LAUSR

About LAUSR
Donate
Contact Us

Follow us:

You are not signed in:

Sign Up!


   Articles with "type renal" as a keyword



Pseudohypoaldosteronism and acquired renal aldosterone resistance with hyperkalemic type IV renal tubular acidosis in 2 cats

Sign Up to like & get
recommendations! Published in 2024 at "Journal of Veterinary Internal Medicine"

DOI: 10.1111/jvim.17098

Abstract: This report describes the diagnosis and treatment of aldosterone resistance (AR) and acquired hyperkalemic type IV renal tubular acidosis (RTA) in 2 cats comparable to acquired pseudohypoaldosteronism in people. One cat developed AR from chronic… read more here.

Keywords: tubular acidosis; renal tubular; hyperkalemic type; type renal ... See more keywords

Alport’s syndrome with type 4 renal tubular acidosis

Sign Up to like & get
recommendations! Published in 2017 at "BMJ Case Reports"

DOI: 10.1136/bcr-2017-220146

Abstract: This case report details a 51-year-old man with Alport’s syndrome resulting in chronic nephritis with stable renal function and sensorineural deafness. The patient was being investigated for persistently raised potassium refractory to dietary and pharmacological… read more here.

Keywords: syndrome type; alport syndrome; tubular acidosis; renal tubular ... See more keywords

Acid–Base Imbalance in Pseudohypoaldosteronism Type 1 in Comparison With Type IV Renal Tubular Acidosis

Sign Up to like & get
recommendations! Published in 2022 at "Journal of the Endocrine Society"

DOI: 10.1210/jendso/bvac147

Abstract: Abstract Context Pseudohypoaldosteronism type 1 (PHA1) has been treated as a genetic variant of type IV renal tubular acidosis (RTA), leading to the conception that PHA1 develops hyperchloremic acidosis with a normal anion gap (AG).… read more here.

Keywords: acidosis; type renal; pseudohypoaldosteronism type; acid base ... See more keywords
Photo from archive.org

Novel Type of Renal Amyloidosis Derived from Apolipoprotein-CII.

Sign Up to like & get
recommendations! Published in 2017 at "Journal of the American Society of Nephrology : JASN"

DOI: 10.1681/asn.2015111228

Abstract: Amyloidosis is characterized by extracellular deposition of misfolded proteins as insoluble fibrils. Most renal amyloidosis cases are Ig light chain, AA, or leukocyte chemotactic factor 2 amyloidosis, but rare hereditary forms can also involve the… read more here.

Keywords: renal amyloidosis; novel type; amyloidosis; apo cii ... See more keywords