Skip to Accessibility Menu
Skip to Login
Skip to Content
Skip to Footer
Menu
Open search
Search
Accessibility
Log in
Congenital analbuminemia
What is Congenital analbuminemia?
Congenital analbuminemia (CAA) is characterized by the absence or dramatic reduction of circulating human serum albumin (HSA).
Inheritance type
Autosomal recessive
Prevalence
Worldwide: <1 in 1,000 000
Age of Onset
Infancy
Neonatal
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on
"https://www.orphadata.com"
. Data version 1.3.16 / 4.1.7.