"Dermatoglyphics" (from ancient Greek derma=skin, glyph=carving) is the scientific study of fingerprints, lines, mounts, and shapes of hands, while some regard dermatoglyphics as a variant on the pseudoscience of palmistry, there is a considerable scientific literature on linkage of genetic aberrations to finger prints.
Dermatoglyphic and Genetic Aberrations:
47,XXY or XXY (Klinefelter's syndrome): Excess of arches on digit 1, more frequent ulnar loops on digit 2, overall fewer whorls, lower ridge counts for loops and whorls as compared with controls, and significant reduction of the total finger ridge count.
Noonan syndrome: Increased frequency of whorls on fingertips, and the axial triradius t, as in Turner syndrome, is more often in position t' or t" than in controls. Increased incidence of the single transverse palmar crease.
Trisomy 21 (Down syndrome): People with Down syndrome have a finger print pattern with mainly ulnar loops, and a significantly different angle between the triradia a, t and d (the 'adt angle'). Other differences often include a single transverse palmar crease ("Simian line") (in 50%), and patterns in the hypothenar and interdigital areas, lower ridge counts along digital midlines, especially in little fingers, which corresponds to finger shortening in those with Down syndrome. There is less variation in dermatoglyphic patterns between people with Down syndrome than between controls, and dermatoglyphic patterns can be used to determine correlations with congenital heart defects in individuals with Down syndrome by examining the left hand digit ridge count minus the right hand digit ridge count, and the number of ridges on the fifth digit of the left hand.
- "Publications: Hands & Dermatoglyphics". Retrieved 15 April 2015.
- Komatz Y, Yoshida O (1976). "Finger patterns and ridge counts of patients with Klinefelter's syndrome (47, XXY) among the Japanese". Hum Hered 26 (4): 290–7. doi:10.1159/000152816. PMID 976997.
- Viswanathan G, Singh H, Ramanujam P (2002). "Dermatoglyphic analysis of palmar print of blind children from Bangalore.". J. Ecotoxicol. Environ. Monit. 12: 49–52.
- Viswanathan G, Singh H, Ramanujam P (2002). "[Dermatoglyphic analysis of finger tip print patterns of blind children from Bangalore.]". J. Ecotoxicol. Environ. Monit. 12: 73–75.
- Lugassy, Jennie, et al. "Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis: two allelic ectodermal dysplasias caused by dominant mutations in KRT14." The American Journal of Human Genetics 79.4 (2006): 724-730.
- Rott H, Schwanitz G, Reither M (1975). "[Dermatoglyphics in Noonan's syndrome (author's transl)]". Acta Genet Med Gemellol (Roma) 24 (1–2): 63–7. PMID 1224924.
- Rajangam S, Janakiram S, Thomas I (1995). "Dermatoglyphics in Down's syndrome". J Indian Med Assoc 93 (1): 10–3. PMID 7759898.
- Mglinets V (1991). "[Relationship between dermatoglyphic variability and finger length in genetic disorders: Down's syndrome]". Genetika 27 (3): 541–7. PMID 1830282.
- Mglinets V, Ivanov V (1993). "[Bilateral symmetry of the dermatoglyphic characteristics in Down's syndrome]". Ontogenez 24 (3): 98–102. PMID 8355961.
- Durham N, Koehler J (1989). "Dermatoglyphic indicators of congenital heart defects in Down's syndrome patients: a preliminary study". J Ment Defic Res 33 (4): 343–8. doi:10.1111/j.1365-2788.1989.tb01485.x. PMID 2527997.
- Reed T, Reichmann A, Palmer C (1977). "Dermatoglyphic differences between 45,X and other chromosomal abnormalities of Turner syndrome". Hum Genet 36 (1): 13–23. doi:10.1007/BF00390431. PMID 858621.
- Padfield, C. J., M. W. Partington, and N. E. Simpson. "The Rubinstein-Taybi syndrome." Archives of disease in childhood 43.227 (1968): 94.
- Fananas, L., P. Moral, and J. Bertranpetit. "Quantitative dermatoglyphics in schizophrenia: study of family history subgroups." Human biology (1990): 421-427.
|This article has not been added to any categories. Please help out by adding categories to it so that it can be listed with similar articles. (April 2015)|