Search results for "Dystrophy"

showing 10 items of 268 documents

Franceschetti Hereditary Recurrent Corneal Erosion

2011

To describe new affected individuals of Franceschetti's original pedigree of hereditary recurrent erosion and to classify a unique entity called Franceschetti corneal dystrophy.Observational case series.Slit-lamp examination of 10 affected individuals was conducted. Biomicroscopic examinations were supplemented by peripheral corneal biopsy in 1 affected patient with corneal haze. Tissue was processed for light and electron microscopy and immunohistochemistry was performed. DNA analysis was carried out in 12 affected and 3 nonaffected family members.All affected individuals suffered from severe ocular pain in the first decade of life, attributable to recurrent corneal erosions. Six adult pat…

AdultMalemedicine.medical_specialtyBiopsyDNA Mutational AnalysisDermatan SulfateCorneal dystrophyCorneal OpacityCorneal erosionAntigens NeoplasmRecurrenceTransforming Growth Factor betaOphthalmologymedicineEye PainHumansChildAgedAged 80 and overCorneal Dystrophies HereditaryExtracellular Matrix Proteinsbusiness.industryCadherinsmedicine.diseaseImmunohistochemistryPedigreeRecurrent corneal erosionOphthalmologyClaudinsFemaleDecorinbusinessCell Adhesion MoleculesChondroitinBiomarkersAmerican Journal of Ophthalmology
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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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Lack of genetic association of neutral endopeptidase (NEP) with complex regional pain syndrome (CRPS)

2010

Complex regional pain syndrome (CRPS) is a condition that is characterized by severe pain and exaggerated neurogenic inflammation, which may develop after injury or surgery. Neurogenic inflammation is mediated by neuropeptides, such as calcitonin gene-related peptide (CGRP) and substance P (SP) that are released from nociceptors. Genetic factors may play a role in CRPS as was suggested by the occurrence of familial cases and several genetic association studies investigating mainly the human leukocyte antigen (HLA) system. Here we investigated the role of neutral endopeptidase (NEP), a key enzyme in neuropeptide catabolism. NEP dysfunction resulting in reduced inactivation of neuropeptides m…

AdultMalemedicine.medical_specialtyLinkage disequilibrium5' Flanking RegionSubstance PHuman leukocyte antigenBiologyCalcitonin gene-related peptideLinkage Disequilibriumchemistry.chemical_compoundInternal medicinemedicineHumansGenetic Predisposition to DiseaseDinucleotide RepeatsPromoter Regions GeneticNeprilysinGenetic Association StudiesGenetic associationNeurogenic inflammationPolymorphism GeneticGeneral NeurosciencefungiMiddle Agedmedicine.diseaseCRPS Pain NEP Association reflex sympathetic dystrophy syndrome type-i facilitated neurogenic inflammation nociceptive abnormalities alzheimers-disease neprilysin gene rat model enkephalinase prevalence dystoniaEndocrinologyComplex regional pain syndromechemistryCase-Control StudiesFemaleNeprilysinComplex Regional Pain Syndromes
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Relapsing and Progressive Complications of Severe Hypertriglyceridemia: Effective Long-Term Treatment with Double Filtration Plasmapheresis

2019

<b><i>Background:</i></b> Severe hypertriglyceridemia (HTG) is associated with major complications such as acute or relapsing pancreatitis (AP) and atherosclerotic cardiovascular disease (ASCVD). Rapid elimination of triglyceride (TG)-rich lipoproteins (LP) with double filtration plasmapheresis (DFPP) without need for substitution has been found to be effective for the acute, short-term treatment of HTG-induced AP. Data on the long-term use of DFPP to prevent HTG-associated complications are scarce. <b><i>Objectives:</i></b> To evaluate the use and efficacy of regular DFPP treatment in clinical practice for preventing recurrence of HTG-associa…

AdultMalemedicine.medical_specialtyMedizin030232 urology & nephrology030204 cardiovascular system & hematologySeverity of Illness IndexGastroenterology03 medical and health sciences0302 clinical medicinePharmacotherapyRefractoryRecurrenceInterquartile rangeInternal medicinemedicineHumansRetrospective StudiesHypertriglyceridemiaPregnancybusiness.industryHypertriglyceridemiaPlasmapheresisHematologyGeneral MedicineMiddle Agedmedicine.disease3. Good healthTreatment OutcomeNephrologyDisease ProgressionAcute pancreatitisFemaleLipodystrophybusinessComplicationBlood Purification
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Phosphomannosyl receptors of lysosomal enzymes of skeletal muscle in neuromuscular diseases.

1988

The phosphomannosyl receptor system is responsible for both the receptor-mediated endocytosis and the intracellular transport of lysosomal enzymes. In the present study this receptor system was examined in affected muscles of patients with various neuromuscular diseases. The total activity of beta-N-acetyl-glucosaminidase, a marker enzyme of lysosomal hydrolases, was significantly elevated in the patients with myopathies (polymyositis and muscular dystrophies) but only slightly increased in those with neurogenic muscle atrophies (amyotrophic lateral sclerosis, polyneuropathy or other neurogenic muscle disease). The increase was most prominent in the group of polymyositis. The content of pho…

AdultMalemedicine.medical_specialtyNeuromuscular diseaseAdolescentReceptors Cytoplasmic and NuclearReceptors Cell SurfaceBiologyPolymyositisReceptor IGF Type 2Internal medicineLysosomemedicineHumansAmyotrophic lateral sclerosisMuscular dystrophyReceptorAgedMusclesSkeletal muscleGeneral MedicineNeuromuscular DiseasesMiddle Agedmedicine.diseaseMuscle atrophymedicine.anatomical_structureEndocrinologyNeurologyFemaleNeurology (clinical)medicine.symptomLysosomesActa neurologica Scandinavica
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Psychopathological and emotional deficits in myotonic dystrophy

1998

OBJECTIVE—To evaluate psychopathological disturbances in patients with myotonic dystrophy (MD) and compare patients with MD to both patients with facioscapulohumeral dystrophy (FSHD) and healthy control subjects. METHODS—A semistructured interview was used to determine DSM III-R criteria for major depressive episodes, dysthymic episodes, and generalised anxiety. The Montgomery and Asberg and the Hamilton depressive scales, the Covi and Tyrer anxiety scales, the Abrams and Taylor scale for emotional blunting, and the depressive mood scale were all used in the study. Subjects were also asked to complete questionnaires for physical and social anhedonia. RESULTS—Fifteen patients with MD, 11 pat…

AdultMalemedicine.medical_specialtyNeuromuscular diseaseEmotional bluntingbehavioral disciplines and activitiesMyotonic dystrophyDiagnosis DifferentialAdaptation PsychologicalmedicineHumansMyotonic DystrophyAffective SymptomsPsychiatryDepression (differential diagnoses)Defense MechanismsPsychiatric Status Rating ScalesDepressive Disorder MajorDysthymic DisorderSick RoleAnhedoniaMiddle Agedmedicine.diseaseAnxiety DisordersPsychiatry and Mental healthPapersAnxietyFemaleSurgeryNeurology (clinical)Dysthymic Disordermedicine.symptomPsychologyPsychopathologyJournal of Neurology, Neurosurgery & Psychiatry
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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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Isometric muscle contractions after double pulse stimulation. comparison of healthy subjects and patients with myotonic dystrophy.

1996

Isometric contractions of the adductor pollicis muscle were studied in healthy subjects and patients with myotonic dystrophy after single and double stimuli of the ulnar nerve using a wide range of interstimulus intervals (ISI, 0.4-180 ms). In healthy subjects, the force contributed by a second stimulus was greater than the single twitch force being maximal (mean + 140%) at 12-ms ISI. In myotonic dystrophy, the force contributed by the second stimulus was (relative to a reduced twitch amplitude) increased (mean + 204%) with a maximum at 4.8-ms ISI. An abnormal increase of force was only recorded if the single twitch force was clearly reduced. The absolute refractory period of muscle contrac…

AdultMalemedicine.medical_specialtyPhysiologyRefractory periodIsometric exerciseStimulus (physiology)Myotonic dystrophyPhysiology (medical)Internal medicineIsometric ContractionMedicineHumansMyotonic DystrophyOrthopedics and Sports MedicineUlnar nervebusiness.industryPublic Health Environmental and Occupational HealthGeneral MedicineAnatomymedicine.diseaseMyotoniaAdductor pollicis muscleElectric StimulationElectrophysiologyCardiologyFemalemedicine.symptombusinessMuscle contractionEuropean journal of applied physiology and occupational physiology
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Evoked potential study in facio-scapulo-humeral muscular dystrophy.

1997

Nerve conduction velocities (NCVs), somatosensory (SEPs) and auditory evoked potentials (BAEPs) were recorded in 9 patients with facio-scapulo-humeral dystrophy (FSHD) and in 20 age-matched controls. In FSHD patients a significant increase of the nerve distal sensory latencies and of the absolute SEP latencies revealed a subclinical involvement of the afferent sensory pathways, as well as the abnormal slowing of the later components of the BAEPs, pointed to a central auditory dysfunction. Moreover all patients underwent brain MRI that showed the presence of white matter hyperintense lesions in 4 of them (44%). No correlations were found between individual or total number of SEP and BAEP abn…

AdultMalemedicine.medical_specialtyShoulderNeural ConductionSensory systemSomatosensory systemSeverity of Illness IndexNerve conduction velocityMuscular DystrophiesWhite matterInternal medicineEvoked Potentials SomatosensorymedicineEvoked Potentials Auditory Brain StemHumansMuscular dystrophyAuditory Diseases CentralSubclinical infectionChi-Square DistributionDystrophyBrainGenetic VariationGeneral MedicineMiddle Agedmedicine.diseaseMagnetic Resonance ImagingMedian Nervemedicine.anatomical_structureNeurologySomatosensory evoked potentialCase-Control StudiesFaceCardiologyArmFemaleNeurology (clinical)Tibial NervePsychologyNeuroscienceActa neurologica Scandinavica
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Lattice Corneal Dystrophy Type 1

2014

PURPOSE To evaluate the question whether lattice corneal dystrophy type 1 (LCD1) is of epithelial or stromal origin. METHODS The landmark of advanced LCD1 shows central superficial haze and paracentral stromal lattice lines. In 16 eyes of 8 affected individuals of 2 families, a penetrating keratoplasty was performed. The follow-up was 8 to 16 years after penetrating keratoplasty. Slit-lamp documentation of the patients was evaluated in direct and indirect illumination with dilated pupil to assess the horizontal and vertical pattern of new deposits on the corneal graft. Three affected patients of 2 families are demonstrated in detail. A DNA analysis was performed. RESULTS Gene identification…

AdultMalemedicine.medical_specialtyStromal cellCorneal StromaDNA Mutational AnalysisCorneal graftCorneal KeratocytesCorneal erosionDirect illuminationTransforming Growth Factor betaOphthalmologyTGFBI genemedicineHumansCorneal Dystrophies HereditaryExtracellular Matrix Proteinsbusiness.industryEpithelium Cornealmedicine.diseaseeye diseasesOphthalmologyMutationLattice corneal dystrophyFemalebusinessKeratoplasty PenetratingTGFBICornea
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