Search results for "Epiphyses"

showing 8 items of 8 documents

Bone age determination based on the study of the medial extremity of the clavicle

1998

The development of the medial clavicular epiphysis and its fusion with the clavicular shaft have been a subject of medical research since the second decade of this century. Computed tomography provides the imaging modality of choice in analyzing the maturation process of the sternal end of the clavicle. In a retrospective study, we analyzed normal development in 380 individuals under the age of 30 years. The appearance of an epiphyseal ossification center occurred between ages 11 and 22 years. Partial union was found from age 16 until age 26 years. Complete union was first noted at age 22 years and in 100 % of the sample at age 27 years. Based on these data, age-related standardized age dis…

Adultmedicine.medical_specialtyAdolescentComputed tomographyOssification centerReference ValuesAge Determination by SkeletonmedicineHumansRadiology Nuclear Medicine and imagingChildRetrospective StudiesNeuroradiologyOrthodonticsmedicine.diagnostic_testOssificationbusiness.industryInfantRetrospective cohort studyBone ageGeneral MedicineClavicleSurgerymedicine.anatomical_structureClavicleEpiphysisChild PreschoolRadiologymedicine.symptomTomography X-Ray ComputedbusinessEpiphysesEuropean Radiology
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A new type of autosomal recessive spondyloepiphyseal dysplasia tarda

2004

Repeated occurrence of a hitherto unrecognized form of spondyloepiphyseal dysplasia tarda (SED tarda) has been studied in two independent families. Because parental consanguinity was also present in one family, autosomal recessive inheritance is proposed. The onset was in late childhood. The slowly evolving disorder shared several features of the already known types of SED tarda. The radiographic abnormalities were limited to the spine and proximal femora. The patients' hands were normal. The entity described is set apart not only from the X-linked and autosomal-dominant forms of SED tarda but also from the already delineated autosomal recessive types by significant clinical and radiographi…

Malemusculoskeletal diseasesSpondyloepiphyseal dysplasiaSpondyloepiphyseal dysplasia tardamedicine.medical_specialtyAdolescentGenes RecessiveBiologyOsteochondrodysplasiasGenetic linkageMolecular geneticsGenotypemedicineHumansChildGenetics (clinical)Family HealthGeneticsSpondyloepimetaphyseal dysplasiaFemur Headmedicine.diseaseOsteochondrodysplasiaSpineRadiographyParental consanguinityFemaleEpiphysesAmerican Journal of Medical Genetics
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Stippled epiphyses in fetal alcohol syndrome.

1990

We report on punctate epiphyseal calcifications (stippled epiphyses) in the fetal alcohol syndrome and present the differential diagnosis of chondrodysplasia punctata. A literature survey shows that epiphyseal calcifications accompanying alcoholic embryopathy are regularly located in the lower limbs and rarely found in the upper extremities.

musculoskeletal diseasesMaleChondrodysplasia Punctatabusiness.industryFetal alcohol syndromeInfant NewbornCalcinosisStippled epiphysesAnatomymedicine.diseaseDiagnosis DifferentialRadiographyFetal Alcohol Spectrum DisordersPediatrics Perinatology and Child HealthmedicineHumansRadiology Nuclear Medicine and imagingChondrodysplasia punctataDifferential diagnosisLiterature surveybusinessPediatric radiology
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Three-dimensional distribution of trabecular bone density and cortical thickness in the distal humerus

2008

One major barrier to osteosynthesis in distal humeral fractures is poor bone quality. This study was an attempt to measure the bone quality in the distal humerus.We measured the distribution of total bone mineral density (BMD), trabecular BMD (tBMD), and cortical thickness (CTh) in the distal humerus using peripheral quantitive computed tomography. Four slices in the infracondylar, supracondylar, and distal disphyseal regions of 25 human cadaver humeri were investigated.Total BMD decreased continuously from the distal diaphysis to the trochlea. Within the infracondylar region, the capitellum was the region of lowest tBMD and CTh (P.001). Measurements in anterior regions were higher than in …

AdultMaleHumeral FracturesSensitivity and SpecificityAbsorptiometry PhotonImaging Three-DimensionalSex FactorsBone DensityCadaverElbow JointImage Interpretation Computer-AssistedCadaverConfidence IntervalsmedicineHumansOrthopedics and Sports MedicineHumerusQuantitative computed tomographyAgedProbabilityAged 80 and overBone mineralOsteosynthesismedicine.diagnostic_testbusiness.industryAge FactorsReproducibility of ResultsImplant failureGeneral MedicineAnatomyHumerusMiddle AgedDiaphysismedicine.anatomical_structureBone TrabeculaeFemaleSurgeryDiaphysesTomography X-Ray ComputedElbow InjuriesbusinessEpiphysesJournal of Shoulder and Elbow Surgery
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Short review: Field recovery and potential information value of small elements of the skeleton

2011

The recovery of small elements of the skeleton (e.g. hyoid, carpals, and hand and foot phalanges) is one of the established tasks of the archaeologist and physical anthropologist when working in the field, whether in an archaeological or forensic context. In the present work, we illustrate the field location of ossified laryngeal cartilages, hand sesamoids, and the medial clavicular epiphyses. The potential information offered by these elements is briefly summarized. The frequency of these elements observed in a cemetery dating from 1943 indicates the possibility that these elements could be found in other contexts at a higher frequency than expected.

AdultMaleHistoryLaryngeal CartilagesContext (language use)Laryngeal cartilageSkeleton (category theory)Bone and BonesAnthropology PhysicalYoung AdultOsteogenesisHumansCemeteriesInformation valuePrisonersHistory 20th CenturyPhalanxClavicleArchaeologyField (geography)ArchaeologySpainAnthropologySesamoid BonesEpiphysesCognitive psychologyHOMO
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Complex radial head and neck fractures treated with modern locking plate fixation

2019

Background Internal fixation of complex radial head and neck (CRHN) fractures is difficult, and postoperative complications are common. This study evaluated elbow function and patient clinical status after internal fixation of CRHN fractures with modern locking plates. Methods We included 40 patients with 41 fractures (1 bilateral lesion). In 25 patients (61%), a concomitant injury was found. Patients were an average age of 46 years (range, 22-70 years). The mean follow-up time was 36 months (range, 2-70 months). Postoperative assessments included evaluation of range of motion, functional scores, and radiologic findings. We assessed fracture healing, surgical complications, revision surgery…

AdultMaleReoperationmedicine.medical_specialtyJoint replacementmedicine.medical_treatmentElbowBone healingSupinationFracture Fixation InternalYoung Adult03 medical and health sciencesFixation (surgical)0302 clinical medicineElbow JointHumansMedicineInternal fixationPronationOrthopedics and Sports MedicineRange of Motion ArticularDevice RemovalAgedFracture Healing030222 orthopedicsbusiness.industry030229 sport sciencesGeneral MedicineMiddle AgedSurgeryTreatment Outcomemedicine.anatomical_structureConcomitantFemaleSurgeryRadial head fractureRadius FracturesbusinessRange of motionBone PlatesEpiphysesFollow-Up StudiesJournal of Shoulder and Elbow Surgery
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Identification of Novel pro-α2(IX) Collagen Gene Mutations in Two Families with Distinctive Oligo-Epiphyseal Forms of Multiple Epiphyseal Dysplasia

1999

Multiple epiphyseal dysplasia (MED) is a genetically heterogeneous disorder with marked clinical and radiographic variability. Traditionally, the mild "Ribbing" and severe "Fairbank" types have been used to define a broad phenotypic spectrum. Mutations in the gene encoding cartilage oligomeric-matrix protein have been shown to result in several types of MED, whereas mutations in the gene encoding the alpha2 chain of type IX collagen (COL9A2) have so far been found only in two families with the Fairbank type of MED. Type IX collagen is a heterotrimer of pro-alpha chains derived from three distinct genes-COL9A1, COL9A2, and COL9A3. In this article, we describe two families with distinctive ol…

MaleAdolescentRNA SplicingMutantGene mutationBiologyOsteochondrodysplasiasmedicine.disease_causeMultiple epiphyseal dysplasia03 medical and health sciencesExon0302 clinical medicineOsteoarthritismedicineGeneticsHumansGenetics(clinical)Genetic TestingOsteochondrodysplasiaMultiple epiphyseal dysplasiaGene mutationAlleleChildPolymorphism Single-Stranded ConformationalGenetics (clinical)030304 developmental biologyGenetics0303 health sciencesMutationType IX collagenGenetic heterogeneitymedicine.diseaseOsteochondrodysplasiaPedigreeRadiographyCartilageChild PreschoolMutationFemaleEpiphysesProcollagen030217 neurology & neurosurgeryResearch ArticleThe American Journal of Human Genetics
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Symptomatische Verkalkungen beim Neugeborenen

1990

Stippled epiphyses occur in the new-born and young infant in the different hereditary forms of chondrodysplasia punctata. Symptomatic stippling has been described also in association with chromosomal anomalies, gangliosidosis and drug induced embryopathies. We present patients with Cumarin-embryopathy (2), fetal alcohol syndrome (1), Zellweger-syndrome (2) and chromosomal anomaly 16 (1) and discuss the typical roentgenographic features, distribution and differential diagnosis of epiphyseal stippling.

Stippling (dentistry)Pathologymedicine.medical_specialtybusiness.industryStippled epiphysesAnatomyGangliosidosismedicine.diseaseOsteochondrodysplasiamedicineRadiology Nuclear Medicine and imagingChondrodysplasia punctataDifferential diagnosisbusinessEpiphyseal stipplingCalcificationRöFo - Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebenden Verfahren
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