Results 51 to 60 of about 9,796 (177)

When an Oral Lesion Uncovers Hyperparathyroidism: A Peripheral Brown Tumor Case

Clinical Case Reports, Volume 14, Issue 5, May 2026.
ABSTRACT Oral lesions may represent the first sign of an underlying systemic disease. Giant cell lesions in the oral cavity should prompt investigation for hyperparathyroidism, as early recognition of brown tumors allows appropriate systemic management and may lead to lesion regression after treatment of the endocrine disorder.
Bruno Teixeira Gonçalves Rodrigues, Vanessa Freitas Pacheco, Livia Xavier Costa do Rego Moreira, Mariana Cartaxo Faustini, Nathália de Almeida Freire, Danilo Passeado Branco Ribeiro, Mônica Simões Israel   +6 more
wiley   +1 more source

Rare Manifestation of Sjogren's Syndrome: Renal Tubular Acidosis‐Induced Hypokalemic Paralysis—A Case Report

Clinical Case Reports, Volume 14, Issue 5, May 2026.
ABSTRACT Sjogren's syndrome (SS) is an autoimmune disorder characterized by inflammation of exocrine glands, often presenting with symptoms such as dry eyes and mouth. Although less common, renal involvement can lead to serious complications like hypokalemic paralysis.
Premendra Vimal, Dhiraj Chaurasia, Dipesh Jha, Raj Adhikari   +3 more
wiley   +1 more source

Screening of hypercalciuria among children with persistent asymptomatic hematuria

Journal of Biostatistics and Epidemiology, 2018
Background & Aim: Hypercalciuria is commonly observed in accompany with some conditions. Hypercalciuria can clinically present different symptoms and signs. The diagnostic methods for hypercalciuria have not yet been standardized. The presented study was
Mohsen Akhavansepahi, Bibi Leila hoseini, Yaser Tabarai   +2 more
doaj  

a novel variant of gene in a neonate with congenital hypoparathyroidism [PDF]

Annals of Pediatric Endocrinology & Metabolism, 2018
Autosomal-dominant hypocalcemia with hypercalciuria (ADHH) is a genetic disease characterized by hypoparathyroidism with hypercalciuria. Most patients with ADHH have calcium-sensing receptor (CaSR) gene mutations.
Jung-Eun Moon, Su-Jeong Lee, Suk-Hyun Park, Jinsup Kim, Dong-Kyu Jin, Cheol Woo Ko   +5 more
doaj   +1 more source

The urinary calcium–magnesium product as a potential indicator of nephrolithiasis in primary hyperparathyroidism

Endokrynologia Polska
INTRODUCTION: Nephrolithiasis is a common complication of primary hyperparathyroidism (PHPT), but the mechanisms underlying stone formation remain incompletely understood.
Michał Popow, Sebastian Szewczyk, Janusz Sierdziński, Małgorzata Bobrowicz, Urszula Ambroziak   +4 more
doaj   +1 more source

Metabolic evaluation in patients with nephrolithiasis: A report from Isfahan, Iran

Advanced Biomedical Research, 2012
Background: Nephrolithiasis is a major public health problem worldwide. In recent years, growing evidence suggest that this disease may originate from underlying metabolic disorders.
Afsoon Emami-Naini, Amid Eshraghi, Shahrzad Shahidi, Mojgan Mortazavi, Shiva Seyrafian, Peyman Roomizadeh, Seyed-Hossein Abtahi, Hamed-Basir Ghafoori   +7 more
doaj   +1 more source

Carrier screening in the reproductive setting—Are there medical implications for the heterozygote?—A guide for clinicians

Pregnancy, Volume 2, Issue 3, May 2026.
Abstract Carrier screening for genetic conditions performed preconception or during pregnancy allows identification of fetal risk for inherited autosomal recessive and X‐linked conditions. The goal is to identify at‐risk patients/couples and offer them reproductive options such as preimplantation genetic diagnosis, prenatal testing, or targeted newborn
Emily B. Rosenfeld, Nicole Kasatkin, Bi Liu Yu, Milen Velinov, Justin S. Brandt, Elena Ashkinadze   +5 more
wiley   +1 more source

Opening closed inward rectifier potassium channel doors

British Journal of Pharmacology, Volume 183, Issue 10, Page 2197-2218, May 2026.
Inwardly rectifying potassium (KIR) channels are essential regulators of membrane potential in excitable and non‐excitable tissues. Although KIR channels exhibit a biophysical preference for potassium influx due to voltage‐dependent block of outward current by polyamines and Mg2+, under physiological conditions, they predominantly mediate K+ efflux ...
Anna Stary‐Weinzinger, Fabian Kaiser, Marcel A. G. van der Heyden, Saïd Bendahhou   +3 more
wiley   +1 more source

Primary Hyperparathyroidism in Adults: Recent Developments in Diagnosis and Management

Medical Journal of Australia, Volume 224, Issue 5, May 2026.
ABSTRACT Primary hyperparathyroidism has a prevalence of around 1% in the general population. Diagnosis requires biochemical testing of serum (for calcium and parathyroid hormone) and urine (for calcium excretion), as well as wider screening for complications including osteoporosis, renal disease, abdominal symptoms and neuropsychiatric disturbance. In
Elizabeth Wootton, Sunita M. C. De Sousa, Richard L. Prince, Donald S. A. McLeod, David A. Pattison, Mathis Grossmann   +5 more
wiley   +1 more source

Multisystem Sarcoidosis Presenting With Hypercalcemia, Lytic Bone Lesion, and Mesenteric Panniculitis in Chronic Kidney Disease

Clinical Case Reports, Volume 14, Issue 4, April 2026.
The clinical photograph shows bilateral leg swelling with right‐sided predominance and cutaneous changes. CT images (A–C) demonstrate abdominal and retroperitoneal lymphadenopathy, and image D shows a hypodense lytic spinal lesion, suggesting multifocal disease involving the abdomen, retroperitoneum, and spine.
Aishwarya Holi, Karuna Rayamajhi, Satya Rijal, Niket Shah, Aaron Sousa, Gina Chacon Osorio   +5 more
wiley   +1 more source