Results 21 to 30 of about 3,080 (230)

A Novel SCNN1B Mutation in a Neonate With Systemic Pseudohypoaldosteronism Type 1: Case Report. [PDF]

Clin Case Rep
ABSTRACT Early recognition of PHA1B in neonates with persistent hyperkalemia and hyponatremia is important for timely intervention. Genetic testing confirms the diagnosis, guiding long‐term management. This case highlights a novel SCNN1B mutation, expanding the genetic spectrum and emphasizing the need for lifelong monitoring to prevent life ...
Bahadoran E, Saffari F, Moghbelinejad S.
europepmc   +2 more sources

Prevalence of and factors associated with Na + /K + imbalances in a population of children hospitalized with febrile urinary tract infection. [PDF]

Eur J Pediatr
We aimed to assess the prevalence of and factors associated with Na + /K + imbalances in children hospitalized for febrile urinary tract infection (fUTI). This retrospective Italian multicenter study included children aged 18 years or younger (median age
Marzuillo P, Guarino S, Annicchiarico Petruzzelli L, Brugnara M, Corrado C, Di Sessa A, Malgieri G, Pennesi M, Scozzola F, Taroni F, Pasini A, La Scola C, Montini G, CAKUT-UTI study group of the Italian Society of Pediatric Nephrology.   +13 more
europepmc   +3 more sources

Familial hypoaldosteronism [PDF]

, 2020
INSERM
openaire   +2 more sources

Hyporeninenmic Hypoaldosteronism [PDF]

, 2020
National Cancer Institute
openaire   +2 more sources

Selective hypoaldosteronism

The American Journal of Medicine, 1975
Michael F. Michelis, H.Victor Murdaugh
openaire   +2 more sources

Pseudo-hypoaldosteronism secondary to infantile urinary tract infections: role of ultrasound

Italian Journal of Pediatrics, 2022
Background The biochemical hallmarks of transient pseudo-hypoaldosteronism associated with a pyelonephritis include hyponatremia, hyperkalemia, and acidosis.
Noemi Graziano, Carlo Agostoni, Francesca Chiaraviglio, Céline Betti, Arianna Piffer, Mario G. Bianchetti, Gregorio P. Milani   +6 more
doaj   +1 more source

Apparent mineralocorticoid excess - A rare cause of endocrine hypertension

Indian Pediatrics Case Reports, 2022
Background: Endocrine causes of hypertension constitute a very small percentage of patients with secondary hypertension. Apparent mineralocorticoid excess (AME) is a rare genetic form of young-onset secondary hypertension.
Sonali Verma, Preeti Dabadghao, Amita Moirangthem   +2 more
doaj   +1 more source

Chronic adrenal insufficiency in children and adolescents (part 1)

Лечащий Врач, 2021
The review article contains up-to-date information on the etiology, pathogenesis, clinical features, and genetic diagnosis of chronic adrenal insufficiency in children and adolescents. Diseases associated with hypocorticism are described.
V. V. Smirnov, L. I. Bikbaeva
doaj   +1 more source

Hyperkalaemia secondary to suspected transient hyporeninaemic hypoaldosteronism in a dog (in a dog) [PDF]

Veterinary Record Case Reports, Volume 13, Issue 3, September 2025.
Abstract A 12‐year‐7‐month‐old, female, entire beagle dog was presented to a referral hospital in England for a 10‐day history of tachypnoea and lethargy. Angiostrongylus vasorum ELISA test was positive, and the patient was started on fenbendazole. One week later, it became lethargic, anorexic, polyuric and polydipsic, and it was diagnosed with an open
Mary Lucas, Francesca Venier
openalex   +2 more sources

Hypoaldosteronism syndrome in children and adolescents

Лечащий Врач, 2021
The review article describes the current data on the etiology, pathogenesis, clinical features, genetic diagnosis, and treatment tactics for hypoaldosteronism in children and adolescents. Phenotypic signs typical for this syndrome are described.
V. V. Smirnov, A. E. Saparova
doaj   +1 more source