Presymptomatic genetic testing in minors at risk of paraganglioma and pheochromocytoma: Our experience of oncogenetic multidisciplinary consultation

Hormone and Metabolic Research

Volumn 44, Issue 5, 2012, Pages 354-358

  Lahlou Laforet K ^a,b   Consoli, S M ^a,b   Jeunemaitre, X ^a,b,c   Gimenez Roqueplo, A P ^a,b,c  

^a HÔPITAL EUROPÉEN GEORGES POMPIDOU   (France)

^b UNIVERSITÉ PARIS DESCARTES   (France)

^c PARIS CARDIOVASCULAR RESEARCH CENTER   (France)

Author keywords

genetic counseling; minors; parents; predictive genetic testing

Indexed keywords

ARTICLE; CANCER RISK; CANCER SCREENING; CHILD; CLINICAL ARTICLE; EMOTION; FAMILIAL CANCER; FEMALE; GENE MUTATION; GENETIC PREDISPOSITION; GENETIC RISK; GENETIC SCREENING; HEALTH BEHAVIOR; HETEROZYGOTE; HUMAN; JUVENILE; MALE; PARAGANGLIOMA; PARENT; PHEOCHROMOCYTOMA; PRESYMPTOMATIC GENETIC SCREENING; PRIORITY JOURNAL; SCHOOL CHILD;

ADOLESCENT; ADRENAL GLAND NEOPLASMS; CHILD; CHILD, PRESCHOOL; FEMALE; GENETIC COUNSELING; GENETIC TESTING; HUMANS; MALE; MINORS; PARAGANGLIOMA; PARENTS; PHEOCHROMOCYTOMA; PROSPECTIVE STUDIES; RISK FACTORS;

EID: 84860839470     PISSN: 00185043     EISSN: 14394286     Source Type: Journal    
DOI: 10.1055/s-0032-1311568     Document Type: Article

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