Search Results - "HYPERCALCIUREA"

Association of demographic and biochemical factors with hypercalciuria among Meitei adults in Manipur, Northeast India: a cross-sectional study.

Authors: Aheibam, Robertson Singh Yumnam, Malvika Pebam, Erika et al.

Source: Osong Public Health & Research Perspectives. Oct2025, Vol. 16 Issue 5, p519-529. 11p.

Subject Terms: Risk assessment, Cross-sectional method, Predictive tests, Hypercalciurea, Creatinine, Data analysis, Receiver operating characteristic curves, Research funding, Statistical sampling, Multiple regression analysis, Kidney stones, Disease prevalence, Chi-squared test, Descriptive statistics, Age distribution, Calcium, One-way analysis of variance, Statistics, Sociodemographic factors, Data analysis software, Confidence intervals, Disease incidence, Biomarkers, Disease risk factors, Adults

Geographic Terms: India

Fanconi-Bickel syndrome complicated by nephrocalcinosis and GFR decline.

Authors: Baqai, Kanza Bassetti, Jennifer A. Kovanlikaya, Arzu et al.

Source: Pediatric Nephrology. Nov2024, Vol. 39 Issue 11, p3201-3204. 4p.

Subject Terms: *BIOPSY, *HYPERCALCIUREA, *CHRONIC kidney failure, *FANCONI syndrome, *GLYCOGEN, *KIDNEY calcification, *LIVER, *PATIENT monitoring, *GLOMERULAR filtration rate, *KIDNEYS, *HYPOPHOSPHATEMIA, *GENETIC testing, *DISEASE risk factors, *DISEASE complications

Novel Variant of SLC34A3 in a Compound Heterozygous Brazilian Girl with Hereditary Hypophosphatemic Rickets with Hypercalciuria.

Authors: Pinto Valadares, Luciana Rocha de Carvalho, Daniel

Source: Journal of Clinical Research in Pediatric Endocrinology; Sep2025, Vol. 17 Issue 3, p326-331, 6p

Subject Terms: KNEE pain, BLOOD gases analysis, OSTEOPENIA, RISK assessment, HYPERCALCIUREA, CARRIER proteins, SKELETAL muscle, BONE diseases, RICKETS, ANTIHYPERTENSIVE agents, DIURETICS, ROUTINE diagnostic tests, CALCITRIOL, CHRONIC kidney failure, URINALYSIS, GENETIC mutation, HYPOPHOSPHATEMIA, GENETIC testing, DISEASE risk factors, DISEASE complications

Geographic Terms: BRAZIL

Hipomagnesemia familiar con hipercalciuria y nefrocalcinosis por mutación del gen CLDN16 (Claudina 16). Reporte de caso.

Alternate Title: Familial hypomagnesemia with hypercalciuria and nefrocalcinosis due to a mutation in the CLDN16 gen (Claudina 16). A case report.

Authors: Munarriz, Reyner Loza Cáceres, Fernando Arias Chagua, Víctor Neyra

Source: Revista Medica Herediana. jul-sep2024, Vol. 35 Issue 3, p157-161. 5p.

Subject Terms: *KIDNEY transplantation, *HYPERCALCIUREA, *MAGNESIUM, *GRAFT survival, *CHRONIC kidney failure, *SURGICAL complications, *HYPOCALCEMIA, *HYPOMAGNESEMIA, *KIDNEY calcification, *GENETIC mutation, *HYPERMAGNESEMIA, *GENETIC testing

Unexpected SLC34A3 rickets in a case of suspected distal myopathy.

Authors: Sharova, Margarita Subbotin, Dmitrii Murtazina, Aysylu et al.

Source: Pediatric Nephrology; Dec2025, Vol. 40 Issue 12, p3647-3649, 3p

Subject Terms: RICKETS treatment, RISK assessment, PHYSICAL diagnosis, HYPERCALCIUREA, DIFFERENTIAL diagnosis, CARRIER proteins, MUSCLE diseases, RICKETS, GENETIC counseling, CHRONIC kidney failure, X-rays, GENETIC mutation, SEQUENCE analysis, GENOMES, HYPOPHOSPHATEMIA, PHENOTYPES, DISEASE risk factors, DISEASE complications, SYMPTOMS

A Rare Cause of Hypergonadotropic Hypogonadism: Transaldolase Deficiency in Two Siblings.

Authors: Yıldız, Melek Önal, Zerrin Yeşil, Gözde et al.

Source: Journal of Clinical Research in Pediatric Endocrinology; Mar2025, Vol. 17 Issue 1, p97-102, 6p

Subject Terms: INBORN errors of metabolism diagnosis, PHYSICAL diagnosis, CONGENITAL heart disease, PROTEINURIA, CIRRHOSIS of the liver, CYTOPENIA, HYPERCALCIUREA, DIFFERENTIAL diagnosis, RARE diseases, CHRONIC kidney failure, HYPOGONADISM, TRANSFERASES, GENETIC mutation, CRYPTORCHISM, EARLY diagnosis, SEQUENCE analysis

Acute Encephalopathy and Refractory Hypokalemia in a 12-Year-Old Boy.

Authors: Moosavian, Toktam Pournasiri, Zahra Fatollahierad, Shiva

Source: Iranian Journal of Child Neurology. Winter2025, Vol. 19 Issue 1, p107-112. 6p.

Subject Terms: Hepatolenticular degeneration diagnosis, Copper metabolism, Therapeutic use of ubiquinones, Therapeutic use of folic acid, Cerebrospinal fluid examination, Neurologic examination, Biotin, Hypercalciurea, Blood proteins, Copper, Brain, Brain diseases, Fever, Globulins, Zinc compounds, Vitamin B complex, Magnetic resonance imaging, Hypokalemia, Creatine kinase, Hepatolenticular degeneration, Cell death, Lactates, Urinalysis, Genetic mutation, Liver, Biomarkers, Anticonvulsants, Symptoms, Children

Pediatric Urinary Stone Disease: A 10-Year Single-Center Experience from Türkiye.

Authors: Dönger, Utku İncekaş, Caner Gülleroğlu, Kaan Savaş et al.

Source: Turkish Archives of Pediatrics; Jan2025, Vol. 60 Issue 1, p29-33, 5p

Subject Terms: METABOLIC disorders, URINARY tract infections, HYPERCALCIUREA, URINARY calculi, CONSANGUINITY, RETROSPECTIVE studies, FAMILY history (Medicine), DESCRIPTIVE statistics, MANN Whitney U Test, MEDICAL records, ACQUISITION of data, CITRATES, DATA analysis software, DISEASE risk factors, SYMPTOMS, CHILDREN

Geographic Terms: TURKEY

Effects of SLC34A3 or SLC34A1 variants on calcium and phosphorus homeostasis.

Authors: Naciri Bennani, Hamza Chtioui, Imane Allirot, Camille et al.

Source: Pediatric Nephrology; Jan2025, Vol. 40 Issue 1, p117-129, 13p

Subject Terms: KIDNEY stone risk factors, PHOSPHORUS metabolism, CALCIUM metabolism, RISK assessment, FLUCONAZOLE, HOMEOSTASIS, CARRIER proteins, ACADEMIC medical centers, HYPERCALCIUREA, HYPERCHOLESTEREMIA, GENOMICS, FLUID therapy, RETROSPECTIVE studies, CHILDREN'S hospitals, DNA, DESCRIPTIVE statistics, QUANTITATIVE research, GENES, GENETIC polymorphisms, MEDICAL records, ACQUISITION of data, KIDNEY calcification, COMPARATIVE studies, DATA analysis software, CASE studies, COLIC, DIET, SEQUENCE analysis, HYPOPHOSPHATEMIA, DISEASE risk factors, CHILDREN

Geographic Terms: FRANCE

Infantile nephrocalcinosis with chronic diarrhea.

Authors: Rahman, Rehna K. Raghavan, Vinitha Vijaya Pachat, Divya

Source: Pediatric Nephrology; Apr2025, Vol. 40 Issue 4, p951-953, 3p

Subject Terms: FECAL analysis, PHYSICAL diagnosis, HYPERCALCIUREA, LACTOSE intolerance, POTASSIUM compounds, DIARRHEA in children, GENE expression profiling, KIDNEY calcification, GENETIC mutation, DIET therapy, DIET in disease, SEQUENCE analysis, PHENOTYPES

Molecular Aspects of Distal Kidney Tubular Acidosis in Children, Its Long-Term Outcome, and Relationship with Hyperammonemia.

Authors: Güven, Serçin Gökçe, İbrahim Alavanda, Ceren et al.

Source: Turkish Archives of Pediatrics. Jul2022, Vol. 57 Issue 4, p432-440. 9p.

Subject Terms: *KIDNEY physiology, *HYPERCALCIUREA, *SENSORINEURAL hearing loss, *SYMPTOMS, *GENES, *GENETIC mutation, *KIDNEY calcification, *ACIDOSIS, *GENETICS, *GLOMERULAR filtration rate

Bones, Stones, and Hematuria - Connecting the Dots.

Authors: Fadnis, Madhura P. Kalrao, Vijay Kalra, Suprita et al.

Source: Indian Journal of Nephrology; Mar/Apr2025, Vol. 35 Issue 2, p1-3, 3p

Subject Terms: KIDNEY stones diagnosis, KIDNEY function tests, HYPERCALCIUREA, BODY weight, URINARY organs, HEMATURIA, RICKETS, FAMILY history (Medicine), HYPOCALCEMIA, STATURE, GENE expression, POLYURIA, CHILD development, GROWTH disorders, HYPOMAGNESEMIA, KIDNEY calcification, GENETIC mutation, KIDNEYS, SEQUENCE analysis, GENETICS

Jaw bone changes in panoramic radiography in patients with hyperparathyroidism.

Authors: Mohammadi, Maryam Alinejad, Saeed Abesi, Farida

Source: Journal of Shahrekord University of Medical Sciences; Sep2024, Vol. 26 Issue 3, p101-107, 7p

Subject Terms: RADIOGRAPHY, HYPERPARATHYROIDISM, ENDOCRINE diseases, HYPERCALCIUREA, CALCIUM metabolism disorders

A previously healthy 3-year-old female with hypertension, proteinuria, and hypercalciuria.

Authors: Liu, Tao Wang, Wenhong Liu, Zhufeng et al.

Source: Pediatric Nephrology; Apr2024, Vol. 39 Issue 4, p1301-1313, 13p

Subject Terms: TREATMENT of rare diseases, CRANIAL radiography, HYPERTENSION, MAGNETIC resonance angiography, ECHOCARDIOGRAPHY, GENETIC mutation, GENETIC testing, PROTEINURIA, COMPUTED tomography, HYPERCALCIUREA, RARE diseases

Treatment of paediatric renal tubular acidosis with a prolonged-release alkali supplementation.

Authors: Tan, Hai Liang Marlais, Matko Veligratli, Faidra et al.

Source: Pediatric Nephrology; Nov2024, Vol. 39 Issue 11, p3373-3375, 3p

Subject Terms: RENAL tubular transport disorders, CONTROLLED release preparations, KIDNEY tubules, HYPERCALCIUREA, INBORN errors of metabolism, URINARY calculi, TREATMENT effectiveness, RICKETS, ALKALIES, CHRONIC diseases, DRUG efficacy, KIDNEY calcification, HYPOALDOSTERONISM, DIETARY supplements, ACIDOSIS, OSTEOMALACIA, CHILDREN

Urinary excretion of calcium, phosphate, magnesium, and uric acid in healthy infants and young children. Influence of feeding practices in early infancy.

Authors: Peris Vidal, Amelia Ferrando Monleón, Susana Marín Serra, Juan et al.

Source: Pediatric Nephrology; Mar2024, Vol. 39 Issue 3, p761-770, 10p

Subject Terms: BREASTFEEDING techniques, REFERENCE values, STATISTICS, ANALYSIS of variance, SOFTWARE architecture, MAGNESIUM, DESCRIPTIVE statistics, CALCIUM, DIETARY calcium, URIC acid, STATISTICAL models, DATA analysis, HYPERCALCIUREA, CREATININE, PHOSPHATES, CHILDREN

Geographic Terms: SPAIN

Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis (FHHNC): A Cross-sectional Study from Malaysia.

Authors: Bee Shuang Lee Suet Li Yap Jia Ni Lee

Source: Asian Journal of Pediatric Nephrology; Jan-Jun2024, Vol. 7 Issue 1, p3-6, 4p

Subject Terms: CROSS-sectional method, PUBLIC hospitals, HYPERCALCIUREA, EARLY medical intervention, SCIENTIFIC observation, EYE abnormalities, RETROSPECTIVE studies, DESCRIPTIVE statistics, PEDIATRICS, GENETIC disorders, HYPOMAGNESEMIA, KIDNEY calcification, GENETIC mutation, KIDNEY diseases, EARLY diagnosis, PHENOTYPES, GENOTYPES, MEMBRANE proteins, DISEASE progression, GENETIC testing

Geographic Terms: MALAYSIA

Type 1 Renal Tubular Acidosis in Wilson's Disease.

Authors: Swain, Abinash Bhoi, Sanjeev Kumar Jha, Menka et al.

Source: Annals of Indian Academy of Neurology; Jul/Aug2024, Vol. 27 Issue 4, p460-462, 3p

Subject Terms: COPPER analysis, BLOOD gases analysis, HYPERCALCIUREA, RESEARCH funding, URINARY calculi, AMMONIUM chloride, DESCRIPTIVE statistics, MAGNETIC resonance imaging, HEPATOLENTICULAR degeneration, RENAL osteodystrophy, MEDICAL screening, EARLY diagnosis, ACIDOSIS, SYMPTOMS

Association between the metabolic profile of urolithiasis in children with idiopathic hypercalciuria and the composition of the stone assessed by infrared spectroscopy.

Authors: Placzyńska, Małgorzata Milart, Joanna Lubas, Arkadiusz et al.

Source: Polish Journal of Pediatrics / Pediatria Polska; 2023, Vol. 98 Issue 4, p271-277, 7p

Subject Terms: PHOSPHORUS analysis, STATISTICS, NEAR infrared spectroscopy, HYDROGEN-ion concentration, MANN Whitney U Test, T-test (Statistics), PEARSON correlation (Statistics), MAGNESIUM, DESCRIPTIVE statistics, URINALYSIS, CALCIUM, OXALIC acid, ACYCLIC acids, LOGISTIC regression analysis, RECEIVER operating characteristic curves, DATA analysis software, URINARY calculi, HYPERCALCIUREA, CHILDREN

İzole persistan proteinüri ile başvuran bir olguda Tip 1 Dent hastalığı.

Alternate Title: A case of Type 1 Dent disease presenting with isolated persistant proteinuria.

Authors: Güngör, Tülin Eroğlu, Fehime Kara Yazılıtaş, Fatma et al.

Source: Türk Pediatri Arşivi. 2020, Vol. 55 Issue 1, p72-75. 4p.

Subject Terms: *DIFFERENTIAL diagnosis, *HYPERCALCIUREA, *X-linked genetic disorders, *GENETIC mutation, *PROTEINURIA