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Updated: Aug 6, 2026

Genetic Analysis of Hereditary Transthyretin Ala97Ser Related Amyloidosis
Published on: June 9, 2018
[Hepatic cirrhosis and alpha 1-antitrypsin deficit: a family study]
J M Raya Sańchez1, E González Reimers, F J Santolaria Fernández
1Servicio de Medicina Interna, Hospital Universitario de Canarias, Tenerife.
Abstract:
Hepatic cirrhosis secondary to deficit of alpha-1 antitrypsin is an entity rarely observed among the adult population. We describe the clinical and histological characteristics of a patient with PiZZ phenotype, affected by an hepatic cirrhosis of this etiology, as well as the analytical and phenotypical study of his close relatives, all of which presented a type-Z mutation.
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