Results 11 to 20 of about 19,301 (213)

Systemic lupus erythematosus associated with type 4 renal tubular acidosis: a case report and review of the literature

Journal of Medical Case Reports, 2011
Introduction Type 4 renal tubular acidosis is an uncommon clinical manifestation of systemic lupus erythematosus and has been reported to portend a poor prognosis.
Young Larry, Garcia-Buitrago Monica, Lanfranco Julio, Morgan Nadia, Porteous Haldane, Lenz Oliver   +5 more
doaj   +1 more source

Renal Tubular Acidosis and Immune Checkpoint Inhibitor Therapy: An Immune-Related Adverse Event of PD-1 Inhibitor—A Report of 3 Cases

Kidney Medicine, 2020
The main cause of acute kidney injury in patients receiving immune checkpoint inhibitors (ICIs) is acute interstitial nephritis. However, as their use continues to increase, other kidney manifestations are being described.
Sandra M. Herrmann, Mariam P. Alexander, Michael F. Romero, Ladan Zand   +3 more
doaj   +1 more source

Distal Renal Tubular Acidosis in Adolescence with Severe Growth Retardation and Nephrocalcinosis

Journal of Nepal Medical Association, 2012
Chronic acidosis is an important, often overlooked cause of growth retardation. Here we present the case of a girl with distal renal tubular acidosis who had visited multiple hospitals before the diagnosis was made.
M R Sigdel, M P Kafle, K B Raut
doaj   +1 more source

SGLT2 Inhibitor Use for Treatment of Hypocitraturia in a Distal Renal Tubular Acidosis

Kidney Medicine
5-Amino salicylic acid (5-ASA) is a known culprit for the development of tubulointerstitial nephritis. Together with impaired kidney function, tubulointerstitial nephritis can lead to specific tubular malfunctions including distal renal tubular acidosis.
Stefan Scherr, Sara H. Ksiazek, Christoph Schwarz, Marcus D. Säemann   +3 more
doaj   +1 more source

Medullary nephrocalcinosis, distal renal tubular acidosis and polycythaemia in a patient with nephrotic syndrome

BMC Nephrology, 2012
Background Medullary nephrocalcinosis and distal renal tubular acidosis are closely associated and each can lead to the other. These clinical entities are rare in patients with nephrotic syndrome and polycythaemia is an unusual finding in such patients ...
Karunarathne Suneth, Udayakumara Yapa, Govindapala Dumitha, Fernando Harshini   +3 more
doaj   +1 more source

A case of severe metabolic acidosis during pregnancy

Clinical Case Reports, 2019
Key Clinical Message Renal tubular acidosis (RTA) is a disorder that impairs renal acid‐base regulation leading to normal anion gap metabolic acidosis. It is rare to encounter this entity during pregnancy. Pregnancy can worsen renal tubular acidosis (RTA)
Mo'tasem Alkhasoneh, Jennifer Jacobs, Gurwant Kaur   +2 more
doaj   +1 more source

Distal renal tubular acidosis a rarely diagnosed cause of failure to thrive: A report of three cases

Ibom Medical Journal, 2007
SUMMARY Three cases of distal renal tubular acidosis aged between 6 - 12weeks are described. The presenting features included lethargy, refusal to feed, marked periodic respiration, vomiting and recurrent episode of unexplained metabolic acidosis.
Adeleke SI, Asani MO
doaj   +1 more source

Familial distal renal tubular acidosis

Journal of International Medical Research, 2021
We report the case of a family in which two sisters have distal renal tubular acidosis (dRTA). Familial dRTA is a rare disorder, with both autosomal dominant and recessive transmission. This is a report of familial dRTA from China.
Lihong Zhang, Bei Xu, Ya Niu, Yajuan Wang, Hui Tang   +4 more
doaj   +1 more source

Distal renal tubular acidosis and severe hypokalemia: a case report and review of the literature

Journal of Medical Case Reports, 2019
Background Distal renal tubular acidosis is a relatively infrequent condition with complex pathophysiology that can present with life-threatening electrolyte abnormalities.
George Vasquez-Rios, David John Westrich, Isaac Philip, John C. Edwards, Stephanie Shieh   +4 more
doaj   +1 more source

A Rare Form of Microcephalic Primordial Dwarfism due to NSMCE2 Deficiency (Seckel Syndrome Type 10): A Report of Macular Involvement

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Biallelic variants in NSMCE2 (MMS21), which encodes the SUMO E3 ligase subunit of the SMC5/6 chromatin‐maintenance complex, have recently been implicated in microcephalic primordial dwarfism (MPD), corresponding to Seckel syndrome type 10 (OMIM #617246).
Cristina Peduto, Céline Huber, Clément Paya, Isabelle Audo, Nathalie Boddaert, Valérie Cormier‐Daire   +5 more
wiley   +1 more source