Novel compound heterozygous SLC4A1 mutations in Thai patients with autosomal recessive distal renal tubular acidosis

Background: Mutations in the SLC4A1 gene have been found to cause either autosomal dominant (AD) or autosomal recessive (AR) distal renal tubular acidosis (dRTA). The SLC4A1 mutations causing AD dRTA were reported in white patients, whereas those associated with AR dRTA were often found in Southeast...

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Main Authors: Suchai Sritippayawan, Achra Sumboonnanonda, Somkiat Vasuvattakul, Thitima Keskanokwong, Nunghathai Sawasdee, Atchara Paemanee, Peti Thuwajit, Prapon Wilairat, Sumalee Nimmannit, Prida Malasit, Pa Thai Yenchitsomanus
Other Authors: Mahidol University
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Published: 2018
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/21610
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spelling th-mahidol.216102018-07-24T10:50:22Z Novel compound heterozygous SLC4A1 mutations in Thai patients with autosomal recessive distal renal tubular acidosis Suchai Sritippayawan Achra Sumboonnanonda Somkiat Vasuvattakul Thitima Keskanokwong Nunghathai Sawasdee Atchara Paemanee Peti Thuwajit Prapon Wilairat Sumalee Nimmannit Prida Malasit Pa Thai Yenchitsomanus Mahidol University Medicine Background: Mutations in the SLC4A1 gene have been found to cause either autosomal dominant (AD) or autosomal recessive (AR) distal renal tubular acidosis (dRTA). The SLC4A1 mutations causing AD dRTA were reported in white patients, whereas those associated with AR dRTA were often found in Southeast Asia. Here, the authors report additional novel SLC4A1 mutations in 3 patients with AR dRTA from 2 unrelated Thai families. Methods: The patients and members of their families were clinically studied. Red cell morphology and sulfate influx were examined. The SLC4A1 gene was screened, analyzed, and confirmed for mutations by molecular genetic techniques. Results: In the first family, the patient had dRTA, rickets, failure to thrive, nephrocalcinosis, and hypokalemic-hyperchloremic metabolic acidosis with a urine pH level of 7.00. He had novel compound heterozygous SLC4A1 G701D/S773P mutations, inherited from clinically normal heterozygous mother and father. In the second family, the patient and his sister had dRTA and Southeast Asian ovalocytosis (SAO) with different clinical severity. The patient had proximal muscle weakness, rickets, nephrocalcinosis, hypokalemia, normal anion gap metabolic acidosis, and urine pH level of 6.80. His sister was asymptomatic but the urine pH level could not be lowered to below 5.50 after a short acid load. Both siblings had compound heterozygous SLC4A1 SAO/R602H mutations. Conclusion: Two novel compound heterozygous SLC4A1 G701D/S773P and SAO/R602H mutations were identified in Thai patients with AR dRTA. © 2004 by the National Kidney Foundation, Inc. 2018-07-24T03:50:22Z 2018-07-24T03:50:22Z 2004-07-01 Article American Journal of Kidney Diseases. Vol.44, No.1 (2004), 64-70 10.1053/j.ajkd.2004.03.033 02726386 2-s2.0-3042817603 https://repository.li.mahidol.ac.th/handle/123456789/21610 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=3042817603&origin=inward
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Medicine
spellingShingle Medicine
Suchai Sritippayawan
Achra Sumboonnanonda
Somkiat Vasuvattakul
Thitima Keskanokwong
Nunghathai Sawasdee
Atchara Paemanee
Peti Thuwajit
Prapon Wilairat
Sumalee Nimmannit
Prida Malasit
Pa Thai Yenchitsomanus
Novel compound heterozygous SLC4A1 mutations in Thai patients with autosomal recessive distal renal tubular acidosis
description Background: Mutations in the SLC4A1 gene have been found to cause either autosomal dominant (AD) or autosomal recessive (AR) distal renal tubular acidosis (dRTA). The SLC4A1 mutations causing AD dRTA were reported in white patients, whereas those associated with AR dRTA were often found in Southeast Asia. Here, the authors report additional novel SLC4A1 mutations in 3 patients with AR dRTA from 2 unrelated Thai families. Methods: The patients and members of their families were clinically studied. Red cell morphology and sulfate influx were examined. The SLC4A1 gene was screened, analyzed, and confirmed for mutations by molecular genetic techniques. Results: In the first family, the patient had dRTA, rickets, failure to thrive, nephrocalcinosis, and hypokalemic-hyperchloremic metabolic acidosis with a urine pH level of 7.00. He had novel compound heterozygous SLC4A1 G701D/S773P mutations, inherited from clinically normal heterozygous mother and father. In the second family, the patient and his sister had dRTA and Southeast Asian ovalocytosis (SAO) with different clinical severity. The patient had proximal muscle weakness, rickets, nephrocalcinosis, hypokalemia, normal anion gap metabolic acidosis, and urine pH level of 6.80. His sister was asymptomatic but the urine pH level could not be lowered to below 5.50 after a short acid load. Both siblings had compound heterozygous SLC4A1 SAO/R602H mutations. Conclusion: Two novel compound heterozygous SLC4A1 G701D/S773P and SAO/R602H mutations were identified in Thai patients with AR dRTA. © 2004 by the National Kidney Foundation, Inc.
author2 Mahidol University
author_facet Mahidol University
Suchai Sritippayawan
Achra Sumboonnanonda
Somkiat Vasuvattakul
Thitima Keskanokwong
Nunghathai Sawasdee
Atchara Paemanee
Peti Thuwajit
Prapon Wilairat
Sumalee Nimmannit
Prida Malasit
Pa Thai Yenchitsomanus
format Article
author Suchai Sritippayawan
Achra Sumboonnanonda
Somkiat Vasuvattakul
Thitima Keskanokwong
Nunghathai Sawasdee
Atchara Paemanee
Peti Thuwajit
Prapon Wilairat
Sumalee Nimmannit
Prida Malasit
Pa Thai Yenchitsomanus
author_sort Suchai Sritippayawan
title Novel compound heterozygous SLC4A1 mutations in Thai patients with autosomal recessive distal renal tubular acidosis
title_short Novel compound heterozygous SLC4A1 mutations in Thai patients with autosomal recessive distal renal tubular acidosis
title_full Novel compound heterozygous SLC4A1 mutations in Thai patients with autosomal recessive distal renal tubular acidosis
title_fullStr Novel compound heterozygous SLC4A1 mutations in Thai patients with autosomal recessive distal renal tubular acidosis
title_full_unstemmed Novel compound heterozygous SLC4A1 mutations in Thai patients with autosomal recessive distal renal tubular acidosis
title_sort novel compound heterozygous slc4a1 mutations in thai patients with autosomal recessive distal renal tubular acidosis
publishDate 2018
url https://repository.li.mahidol.ac.th/handle/123456789/21610
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