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Condition

Adermatoglyphia

Diseases of the Skin and Subcutaneous Tissue

Adermatoglyphia is an extremely rare genetic disorder that prevents the development of fingerprints, so affected people are born without the ridged patterns normally found on the fingertips. Five extended families worldwide are known to be affected by the condition. Professor Peter Itin informally nicknamed it immigration delay disease after his first patient had trouble traveling to the United States because he had no fingerprints for identification. The condition is recorded here as a documented curiosity of human genetics and skin development, with the lead source describing its rarity and its practical everyday consequence rather than any wider medical picture.

Facts
Classification
Body System
Integumentary System 1
ICD-10 Chapter
XVII: Congenital Malformations, Deformations and Chromosomal Abnormalities 2
Communicable or Non-communicable
Non-Communicable 1
Causative Agent
Causative Agent (category)
Genetic / Hereditary 1
Sources
1. Adermatoglyphia (Wikipedia)
  • Lead paragraph
    extremely rare genetic disorder
  • Lead paragraph [body-system]
    prevents the development of fingerprints
  • Lead: disease category
    Adermatoglyphia is an extremely rare genetic disorder that prevents the development of fingerprints.
View the Source
2. World Health Organization ICD-10: ICD-10 Version:2019 - Q80-Q89
World Health Organization ICD-10Category Q82.8
Quote, Category Q82.8
Q82.8 Other specified congenital malformations of skin
View the Source
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