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  2. Dermatoglyphics - Wikipedia

    en.wikipedia.org/wiki/Dermatoglyphics

    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.

  3. Adermatoglyphia - Wikipedia

    en.wikipedia.org/wiki/Adermatoglyphia

    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. Five extended families worldwide are known to be affected by this condition.

  4. Congenital malformations of the dermatoglyphs - Wikipedia

    en.wikipedia.org/wiki/Congenital_malformations...

    This cutaneous condition article is a stub. You can help Wikipedia by expanding it.

  5. What exactly causes skin tags? Here's what dermatologists ...

    www.aol.com/exactly-causes-skin-tags-heres...

    But, if it feels like one just appeared out of nowhere, you might be wondering what causes them in the first place. The reality is that we don’t always know why skin tags form, ...

  6. Fingerprint - Wikipedia

    en.wikipedia.org/wiki/Fingerprint

    The human skin itself, which is a regenerating organ until death, and environmental factors such as lotions and cosmetics, pose challenges when fingerprinting a human. Following the death of a human, the skin dries and cools. Fingerprints of dead humans may be obtained during an autopsy. [40]

  7. Absence of fingerprints-congenital milia syndrome - Wikipedia

    en.wikipedia.org/wiki/Absence_of_fingerprints...

    Absence of fingerprints-congenital milia syndrome, also known simply as Baird syndrome is an extremely rare autosomal dominant genetic disorder which is characterized by a lack of fingerprints and the appearance of blisters and facial milia soon after birth. [2] It has been described in ten families worldwide. [3] [4]

  8. Kabuki syndrome - Wikipedia

    en.wikipedia.org/wiki/Kabuki_syndrome

    Child displaying typical facial phenotype of Kabuki syndrome. Specific symptoms for Kabuki syndrome vary, with large differences between affected individuals. [3] Most people with Kabuki syndrome have distinctive facial features that include arched eyebrows, long eyelashes, elongated eyelids with lower lids that turn out, prominent ears, a flat tip of the nose and a downward slant to the mouth.

  9. Polydactyly - Wikipedia

    en.wikipedia.org/wiki/Polydactyly

    This is mainly caused by the fact that there is a generally normal function of these patients’ hands following ablation with collateral ligament reconstruction. [12] In a study on 27 patients undergoing surgical excision for Type A ulnar polydactyly, only one complication was noted in the form of an infection. [ 47 ]

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