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 235 free, full-text research articles on human participants. First 3 results:

Primary Autosomal Recessive Distal Renal Tubular Acidosis Caused by a Common Homozygous SLC4A1 Mutation in Two Lao Families.
 

Author(s): Eujin Park, Vilaphone Phaymany, Eun Sang Yi, Sommanikhone Phangmanixay, Hae Il Cheong, Yong Choi

Journal:

 

Primary distal renal tubular acidosis (dRTA) caused by mutations of the SLC4A1 gene, which encodes for erythroid and kidney isoforms of anion exchanger, shows marked difference in inheritance patterns and clinical features in different parts of the world. While the disease shows autosomal ...

Last Updated: 31 Dec 1969

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An in vitro splicing assay reveals the pathogenicity of a novel intronic variant in ATP6V0A4 for autosomal recessive distal renal tubular acidosis.
 

Author(s): Tomohiko Yamamura, Kandai Nozu, Yuya Miyoshi, Keita Nakanishi, Junya Fujimura, Tomoko Horinouchi, Shogo Minamikawa, Nobuo Mori, Rika Fujimaru, Koichi Nakanishi, Takeshi Ninchoji, Hiroshi Kaito, Taniguchi-Ikeda Mariko, Ichiro Morioka, Masafumi Matsuo, Kazumoto Iijima

Journal:

 

Autosomal recessive distal renal tubular acidosis (dRTA) is a rare hereditary disease caused by pathogenic variants in the ATP6V0A4 gene or ATP6V1B1 gene, and characterized by hyperchloremic metabolic acidosis with normal anion gap, hypokalemia, hypercalciuria, hypocitraturia and ...

Last Updated: 31 Dec 1969

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A child with distal (type 1) renal tubular acidosis presenting with progressive gross motor developmental regression and acute paralysis.
 

Author(s): Randula Ranawaka, Kavinda Dayasiri, Manoji Gamage

Journal:

 

Distal (Type 1) renal tubular acidosis (dRTA) is characterized by inability to secrete hydrogen irons from the distal tubule. The aetiology of dRTA is diverse and can be either inherited or acquired. Common clinical presentations of dRTA in the paediatric age group include polyuria, ...

Last Updated: 31 Dec 1969

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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 20 free, full-text review articles on human participants. First 3 results:

Hyperammonemia in Distal Renal Tubular Acidosis: A New Case and Review of the Literature.
 

Author(s): Kai-Hsiang Hsu, Chi-Hui Cheng, Min-Hua Tseng, Jen-Fu Hsu, Reyin Lien, Peng-Hong Yang

Journal: Pediatr Neonatol. 2015 Dec;56(6):432-4.

 

Last Updated: 31 Dec 1969

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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: 31 Dec 1969

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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: 31 Dec 1969

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Clinical Trial Information This information is provided by ClinicalTrials.gov

Study Evaluating Subjects With Distal Renal Tubular Acidosis
 

Status: Not yet recruiting

Condition Summary: Distal Renal Tubular Acidosis

 

Last Updated: 29 Aug 2018

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Incidence of Renal Tubular Acidosis in Nephrology Unit in Assiut University Childern Hospital
 

Status: Not yet recruiting

Condition Summary: Renal Tubule Acidosis

 

Last Updated: 30 Aug 2017

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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: 24 Nov 2016

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