FEATURES OF GILBERT'S SYNDROME IN PATIENTS WITH DIFFERENT GENOTYPES UGT1AI.

S A KurilovichE G NemtsovaM V KruchininaV N Maximov

Published in: Eksperimental'naia i klinicheskaia gastroenterologiia = Experimental & clinical gastroenterology (2018)

Patients with asthenic constitution and the stigma dysplasia of connective tissue have to be examined by the presence of mutations rs8175347 gene UGT1A1. The carrier not only homozygous but with the heterozygous variant mutations may require changes in the interpretation of symptoms, lifestyle, medication, etc.

Keyphrases

mental health
metabolic syndrome
cardiovascular disease
physical activity
artificial intelligence
early onset
hiv aids
mental illness
healthcare
weight loss
genome wide
social support
case report
adverse drug
gene expression
machine learning
sleep quality
transcription factor
depressive symptoms