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Article

Congenital analbuminemia associated with compound heterozygous novel nucleotide variations in a young adult with coronary thrombosis

Yessine Amri ; Sana Aboulkacem ; Rym Dabboubi ; Manel Ayoub ; Oussema Lamine ; Mariem Othmani ; Zied Aouni ; Taieb Messaoud ; Chakib Mazigh |

Dans Annales de Biologie Clinique (Vol. 81, n° 2, mars-avril 2023)

Congenital analbuminemia (CAA) is a very rare genetic disorder characterized by a significant reduced or even complete absence of human serum albumin. Our data describe the clinical features and laboratory results of a case confirmed by muta[...]

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