Renal tubular acidosis

Common Name(s)

Renal tubular acidosis

Description for this condition is not yet available.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Renal tubular acidosis" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Renal tubular acidosis" returned 194 free, full-text research articles on human participants. First 3 results:

A role for VAX2 in correct retinal function revealed by a novel genomic deletion at 2p13.3 causing distal Renal Tubular Acidosis: case report.
 

Author(s): Elizabeth E Norgett, Anthony Yii, Katherine G Blake-Palmer, Mostafa Sharifian, Louise E Allen, Abdolhamid Najafi, Ariana Kariminejad, Fiona E Karet Frankl

Journal:

 

Distal Renal Tubular Acidosis is a disorder of acid-base regulation caused by functional failure of α-intercalated cells in the distal nephron. The recessive form of the disease (which is usually associated with sensorineural deafness) is attributable to mutations in ATP6V1B1 or ...

Last Updated: 13 Jun 2015

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Clinical evaluation of Chinese patients with primary distal renal tubular acidosis.
 

Author(s): Chunli Zhang, Hong Ren, Pingyan Shen, Yaowen Xu, Wen Zhang, Weiming Wang, Xiao Li, Yuhuan Ma, Nan Chen

Journal: Intern. Med.. 2015 ;54(7):725-30.

 

Distal renal tubular acidosis (dRTA) is a hyperchloremic metabolic acidosis disorder characterized by a normal anion gap with abnormal urinary hydrogen (H(+)) excretion. At present, there are few available reports regarding the clinical status of primary dRTA. The primary objective ...

Last Updated: 2 Apr 2015

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Distal renal tubular acidosis with nerve deafness secondary to ATP6B1 gene mutation.
 

Author(s): Parvathina Sriram Naveen, Lokanatha Srikanth, Katari Venkatesh, Potukuchi Venkata Gurunadha Krishna Sarma, Naga Sridhar, Chennu Krishnakishore, Yanala Sandeep, Yadla Manjusha, Vishnubhotla Sivakumar

Journal: Saudi J Kidney Dis Transpl. 2015 Jan;26(1):119-21.

 

Autosomal recessive distal renal tubular acidosis (dRTA) is associated with mutation in the ATP6B1 gene encoding the B1 subunit of H + -ATPase, one of the key membrane transporters for net acid excretion of α-intercalated cells of medullary collecting ducts. Sensori-neural deafness ...

Last Updated: 12 Jan 2015

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Reviews from the PubMed Database

Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Renal tubular acidosis" returned 18 free, full-text review articles on human participants. First 3 results:

Everything you need to know about distal renal tubular acidosis in autoimmune disease.
 

Author(s): Tim Both, Robert Zietse, Ewout J Hoorn, P Martin van Hagen, Virgil A S H Dalm, Jan A M van Laar, Paul L A van Daele

Journal: Rheumatol. Int.. 2014 Aug;34(8):1037-45.

 

Renal acid-base homeostasis is a complex process, effectuated by bicarbonate reabsorption and acid secretion. Impairment of urinary acidification is called renal tubular acidosis (RTA). Distal renal tubular acidosis (dRTA) is the most common form of the RTA syndromes. Multiple pathophysiologic ...

Last Updated: 23 Jul 2014

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Structure, function, and regulation of the SLC4 NBCe1 transporter and its role in causing proximal renal tubular acidosis.
 

Author(s): Ira Kurtz, Quansheng Zhu

Journal: Curr. Opin. Nephrol. Hypertens.. 2013 Sep;22(5):572-83.

 

There has been significant progress in our understanding of the structural and functional properties and regulation of the electrogenic sodium bicarbonate cotansporter NBCe1, a membrane transporter that plays a key role in renal acid-base physiology. The NBCe1 variant NBCe1-A mediates ...

Last Updated: 6 Aug 2013

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Distal renal tubular acidosis: a hereditary disease with an inadequate urinary H⁺ excretion.
 

Author(s): Laura Escobar, Natalia Mejía, Helena Gil, Fernando Santos

Journal: Nefrologia. 2013 ;33(3):289-96.

 

Distal renal tubular acidosis (dRTA) or RTA type I is characterised by reduced H+ hydrogen ions and ammonium urinary excretion. In children affected by dRTA there is stunted growth, vomiting, constipation, loss of appetite, polydipsia and polyuria, nephrocalcinosis, weakness ...

Last Updated: 28 May 2013

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Symptoms, Diagnosis, and Treatment

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Clinical Trial Information This information is provided by ClinicalTrials.gov

Renal Tubular Acidosis in Incident Renal Transplant Recipients
 

Status: Recruiting

Condition Summary: Renal Transplant Disorder

 

Last Updated: 29 May 2012

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Influence of Polymorphisms in the ATP6V1 Gene of the V-ATPase on the Development of Incomplete Distal Renal Tubular Acidosis
 

Status: Recruiting

Condition Summary: Acidosis, Renal Tubular; Nephrolithiasis; Vacuolar Proton-Translocating ATPases

 

Last Updated: 28 Jul 2015

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