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Dermatoglyphics and Turner Syndrome*

Published online by Cambridge University Press:  01 August 2014

R. A. Pfeiffer  and
W. Kiera
R. A. Pfeiffer
Affiliation:
Kinderklinik der Westfalischen Wilhelms-Universität, Münster
W. Kiera
Affiliation:
Kinderklinik der Westfalischen Wilhelms-Universität, Münster

Summary

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Dermatoglyphics of 81 females with Turner's syndrome are analysed with regard to the cytogenetic findings and they are compared with the data from normal relatives of both sex. The quantitative traits (total ridge count, a-b ridge count, atd angle) are shifted to an elevation of the means. Centric patterns on the hypothenar area as well as a longitudinal alignment of the main lines and transverse creases are found rather frequently. Previous studies are confirmed.

Type
Research Article
Information
Acta geneticae medicae et gemellologiae: twin research , Volume 17 , Issue 3 , July 1968 , pp. 507 - 522
Copyright
Copyright © The International Society for Twin Studies 1968

Footnotes

*

Die cytogenetischen Untersuchungen wurden mit Unterstützung der Deutschen Forschungsgemeinschaft durchgeführt.

References

Literatur

Abel, W. (1937). Über Störungen der Papillarmuster. I. Gestörte Papillarmuster in Verbindung mit einigen körperlichen und geistigen Anomalien. Z. Morph. Anthrop., 36: 1.Google Scholar
Almeida, J.C. C. de et al. (1962). Sindrome de Turner: apresentacao de un caso com estudio dos cromosomos e das impressoes palmares. Arg. Brasil Endocr., 11: 23.Google Scholar
Alter, M. (1965). Is hyperploidy of sex chromosomes associated with reduced total finger ridge count? Amer. J. Hum. Genet., 17: 473.Google Scholar
Barthe, P. (1963). Kongenitale Nackenblasen, ein besonderes Krankheitsbild. Ann. Paediat. (Basel), 201: 125.Google Scholar
Bishop, P.M. F. et al. (1960). Turner's syndrome and allied conditions. Mem Soc. Endocr., 7: 162.Google Scholar
Bonnevie, K. (1932). Zur Mechanik der Papillar-Musterbildung. II. Anomalien der menschlichen Fingerund Zchenbeeren, uebst Diskussion über die Natur der hier wirksamen Epidermis-polster. Ronx' Arch. Eutn. Mech., 126: 378.Google Scholar
Cummins, H., Midlo, Ch. (1961). Finger Prints, Palms and Soles. Dover Publ. Inc., New York.Google Scholar
Edwards, J.H. et al. (1866). Monozygotic twins of different sex. J. Med. Genet., 3: 117.Google Scholar
Forbes, A.P. (1964). Fingerprints and palm prints (dermatoglyphics) and palmar-flexion creases in gonadal dysgenesis, pseudohypoparathyroidism and Klinefelter's syndrome. New Engl. J. Med., 270: 1268.Google Scholar
Holt, S.B. (1952/1953). Genetics of dermal ridges; inheritance of total ridge count. Ann. Eugen., 17: 140.CrossRefGoogle Scholar
Holt, S.B. (1955/1956). Genetics of dermal ridges: frequency distributions of total finger ridge-count. Ann. Hum. Genet. (London), 20: 159.Google Scholar
Holt, S.B. (1961). Quantitative genetics of finger-print patterns. Brit. Med. Bull., 17: 247.Google Scholar
Holt, S.B. (1963). Current advances in our knowledge of the inheritance of variations in finger-prints. Proc. Sec. Internat. Congr. Hum. Genet., Rome 1961.Google Scholar
Holt, S.B. Lindsten, J. (1964). Dermatoglyphic anomalies in Turner's syndrome. Ann. Hum. Genet. (London), 28: 87.Google Scholar
Kiera, W. (1967). Hand- und Fingerleistenmuster beim Turner-Syndrom. Inaug. Diss., Münster.Google Scholar
Mikkelsen, M. et al. (1963). XO-XX mosaicism in a pair of presumable monozygotic twins with different phenotypes. Cytogenetics, 2: 86.Google Scholar
Penrose, L.S. (1967). Finger-print pattern and the sex chromosomes. Lancet, 1: 298.Google Scholar
Penrose, L.S. (1963). Finger-prints, palms and chromosomes. Nature (London), 197: 933.CrossRefGoogle Scholar
Singh, R.P., Carr, D. H. (1966). The anatomy and histology of XO human embryos and fetuses. Anat. Rec., 155: 369.Google Scholar
Turpin, R., Lejeune, J. (1965). Les Chromosomes Humains. Gauthkr-Villars, Paris.Google Scholar
Uchida, I.A. et al. (1964). Dermatoglyphics associated with the XXYY chromosome complement. Amer J. Hum. Genet., 16: 284.Google Scholar
Uchida, I.A. Soltan, H.C. (1963). Evaluation of dermatoglyphics in medical genetics. Pediat. Clin. N. Amer., 10: 409.Google Scholar
Weninger, M., Navratil, L. (1957). Die Vierfingerfurche in ätiologischer Betrachtung. Mitt. Anthrop. Ges. Wien, 87: 1.Google Scholar