Αρχειοθήκη ιστολογίου

Τετάρτη 21 Οκτωβρίου 2020

Fortuitous Discovery of Hereditary Xanthinuria.

ola Kala shared this article with you from Inoreader
Icon for Clinical Laboratory

Fortuitous Discovery of Hereditary Xanthinuria.

Clin Lab. 2020 Oct 01;66(10):

Authors: Biaz A, Tazi S, Bouhsain S, Chemsi M, Dami A, Machtani-Idrissi SE

Abstract
Hereditary xanthinuria was the first inherited purine metabolism disorder described. It is a rare pathology, which is most often asymptomatic and whose incidence is therefore underestimated. We report the case of a patient with an undetectable level of uric acid in the blood, discovered during a systematic biological assessment. This case report recalls the existence of this rare metabolic disorder, which is usually benign, but can lead to complications, and the importance of considering an abnormality of the purine cycle when discovering a hypo-uricemia.

PMID: 33073950 [PubMed - in process]

View on the web

Δεν υπάρχουν σχόλια:

Δημοσίευση σχολίου

Medicine by Alexandros G. Sfakianakis,Anapafseos 5 Agios Nikolaos 72100 Crete Greece,00302841026182,00306932607174,alsfakia@gmail.com,

Αναζήτηση αυτού του ιστολογίου

! # Ola via Alexandros G.Sfakianakis on Inoreader