Genotype-phenotype associations in PPGLs in 59 patients with variants in SDHX genes

Keyphrases

• Tumor 100%
• Genotype-phenotype Association 100%
• Pheochromocytoma 100%
• Paraganglioma 100%
• Clinical Characteristics 66%
• Early Detection 66%
• Genetic Variants 66%
• Genetic Factors 33%
• Pathogenic Variants 33%
• Tertiary Care Hospital 33%
• Family Members 33%
• Histopathological Features 33%
• Clinical Follow-up 33%
• Proband 33%
• Clinical Genetics 33%
• Pathological Findings 33%
• Early Diagnosis 33%
• Clinical Risk Stratification 33%
• Genetic Screening 33%
• Underlining 33%
• Clinical Phenotype 33%
• Rare Variants 33%
• Sympathetic Nervous System 33%
• Catecholamines 33%
• Clinical Factors 33%
• Better Prognosis 33%
• Family Screening 33%
• Malignant Pheochromocytoma 33%
• Extra-adrenal 33%
• Malignant Phenotype 33%
• Systematic Screening 33%
• Adrenal Medulla 33%
• Phenotypical 33%
• Germline Variants 33%
• Biochemical Factors 33%
• Tumor Screening 33%
• Variant Phenotypes 33%
• Familial Paraganglioma 33%
• Poor Prognostic Marker 33%
• Combined Algorithm 33%
• Morphological Factors 33%

Biochemistry, Genetics and Molecular Biology

• Genotyping 100%
• SDHB 100%
• Genetic Divergence 66%
• SDHA 66%
• Catecholamine 33%
• Genetics 33%
• Cohort Study 33%
• Morphology 33%
• Genetic Screening 33%
• Germline 33%
• Germ Cell 33%
• Proband 33%
• SDHD 33%