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
ICD-10 ChapterXVII: Congenital Malformations, Deformations and Chromosomal Abnormalities 2 Communicable or Non-communicable Causative Agent
Causative Agent (category) 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 Source2. World Health Organization ICD-10: ICD-10 Version:2019 - Q80-Q89
World Health Organization ICD-10Category Q82.8Quote, Category Q82.8
Q82.8 Other specified congenital malformations of skin
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