Generalized arterial calcification of infancy, abbreviated GACI, is an extremely rare genetic disorder of the blood vessels that usually appears in infants during the first six months of life. Mutations in the ENPP1 gene account for about three quarters of affected individuals, and mutations in the ABCC6 gene for roughly one in ten; in the remaining cases no causative mutation is found and the cause is unknown. It is inherited in an autosomal recessive pattern. The disease is marked by calcification of the internal elastic lamina of the arteries, which ruptures, and the resulting changes in the inner layer of the vessel wall narrow the vessel and reduce its elasticity. Many affected infants die of vaso-occlusive disease, especially of the coronary arteries.
Facts
Classification
ICD-10 ChapterXVII: Congenital Malformations, Deformations and Chromosomal Abnormalities 2 Communicable or Non-communicable Causative Agent
Causative Agent (category) Sources
1. Generalized arterial calcification of infancy (Wikipedia)
Lead, first paragraph
It is caused by mutations in the ENPP1 gene
Lead, second paragraph
generalized calcification of the arterial internal elastic lamina
Lead: disease category
Generalized arterial calcification of infancy (GACI) is an extremely rare genetic disorder.
View the Source2. World Health Organization: ICD-10 Version:2019 - Q20-Q28 Congenital malformations of the circulatory system
World Health OrganizationCategory Q28.8Quote, Category Q28.8
Q28.8 Other specified congenital malformations of
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