The 6th Annual International PTEN Symposium: From Patient-Centered Research to Clinical Care
第六届国际 PTEN 研讨会:从以患者为中心的研究到临床护理
基本信息
- 批准号:10683454
- 负责人:
- 金额:$ 1.68万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2023
- 资助国家:美国
- 起止时间:2023-03-20 至 2024-02-29
- 项目状态:已结题
- 来源:
- 关键词:AddressAdultAffectAgeAwarenessBenignBiologyBlood VesselsCaregiversCaringChildhoodClinicClinicalClinical ResearchClinical TrialsCommunitiesComplexComprehensive Health CareCountryDermatologyDevelopmentDiagnosisDiseaseEducationEndocrinologyEtiologyEvaluationEventFacultyFamilyFoundationsGastroenterologyGeneticGenetic CounselingGenetic DiseasesGenomic medicineGenomicsGerm-Line MutationGrowthGuidelinesHealth PersonnelHealth ProfessionalHealthcareHearingHereditary Breast CarcinomaHybridsIndividualInstitute of Medicine (U.S.)Internal MedicineInternationalKnowledgeLearningLongevityMalignant Female Reproductive System NeoplasmMalignant NeoplasmsMedical GeneticsModelingMutationNephrologyNeurodevelopmental DisorderNeurologicNeurologyNurse PractitionersNursesOhioOncologyOrganPTEN Hamartoma Tumor SyndromePTEN genePatient CarePatient-Focused OutcomesPatientsPediatricsPersonsPhysician AssistantsPhysiciansProviderPsychiatryPsychologyResearchResearch PersonnelRiskScienceSpecialistStressStudentsTherapeuticTranslational ResearchTumor Suppressor GenesUpdateUrologyWomen&aposs Healthautism spectrum disordercancer riskcase-basedclinical carecopingexperiencefollow-upgenetic counselorimprovedinterestlive streammedical specialtiesmembermultidisciplinarypatient orientedprecision geneticsprogramsrare genetic disorderresiliencescreeningsymposiumvirtual
项目摘要
Project Summary: The 6th Annual International PTEN Symposium: From Patient-Centered
Research to Clinical Care will review the latest scientific and clinical advances in PTEN
hamartoma tumor syndrome (PHTS), a rare genetic condition caused by germline mutations in
the PTEN gene that is associated with an increased risk for certain cancers and benign growths
and is one of the most common etiologies for neurodevelopmental conditions, including autism
spectrum disorder. Presented by Cleveland Clinic’s Genomic Medicine Institute and Center for
Personalized Genetic Healthcare and endorsed by the PTEN Hamartoma Tumor Syndrome
Foundation and PTEN Italia, the symposium will offer state-of-the-art information to healthcare
providers treating patients with germline PTEN mutations and provide a forum for members of
the PHTS patient community to connect and learn about cutting-edge PTEN research as well as
clinical surveillance and management guidelines. PHTS is a rare, complex disorder affecting
multiple organs over the lifespan with differing manifestations based on age. Patients with a
PTEN mutation require lifetime follow-up for neurological concerns and cancer risk surveillance
as well as familial screening and evaluation. A comprehensive care model that includes both
pediatric and adult specialists familiar with this condition and prepared to provide optimal care is
necessary. Unfortunately, PHTS is not well known to many clinicians throughout the world. To
address this knowledge gap, the program is centered on the following learning objectives: (1)
describe current PTEN translational and clinical research, (2) apply research information about
PHTS to diagnosis, screening, surveillance, guidelines, patient needs, clinical features and
coordination of multidisciplinary team care and (3) demonstrate awareness and share education
about PHTS, leading to timely diagnosis, appropriate surveillance and improved patient
outcomes. Expert Cleveland Clinic and guest faculty will share research and case-based
presentations highlighting the advances of genetics and genomics of PHTS and the science of
PTEN. Topics include PTEN biology and therapeutics, neurodevelopmental disorders,
hereditary breast cancer, gynecological cancer, updates on PTEN research and clinical trials,
PTEN-related vascular anomalies, and stress and resilience in coping with PHTS. The program
also will incorporate a patient experience panel, which will provide the opportunity to hear
unique patient perspectives on PHTS. The symposium will be held as a live one-day event on
March 27, 2023, at the InterContinental Hotel and Bank of America Conference Center in
Cleveland, Ohio and will be available to virtual attendees via a livestream.
项目总结:第六届国际PTEN年会:从患者为中心
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Charis Eng其他文献
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{{ truncateString('Charis Eng', 18)}}的其他基金
Modeling Autism and Comorbid Cancer Risk in Individuals with Germline PTEN Mutations
种系 PTEN 突变个体的自闭症和共病癌症风险建模
- 批准号:
10704496 - 财政年份:2022
- 资助金额:
$ 1.68万 - 项目类别:
Modeling Autism and Comorbid Cancer Risk in Individuals with Germline PTEN Mutations
种系 PTEN 突变个体的自闭症和共病癌症风险建模
- 批准号:
10358435 - 财政年份:2022
- 资助金额:
$ 1.68万 - 项目类别:
Natural history of individuals with autism spectrum disorder and germline PTEN mutations
患有自闭症谱系障碍和种系 PTEN 突变的个体的自然史
- 批准号:
10242080 - 财政年份:2014
- 资助金额:
$ 1.68万 - 项目类别:
Natural history of individuals with autism spectrum disorder and germline PTEN mutations
患有自闭症谱系障碍和种系 PTEN 突变的个体的自然史
- 批准号:
10701741 - 财政年份:2014
- 资助金额:
$ 1.68万 - 项目类别:
Deep Sequencing Instrumentation Upgrade - Illumina HiSeq2500
深度测序仪器升级 - Illumina HiSeq2500
- 批准号:
8640603 - 财政年份:2014
- 资助金额:
$ 1.68万 - 项目类别:
Metagenomic profiling of oral polymicrobial flora in head and neck cancers
头颈癌口腔多微生物菌群的宏基因组分析
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8142045 - 财政年份:2010
- 资助金额:
$ 1.68万 - 项目类别:
Genetic Alterations that Initiate Follicular Thyroid Carcinogenesis
引发滤泡性甲状腺癌的基因改变
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8505981 - 财政年份:2008
- 资助金额:
$ 1.68万 - 项目类别:
Genetic Alterations that Initiate Follicular Thyroid Carcinogenesis
引发滤泡性甲状腺癌的基因改变
- 批准号:
8697754 - 财政年份:2008
- 资助金额:
$ 1.68万 - 项目类别:
Genetic Alterations that Initiate Follicular Thyroid Carcinogenesis
引发滤泡性甲状腺癌的基因改变
- 批准号:
9041528 - 财政年份:2008
- 资助金额:
$ 1.68万 - 项目类别:
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