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Dermatoglyphics, when correlated with genetic abnormalities, aids in the diagnosis of congenital malformations at birth or soon after.. Klinefelter 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.
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Adermatoglyphia is an extremely rare genetic disorder that prevents the development of fingerprints.Five extended families worldwide are known to be affected by this condition.
In his multiple positions as an educator, Cummins taught over 5000 students. [11] Cummins worked at Vanderbilt University as a Histology instructor (1916-1917) [12] and as an assistant professor of Microscopic Anatomy from 1917 through 1919.
In orthodontics, a malocclusion is a misalignment or incorrect relation between the teeth of the upper and lower dental arches when they approach each other as the jaws close.
Richard L. Jantz is an American anthropologist. He served as the director of the University of Tennessee Anthropological Research Facility from 1998–2011 and he is the current Professor Emeritus of the Department of Anthropology at the University of Tennessee, Knoxville.
Melanism, meaning a mutation that results in completely dark skin, does not exist in humans. In humans, the amount of melanin is determined by three dominant alleles (AABBCC), and different ethnicities have varying amounts. [ 33 ]
Two-point discrimination (2PD) is the ability to discern that two nearby objects touching the skin are truly two distinct points, not one.It is often tested with two sharp points during a neurological examination [1]: 632 [2]: 71 and is assumed to reflect how finely innervated an area of skin is.