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Abnormalities, MultipleChromosome AberrationsCongenital AbnormalitiesChromosome DisordersEye AbnormalitiesKaryotypingMagnetic Resonance ImagingBrainCardiovascular AbnormalitiesCraniofacial AbnormalitiesSyndromeSkin AbnormalitiesPhenotypeUrogenital AbnormalitiesPregnancyTrisomyMutationMusculoskeletal AbnormalitiesIn Situ Hybridization, FluorescenceTooth AbnormalitiesTranslocation, GeneticInfant, NewbornAneuploidyElectrocardiographyDisease Models, AnimalSex Chromosome AberrationsRetrospective StudiesAbnormalities, Drug-InducedCase-Control StudiesTime FactorsFetal DiseasesSchizophreniaPedigreeProspective StudiesCytogenetic AnalysisBrain DiseasesTomography, X-Ray ComputedMice, KnockoutUltrasonography, PrenatalChromosome DeletionHeart Defects, CongenitalSensitivity and SpecificityImage Processing, Computer-AssistedChromosome BandingFollow-Up StudiesCytogeneticsPrenatal DiagnosisNervous System MalformationsEchocardiographyMice, TransgenicMice, Mutant StrainsPrognosisHomozygoteRisk FactorsMice, Inbred C57BLHeterozygoteIntellectual DisabilityChromosomes, Human, Pair 13Reference ValuesBiopsyPredictive Value of TestsAgenesis of Corpus CallosumDown SyndromeDigestive System AbnormalitiesElectroencephalographyAtrophyLimb Deformities, CongenitalMosaicismChromosomes, Human, Pair 11Neurologic ExaminationDiffusion Magnetic Resonance ImagingOcular Motility DisordersMyelodysplastic SyndromesGestational AgeAbnormal KaryotypeNerve Fibers, MyelinatedGene DeletionHeartInfertility, MaleAnalysis of VarianceBlood Coagulation DisordersChromosomes, Human, Pair 7Cerebral CortexImmunohistochemistrySeverity of Illness IndexHeart DiseasesMolecular Sequence DataBase SequencePrevalenceNervous System DiseasesCorpus CallosumCohort StudiesAcute DiseaseAge FactorsTreatment OutcomeTomography, Emission-Computed, Single-PhotonReproducibility of ResultsAnisotropyDisease ProgressionDNA Mutational Analysis
Atypical teratCongenital AbnormalitiesUROGENITAL SYSTEMDrug-InducedStructural abnormalitiesRhabdoidRhabdoid tumorsAtypicalMutationsRareRisk
Atypical terat2
  • An atypical teratoid rhabdoid tumor (AT/RT) is a rare tumor usually diagnosed in childhood. (wikipedia.org)
  • PRIMARY OBJECTIVES - To estimate the sustained objective response rate and disease stabilization in pediatric patients with recurrent or progressive AT/RT (atypical teratoid rhabdoid tumor in the CNS) (Stratum A1) treated with alisertib and to determine if the response is sufficient to merit continued investigation of alisertib in this population. (stanford.edu)
Congenital Abnormalities1
  • Congenital abnormalities caused by medicinal substances or drugs of abuse given to or taken by the mother, or to which she is inadvertently exposed during the manufacture of such substances. (wakehealth.edu)
UROGENITAL SYSTEM1
  • Congenital structural abnormalities of the UROGENITAL SYSTEM in either the male or the female. (ctsicn.org)
Drug-Induced3
  • Abnormalities, Drug-Induced" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings) . (wakehealth.edu)
  • This graph shows the total number of publications written about "Abnormalities, Drug-Induced" by people in this website by year, and whether "Abnormalities, Drug-Induced" was a major or minor topic of these publications. (wakehealth.edu)
  • Below are the most recent publications written about "Abnormalities, Drug-Induced" by people in Profiles. (wakehealth.edu)
Structural abnormalities1
  • Congenital or acquired structural abnormalities of the lymphatic system ( LYMPHOID TISSUE ) including the lymph vessels. (nih.gov)
Rhabdoid2
  • Atypical teratoid/rhabdoid tumors are very rare, and absolute risk to siblings is not reported in the literature. (wikipedia.org)
  • Immunohistological detection of BCOR was performed in eight pineoblastoma, five germinoma and four atypical teratoid rhabdoid tumours (ATRTs), all located in the pineal region. (bvsalud.org)
Rhabdoid tumors3
  • In families with this mutation, researchers have identified the development of both renal and extrarenal malignant rhabdoid tumors, choroid plexus carcinomas, atypical teratoid rhabdoid tumors, and medulloblastomas. (medscape.com)
  • [ 6 , 7 ] It therefore has been suggested that tumors believed to be choroid plexus carcinomas with hSNF5/INI1 mutations may actually be atypical teratoid rhabdoid tumors. (medscape.com)
  • Atypical teratoid/rhabdoid tumors are very rare, and absolute risk to siblings is not reported in the literature. (wikipedia.org)
Atypical1
  • An atypical teratoid rhabdoid tumor (AT/RT) is a rare tumor usually diagnosed in childhood. (wikipedia.org)
Mutations1
  • Among 525 individuals with Covid-19 from Memorial Sloan Kettering (MSK) and the Korean Clonal Hematopoiesis (KoCH) consortia, we show that CH is associated with severe Covid-19 outcomes (OR = 1.85, 95%=1.15-2.99, p = 0.01), in particular CH characterized by non-cancer driver mutations (OR = 2.01, 95% CI = 1.15-3.50, p = 0.01). (nature.com)
Rare1
  • The constitutional 9p duplication is another rare abnormality whose association with choroid plexus hyperplasia and choroid plexus papilloma has been reported. (medscape.com)
Risk2
  • These findings suggest a relationship between CH and risk of severe infections that warrants further investigation. (nature.com)
  • Here, we show that CH is associated with an increased risk of severe Covid-19 outcomes in a cohort of solid tumor patients and healthy individuals. (nature.com)