Search results for "hyperparathyroidism"

showing 10 items of 57 documents

Short Ammonium Chloride Loading Test for Evaluation of Hyperparathyroidism

1981

The dilemma in the diagnosis of hyperparathyroidism (HPT) is reflected by three factors: Hypercalcemia is still regarded as the most important diagnostic sign, but unless multiple determinations of serum calcium are done, the so-called borderline cases will be missed. Tests that readily identify HPT combine either simple performance, widespread use and low accuracy (CP, TRP, PEI, TMP/GFR)l or sophisticated methods, limited use and high accuracy (PTH, Ca+++, c-AMP). Consequently, some authors perform neck explorations to cure patients with recurrent nephrolithiasis who do not fulfill the diagnostic criteria of HPT. However, the stone recurrence rate may then reach 75%2,3 In this situation, t…

Ammonium chloride loading testHyperparathyroidismmedicine.medical_specialtyStone patientNeck explorationbusiness.industrymedicineUrologymedicine.diseasebusinessParathyroid adenoma
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Management of secondary hyperparathyroidism in uremic patients : the role of the new vitamin D analogs

2007

Secondary hyperparathyroidism - a common comorbid condition in patients with chronic renal insufficiency - is considered a consequence of critical determinants such as hypocalcemia, phosphate retention and reduced levels of calcitriol production. In this complex mechanism, the skeletal apparatus and the nonskeletal targets such as vascular and heart valves are often involved, thus explaining the increased risk of cardiovascular morbidity and mortality of uremic patients. In this review we will focus on the major role played by Calcitriol deficiency as a trigger of secondary hyperparathyroidism and the crucial need for obiquitous vitamin D receptor activation in order to have an optimal PTH …

Bone Density Conservation AgentsCalcitriolHypocalcemiaErgocalciferolsHumansReceptors CalcitriolHyperparathyroidism SecondaryRenal Insufficiency ChronicVitamin DVitamin D DeficiencyPhosphatesUremia
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Osteoporosis, densidad mineral ósea y complejo CKD-MBD (I): consideraciones diagnósticas

2018

Resumen: Osteoporosis (OP) y enfermedad renal crónica (ERC) influyen de manera independiente en la salud ósea y cardiovascular. Un número significativo de pacientes con ERC, especialmente desde estadios 3a a 5D, presentan una disminución significativa de la densidad mineral ósea condicionando un alto riesgo de fractura y un incremento importante de la morbimortalidad asociada. Independientemente de la OP clásica asociada a edad y/o sexo, las propiedades mecánicas del hueso se encuentran afectadas adicionalmente por factores intrínsecos a la ERC («OP urémica»). En la primera parte de esta revisión, analizaremos conceptos generales sobre densidad mineral ósea, OP y fracturas, en gran parte in…

Bone mineralmedicine.medical_specialtyHyperparathyroidismSenile osteoporosisbusiness.industryOsteoporosis030232 urology & nephrology030209 endocrinology & metabolismContext (language use)lcsh:Diseases of the genitourinary system. Urologylcsh:RC870-923urologic and male genital diseasesmedicine.diseaseLower riskfemale genital diseases and pregnancy complications03 medical and health sciences0302 clinical medicineNephrologyInherent riskInternal medicinemedicinebusinessKidney diseaseNefrología
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Dissimilar PTH, Gastrin, and Calcitonin Responses to Oral Calcium and Peptones in Hypocalciuric Hypercalcemia, Primary Hyperparathyroidism, and Norma…

2005

We analyzed gastrin, PTH, and calcitonin responses to oral calcium and peptones in hypocalciuric hypercalcemia, mild primary hyperparathyroidism, and normal controls. We observed diverse hormonal responses that may help in the differential diagnosis of these conditions. Introduction: Hypocalciuric hypercalcemia (HH) is consequent to calcium-sensing receptor (CaSR) genetic mutations or anti-CaSR antibodies. CaSR is expressed in parathyroid tissue, thyroid C cells, and gastrin-secreting cells, where it has been suggested that on calcium and/or amino acid allosteric activation, promotes gastrin secretion. Materials and Methods: We evaluated gastrin, PTH, and calcitonin responses to oral calciu…

CalcitoninMalemedicine.medical_specialtyPeptide HormonesEndocrinology Diabetes and Metabolismchemistry.chemical_elementParathyroid hormoneCalciumDiagnosis DifferentialInternal medicineGastrinsmedicineHumansOrthopedics and Sports MedicineAgedGastrinHyperparathyroidismHypocalcemiaFamilial hypocalciuric hypercalcemiabusiness.industryHyperparathyroidismMiddle Agedmedicine.diseaseEndocrinologychemistryParathyroid HormoneCalcitoninPeptonesCalciumFemaleCalcium-sensing receptorbusinesshormones hormone substitutes and hormone antagonistsPrimary hyperparathyroidismJournal of Bone and Mineral Research
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Mandibular brown tumor as the first manifestation of primary hyperparathyroidism: a case report

2013

Case ReportMandibular brown tumor primary hyperparathyroidism
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SP619The effect of etelcalcetide in hemodialysis patients with secondary hyperparathyroidism in daily clinical practice. A prospective multicenter st…

2019

EtelcalcetideTransplantationPediatricsmedicine.medical_specialtybusiness.industrymedicine.medical_treatmentmedicine.diseaseClinical PracticeMulticenter studyNephrologymedicineSecondary hyperparathyroidismHemodialysisbusinessNephrology Dialysis Transplantation
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Lebensqualität nach operativer Therapie des renalen Hyperparathyreoidismus. Ergebnisse einer prospektiven Langzeitstudie / Quality of Life After Oper…

2001

In einer prospektiven Langzeituntersuchung wurde die Lebensqualitat nach operativer Therapie des renalen Hyperparathyreoidismus untersucht. Vom 1.8.1987-31.8.2000 erfolgten 186 Eingriffe. Bevorzugte Operation war die totale Parathyreoidektomie mit autologer Epithelkorperchenreplantation. Die Erfolgsrate der erstmaligen Halsexploration betrug 98,2%. Juckreiz klang bei uber 60% der betroffenen Patienten innerhalb von 4 Wochen nach dem Eingriff ab. Die Ruckbildung ossarer Symptome bedurfte langerer Zeit. Ein Jahr postoperativ waren 75% der praoperativ von Juckreiz und 79% der vom ossaren Syndrom betroffenen Patienten asymptomatisch. Patienteneigene Risikofaktoren bedingen eine niedrige Letalit…

Gynecologymedicine.medical_specialtyRenal hyperparathyroidismQuality of lifebusiness.industryLong term follow upMedicineOperative therapybusiness
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Parathyroid hormone and insulin-resistance in essential hypertension

2000

Hyperparathyroidismmedicine.medical_specialtybusiness.industryInsulinmedicine.medical_treatmentParathyroid hormonemedicine.diseaseEssential hypertensionEndocrinologyBlood pressureInsulin resistanceInternal medicineDiabetes mellitusInternal MedicinemedicineSystolebusinessAmerican Journal of Hypertension
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Risk Profiles and Penetrance Estimations in Multiple Endocrine Neoplasia Type 2A Caused by Germline RET Mutations Located in Exon 10

2010

Multiple endocrine neoplasia type 2 is characterized by germline mutations in RET. For exon 10, comprehensive molecular and corresponding phenotypic data are scarce. The International RET Exon 10 Consortium, comprising 27 centers from 15 countries, analyzed patients with RET exon 10 mutations for clinical-risk profiles. Presentation, age-dependent penetrance, and stage at presentation of medullary thyroid carcinoma (MTC), pheochromocytoma, and hyperparathyroidism were studied. A total of 340 subjects from 103 families, age 4-86, were registered. There were 21 distinct single nucleotide germline mutations located in codons 609 (45 subjects), 611 (50), 618 (94), and 620 (151). MTC was present…

MalePHEOCHROMOCYTOMAendocrine system diseasesMEDULLARY-THYROID CARCINOMAAdrenal Gland NeoplasmsMultiple Endocrine Neoplasia Type 2aPenetrancemedicine.disease_causePHENOTYPEGermlineExon0302 clinical medicinemedullary thyroid carcinomaMEN2BMEN2AChildGenetics (clinical)GeneticsAged 80 and overMutationHyperparathyroidismLife SciencesExonsMiddle AgedCARRIERSPenetranceCANCERPROPHYLACTIC THYROIDECTOMY3. Good healthgenotype-phenotypeFAMILYMEN2030220 oncology & carcinogenesisChild PreschoolFemaleAdultAdolescent030209 endocrinology & metabolismMultiple endocrine neoplasia type 2BiologyPheochromocytoma03 medical and health sciencesYoung AdultGermline mutationGeneticsmedicineHumansThyroid NeoplasmsCodonGerm-Line MutationAgedNeoplasm StagingProto-Oncogene Proteins c-retCancerHIRSCHSPRUNG-DISEASEPROTOONCOGENEmedicine.diseaseGENECarcinoma NeuroendocrineCancer researchRETHuman Mutation
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Blueberry Muffin Baby Associated with Bone Demineralization Due to Congenital Transient Neonatal Hyperparathyroidism

2014

MalePediatricsmedicine.medical_specialtybusiness.industryHyperparathyroidismRemission SpontaneousInfant NewbornGestational AgeDermatologyBlueberry muffin babySkin DiseasesThrombocytopeniaSurgeryDemineralizationHematopoiesis ExtramedullaryPediatrics Perinatology and Child HealthmedicineTransient Neonatal HyperparathyroidismHumansmedicine.symptombusinessBone Demineralization PathologicInfant PrematurePediatric Dermatology
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