| Title: |
Identification of compound heterozygous patients with primary hyperoxaluria type 1: clinical evaluations and in silico investigations |
| Authors: |
Houda Kanoun; Faiçal Jarraya; Bayen Maalej; Amina Lahiani; Hichem Mahfoudh; Fatma Makni; Jamil Hachicha; Faiza Fakhfakh |
| Source: |
BMC Nephrology, Vol 18, Iss 1, Pp 1-10 (2017) |
| Publisher Information: |
BMC |
| Publication Year: |
2017 |
| Collection: |
Directory of Open Access Journals: DOAJ Articles |
| Subject Terms: |
Primary hyperoxaluria type 1; AGT; AGXT gene; Mutation; Compound heterozygous; Diseases of the genitourinary system. Urology; RC870-923 |
| Description: |
Background Primary hyperoxaluria type 1 (PH1) is an autosomal recessive inherited disorder of glyoxylate metabolism in which excessive oxalates are formed by the liver and excreted by the kidneys. Calcium oxalate crystallizes in the urine, leading to urolithiasis, nephrocalcinosis, and consequent renal failure if treatment is not initiated promptly. Mutations in the AGXT gene which encodes the hepatic peroxisomal enzyme alanine:glyoxylate aminotransferase are responsible of PH1. In the present work, we aimed to analyze AGXT gene and in silico investigations performed in four patients with PH1 among two non consanguineous families. Methods Exhaustive gene sequencing was performed after PCR amplification of coding exons and introns boundaries. Bioinformatic tools were used to predict the impact of AGXT variants on gene expression as well as on the protein structure and function. Results Direct sequencing of all exons of AGXT gene revealed the emergence of multiple mutations in compound heterozygous state in the two studied families. Two patients were compound heterozygous for the c.731 T > C, c.32C > T, c.1020A > G and c.33_34insC and presented clinically with recurrent urinary tract infection, multiple urolithiasis and nephrocalcinosis under the age of 1 year and a persistent hyperoxaluria at the age of diagnosis. The two other patients presenting a less severe phenotypes were heterozygous for c.731 T > C and homozygous for the c.32C > T and c.1020A > G or compound heterozygous for c.26C > A and c.65A > G variants. Conclusion In Summary, we provided relevance regarding the compound heterozygous mutations in non consanguineous PH1 families with variable severity. |
| Document Type: |
article in journal/newspaper |
| Language: |
English |
| Relation: |
http://link.springer.com/article/10.1186/s12882-017-0719-y; https://doaj.org/toc/1471-2369; https://doaj.org/article/01c505f1ebc94f27b43724793dc95d09 |
| DOI: |
10.1186/s12882-017-0719-y |
| Availability: |
https://doi.org/10.1186/s12882-017-0719-y; https://doaj.org/article/01c505f1ebc94f27b43724793dc95d09 |
| Accession Number: |
edsbas.F6EFA44F |
| Database: |
BASE |