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Adermatoglyphia information


Adermatoglyphia
Other namesImmigration delay disease
Adermatoglyphia is inherited in an autosomal dominant manner

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.[1][2]

The disorder was informally nicknamed "immigration delay disease" by Professor Peter Itin after his first patient had trouble traveling to the U.S. without any fingerprints for identification.[3]

  1. ^ Reference, Genetics Home. "Adermatoglyphia". Genetics Home Reference. Retrieved 2020-07-07.
  2. ^ "Adermatoglyphia disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials". www.malacards.org. Retrieved 2020-07-07.
  3. ^ "The family with no fingerprints". BBC News. 2020-12-26. Retrieved 2020-12-27.

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