Search results for "Cystic Change"

showing 3 items of 3 documents

Chondrodysplasia punctata — Rhizomelic form

1976

Pathologic, ultrastructural and radiologic studies are described on 3 infants with the rhizomelic form of chondrodysplasia punctata. Radiologic criteria in the young infant include radiolucent coronal clefts dividing all or most of the thoracic and lumbar vertebral bodies, short humeri with flared metaphyses and punctate calcifications commonly present adjacent to the ossified ischial and pubic bones and less commonly in other locations. In late infancy and childhood the radiologic criteria include demineralization in all bones with slow maturation, flat vertebral bodies, short humeri and femora, metaphyseal flaring, especially in the distal humerus, proximal femur and proximal tibia, immat…

Cartilage ArticularMalemusculoskeletal diseasesChondrodysplasia PunctataPathologymedicine.medical_specialtyContractureDegeneration (medical)Skin DiseasesBone and BonesCataractInfant Newborn DiseasesLumbarmedicineHumansChondrodysplasia punctataFemurChildPelvisCerebral CortexNeuronsbusiness.industryCartilageMetaphyseal flaringInfant NewbornInfantPatellaAnatomyHumerusCystic Changemedicine.diseaseCartilagemedicine.anatomical_structureChild PreschoolPediatrics Perinatology and Child HealthMicrocephalyFemalePsychomotor DisordersbusinessCancellous boneEuropean Journal of Pediatrics
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A pouch in the cervix: a strange diagnosis

2016

Anechoic cervical lesions are uncommon findings which may entail diagnostic and, therefore, management difficulties. Chronic cervicitis, bulky nabothian cysts, adenomyomas, niches (cesarean scar defects), congenital malformations, and pseudo-neoplastic glandular cervical lesions often raise diagnostic dilemmas; they may also mimic malignant lesions [1–4]. Other anechoic images worth considering are those produced by cystic changes after cervical trauma, lacerations, or extremely rare false passages resulting from cervical dilatation [5]. Methods

medicine.medical_specialty030219 obstetrics & reproductive medicinemedicine.diagnostic_testbusiness.industryChronic CervicitisAbnormal uterine bleedingObstetrics and GynecologyInterventional radiologyHysteroscopyCystic Change030218 nuclear medicine & medical imaging03 medical and health sciences0302 clinical medicinemedicine.anatomical_structureCervical cystObstetrics and gynaecologyHysteroscopymedicineSurgeryRadiologyPouchCervical dilatationbusinessCervixGynecological Surgery
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Syndrome of autosomal recessive polycystic kidneys with skeletal and facial anomalies is not linked to the ARPKD gene locus on chromosome 6p

2000

We report on two sibs, both males, one born at 37 the other at 24 weeks of gestation, both with a syndrome similar to that seen in three sets of sibs by Gillessen-Kaesbach et al. [1993: Am J Med Genet 45:511–518]. Both propositi had polycystic kidneys and hepatic fibrosis indistinguishable from that seen in autosomal recessive polycystic kidney disease (ARPKD), and skeletal and facial anomalies. Skeletal abnormalities included “butterfly” vertebrae, square shape of pelvis, and brachymelia. The facial anomalies included hypertelorism, epicanthic folds, and anteverted nares. Additional external findings were apparently low-set ears and a short neck. Histopathological examination of the kidney…

medicine.medical_specialtyPathologyGenetic heterogeneityBiologyCystic Changemedicine.diseaseAutosomal Recessive Polycystic Kidney DiseaseEndocrinologyGenetic linkageInternal medicinemedicineCystHypertelorismmedicine.symptomGenetics (clinical)Potter SyndromeKidney diseaseAmerican Journal of Medical Genetics
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