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Questions and Answers
What is the name of the disease that causes people to be born without fingerprints?
At what stage of fetal development do fingerprints typically form?
What is a common skin problem associated with adermatoglyphia?
Which of the following can cause acquired loss of dermatoglyphics?
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What is the name of the gene associated with isolated congenital adermatoglyphia?
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How is isolated congenital adermatoglyphia inherited?
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What is a potential complication of adermatoglyphia due to impaired sweating?
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Which of the following dermatological conditions can cause acquired loss of dermatoglyphics?
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What is a non-dermatological cause of acquired adermatoglyphia?
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Fingerprints develop with the unborn baby, when the fetus is about ______ weeks old.
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Adermatoglyphia is a disease that affects not only your fingers but also the ______ of your hands and the ______ of your feet.
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The formation of fingerprints is influenced by multiple ______ and environmental factors.
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People with adermatoglyphia often don’t ______ normally.
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Loss of fingerprints can be ______ or acquired.
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The isolated congenital cases usually have a point mutation in the ______ site of a 3' exon of the gene.
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Dermatological conditions such as ______ can be responsible for acquired loss of dermatoglyphics in a few digits or in all fingers.
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Potent ______ can cause epi‐dermal ridge atrophy.
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Adermatoglyphia is a disease that affects several skin areas, including the ______ and the feet.
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