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Falência ovariana prematura: aspectos genéticos / Premature ovarian failure: genetic aspects
Piazza, Mauri José; Urbanetz, Almir Antonio; Carvalho, Newton Sérgio de.
  • Piazza, Mauri José; Universidade Federal do Paraná. Departamento de Tocoginecologia. Curitiba. BR
  • Urbanetz, Almir Antonio; Universidade Federal do Paraná. Departamento de Tocoginecologia. Curitiba. BR
  • Carvalho, Newton Sérgio de; Universidade Federal do Paraná. Departamento de Tocoginecologia. Curitiba. BR
Femina ; 38(12): 631-636, dez. 2010. tab
Article in Portuguese | LILACS | ID: lil-590574
RESUMO
A falência ovariana prematura exige, para avaliação conveniente dos diversos fenômenos etiológicos envolvidos, adequada análise de seus fatores causais. Entre as possíveis causas genéticas, encontram-se anomalias gênicas ou cromossômicas, seja nos cromossomos X ou nos autossomos. O presente estudo apresenta, de modo sucinto, revisão dos fatores genéticos que são responsáveis por tais fenômenos etiológicos.
ABSTRACT
Premature ovarian failure demands a proper analysis of countless factors for an accurate assessment of the several etiological phenomena processes involved. Among the possible genetic causes, it has been detected genic of chromossomal anomalies, ocurring either on the sex chromosomes or on the autosomes. This study presents a review of the genetic and chromosomal factors which account for etiological phenomena.
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Index: LILACS (Americas) Main subject: Congenital Abnormalities / X Chromosome / Chromosome Aberrations / Primary Ovarian Insufficiency / Genetic Predisposition to Disease / Chromosome Disorders / Genetic Diseases, X-Linked Limits: Female / Humans Language: Portuguese Journal: Femina Journal subject: Gynecology / Obstetrics Year: 2010 Type: Article Affiliation country: Brazil Institution/Affiliation country: Universidade Federal do Paraná/BR

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Index: LILACS (Americas) Main subject: Congenital Abnormalities / X Chromosome / Chromosome Aberrations / Primary Ovarian Insufficiency / Genetic Predisposition to Disease / Chromosome Disorders / Genetic Diseases, X-Linked Limits: Female / Humans Language: Portuguese Journal: Femina Journal subject: Gynecology / Obstetrics Year: 2010 Type: Article Affiliation country: Brazil Institution/Affiliation country: Universidade Federal do Paraná/BR