2017
DOI: 10.5935/1676-2444.20170017
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Report of a patient with fragile X syndrome unexpectedly identified by karyotype analysis

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Cited by 3 publications
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“…There are proven alterations at family levels, such as learning difficulties, intellectual disability, movement disorders and primary ovarian insufficiency, which may be warnings of a protein mutation related to FXS resulting from its family origin [14] . Currently, the test of choice for diagnosing FXS per American College guidelines of Medical Genetics are molecular DNA tests, Southern blot test , polymerase chain reaction (PCR), or even by the cytogenetic technique [15] .…”
Section: Literature Reviewmentioning
confidence: 99%
“…There are proven alterations at family levels, such as learning difficulties, intellectual disability, movement disorders and primary ovarian insufficiency, which may be warnings of a protein mutation related to FXS resulting from its family origin [14] . Currently, the test of choice for diagnosing FXS per American College guidelines of Medical Genetics are molecular DNA tests, Southern blot test , polymerase chain reaction (PCR), or even by the cytogenetic technique [15] .…”
Section: Literature Reviewmentioning
confidence: 99%
“…Quanto ao diagnóstico em homens, este era realizado indiretamente pelo método de reação de cadeia polimerase (PCR), porém este método não é suficiente para indicar a mutação do gene em mulheres. Em vista disso, em pessoas do sexo feminino, são utilizados os métodos southern blot e de hibridização para o diagnóstico final da síndrome 7,9 .…”
Section: Revisão De Literaturaunclassified