergmah, S., Reitalu, J. (1963). Chromosome studies in identical twins with Klinefelter's syndrome. Path. Biol. (Paris), 11: 1239.Google Scholar
Osborne, R. H., De George, F. V. (1959). Genetic Basis of Morphological Variation. Harvard University Press, Cambridge, Mass.CrossRefGoogle Scholar
Penrose, L. S., Smith, G. F. (1966). Down's Anomaly. Churchill Ltd., London.Google Scholar
Shine, I. B., Corney, G. (1966). Turner's syndrome in monozygotic twins. J. Med. Genet., 3: 124128.CrossRefGoogle ScholarPubMed
Smith, R. T. (1965). A comparison of socioenvironmental factors in monozygotic and dizygotic twins, testing an assumption. In: Methods and Goals in Huma n Behavior Genetics. Academic Press, Inc., New York.Google Scholar
Smith, S. M., Penrose, L. S. (195). Monozygotic and dizygotic twin diagnosis. Ann. Hum. Genet., 19: 273289.CrossRefGoogle Scholar
Turner, H. H., Zanartu, J. (1962). Ovarian dysgenesis in identical twins: discrepancy between nuclear chromatic pattern in somatic cells and in blood cells. J. Clin. Endocr., 22: 660665.CrossRefGoogle Scholar
Uchida, I. A., Soltan, H. C. (1963). Evaluation of dermatoglyphics in medical genetics. Pediat. Clin. N. Amer., 10: 409422.CrossRefGoogle Scholar
Vanderberg, S. C., McKusick, V. A., McKusick, A. B. (1962). Twin data in support of the Lyon hypothesis. Nature (London), 4827: 505506.Google Scholar
Walker, N. F. (1957). Inkless methods of finger, palm and sole printing. J. Pediat., 50: 2730.CrossRefGoogle ScholarPubMed