Search results for "Osteodystrophy"

showing 6 items of 6 documents

Bone Resorption in Kidney Transplant Recipients

2009

Early diagnosis of persistent hyperparathyroidism (HP) following kidney transplantation may prevent worsening of osteodystrophy and potential damage to the graft. We evaluated the utility of collagen pyridinoline (PYD) and deoxypyridinoline (DPD) urinary cross-links beyond the common HP markers to evaluate 70 selected stable recipients between 1997 and 2006 who were divided into 2 group depending on the immunosuppressive protocol. All patients showed elevated levels of urinary cross-links even though calcemia and phosphoremia values were normal. Their mean creatinine level was slightly increased. Data were assessed as mean values +/- SD. All variables underwent a correlation matrix analysis…

AdultMalemedicine.medical_specialtyDeoxypyridinolineUrologyCollagen Type IBone resorptionBone remodelingchemistry.chemical_compoundInternal medicinemedicineHumansOsteodystrophyAmino AcidsBone ResorptionAgedTransplantationCreatinineHyperparathyroidismPyridinolinebusiness.industryHyperparathyroidismhyperparathyroidism kidney transplantation urinary cross-linksMiddle AgedAlkaline Phosphatasemedicine.diseaseKidney TransplantationTransplant RecipientsTransplantationSettore MED/18 - Chirurgia GeneraleEndocrinologychemistryCreatinineFemaleSurgerybusinessBiomarkersTransplantation Proceedings
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The treatment of wrist fractures with Epibloc System

2011

BACKGROUND Fractures of the distal extremity of the radius are the most common bone lesions of the superior extremity of the body, representing 17% of the fractures treated in First Aid facilities. The restoration of anatomical relationships in the radiocarpal joint is considered to be a prerequisite for good functional recovery. There are numerous methods of treatment of these fractures. The Epibloc system is a percutaneous endomedullary synthesis alternative to the plaster cast in wrist fracture treatment. MATERIALS AND METHODS The authors describe their experience with 81 fractures (63 type A2-3 fractures and 18 type C1) of the wrist treated with the Epibloc System (ES). The results were…

AdultMalemedicine.medical_specialtyPercutaneousmedicine.medical_treatmentWristBone NailsFracture Fixation InternalFractures BoneMedicineHumansOrthopedics and Sports MedicineOsteodystrophyMalunionReduction (orthopedic surgery)Agedbusiness.industryRehabilitationMiddle Agedmedicine.diseaseFunctional recoveryWrist InjuriesSurgeryPercutaneous pinningmedicine.anatomical_structureTreatment Outcomedistal radius fracture wrist fracture Epibloc system percutaneous synthesis percutaneous pinningFemaleWRIST FRACTUREbusiness
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A new heterozygous mutation (L338N) in the human Gsalpha (GNAS1) gene as a cause for congenital hypothyroidism in Albright's hereditary osteodystroph…

2003

OBJECTIVE: To identify the molecular defect by which psychomotor retardation is caused in two brothers with congenital hypothyroidism who received adequate treatment with l-thyroxine. CASE REPORT: A six-year-old boy presented with psychomotor retardation and congenital primary hypothyroidism (CH). The patient had a normal blood thyrotrophin (TSH) level on neonatal screening, but low total serum thyroxine and triiodothyronine concentrations prompting thyroid hormone substitution shortly after birth. Nevertheless, psychomotor development was retarded and the patient underwent further investigation. Typical features of Albright's hereditary osteodystrophy (AHO) such as round face, obesity, and…

Malemedicine.medical_specialtyHeterozygoteGenotypeEndocrinology Diabetes and MetabolismThyrotropinFibrous Dysplasia PolyostoticEndocrinologyHypothyroidismInternal medicinemedicineGTP-Binding Protein alpha Subunits GsHumansOsteodystrophyChildAlbright's hereditary osteodystrophyPseudohypoparathyroidismPsychomotor retardationbusiness.industryThyroidErythrocyte MembranePrimary hypothyroidismGeneral MedicineSequence Analysis DNAmedicine.diseaseCongenital hypothyroidismPedigreeThyroxineEndocrinologymedicine.anatomical_structureMutationTriiodothyroninePseudopseudohypoparathyroidismCalciummedicine.symptomMetacarpusPsychomotor DisordersbusinessEuropean journal of endocrinology
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Evolution of otosclerosis to cochlear implantation.

2011

Abstract Introduction Otosclerosis is an osteodystrophy of the labyrinthine capsule producing conductive hearing loss. If the process invades the cochlea, a sensorineural hearing loss usually takes place. The cochlear implant is a good alternative in these patients. Objective To ascertain the behaviour of cochlear implantation (CI) in otosclerosis. Material and methods We reviewed a database of 250 patients who underwent CI, performing a retrospective study of 13 patients with clinical, audiological and/or imaging findings of bilateral otosclerosis. The 26 ears were studied as to their natural history, previous surgeries, evolution to profound hearing loss, computed tomography (CT) images, …

Malemedicine.medical_specialtymedicine.medical_treatmentHearing Loss SensorineuralHearing Loss ConductiveDentistryStapes SurgeryHearing Loss BilateralTinnitusCochlear implantotorhinolaryngologic diseasesmedicineHumansOsteodystrophyAgedRetrospective Studiesbusiness.industryImplant failureRetrospective cohort studyGeneral MedicineMiddle Agedmedicine.diseaseFacial nerveSurgeryConductive hearing lossFacial NerveCochlear ImplantsOtosclerosisTreatment OutcomeDisease ProgressionOtosclerosisSensorineural hearing lossFemalebusinessTomography X-Ray ComputedActa otorrinolaringologica espanola
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Osteodystrophy in chronic liver diseases

2013

Osteoporosis and osteomalacia are, to date, among the most common metabolic diseases in the world. Lately, an association between metabolic bone diseases and chronic liver disease has been increasingly reported, inducing many authors to create a new nosographic entity known as 'hepatic osteodystrophy.' The importance of such a condition is further increased by the morbidity of these two diseases, which greatly reduce the quality of life because of frequent fractures, especially vertebral and femoral neck ones. For this reason, early identification of high-risk patients should be routinely performed by measuring bone mass density. The explanation for the association between bone diseases and…

Pediatricsmedicine.medical_specialtyPathologySettore MED/09 - Medicina InternaOsteoporosisInterferon therapychronic liver diseasesChronic liver diseaseBone DensityRisk FactorsInternal MedicinemedicineHumansOsteodystrophyFrequent fracturesFemoral neckOsteomalaciaDiphosphonatesbusiness.industryLiver Diseasesmedicine.diseaseOsteodystrophyBone Diseases Metabolicmedicine.anatomical_structureChronic DiseaseOsteomalaciaQuality of LifeEmergency MedicineBone mass densityOsteoporosisOsteodystrophy; chronic liver diseasesbusinessInternal and Emergency Medicine
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Osteoporosis, densidad mineral ósea y complejo CKD-MBD (II): implicaciones terapéuticas

2019

Resumen: La osteoporosis (OP) y la enfermedad renal crónica (ERC) influyen independientemente en la salud ósea. Numerosos pacientes con ERC presentan una disminución de densidad mineral ósea (DMO), un elevado riesgo de fracturas por fragilidad ósea y un incremento de su morbimortalidad. Con el envejecimiento de la población estos hechos no son dependientes solo de la «osteodistrofia renal» sino también de la OP asociada. Dado que la DMO tiene capacidad predictiva en pacientes con ERC (parte I), ahora analizaremos las implicaciones terapéuticas derivadas. Análisis post hoc de estudios aleatorizados han mostrado que fármacos como alendronato, risedronato, raloxifeno, teriparatida o denosumab …

medicine.medical_specialtyeducation.field_of_studyHyperparathyroidismbusiness.industryPopulationOsteoporosis030232 urology & nephrologyurologic and male genital diseasesmedicine.diseaselcsh:Diseases of the genitourinary system. Urologylcsh:RC870-92303 medical and health sciences0302 clinical medicineDenosumabNephrologyInternal medicinemedicineTeriparatideRaloxifeneRenal osteodystrophy030212 general & internal medicinebusinesseducationmedicine.drugKidney diseaseNefrología
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