The psychiatric presentation of fragile x: evolution of the diagnosis and treatment of the psychiatric comorbidities of fragile X syndrome
MR Tranfaglia�- Developmental neuroscience, 2011 - karger.com
Fragile X syndrome (FXS) is the leading inherited cause of mental retardation and autism
spectrum disorders worldwide. It presents with a distinct behavioral phenotype which�…
spectrum disorders worldwide. It presents with a distinct behavioral phenotype which�…
Fragile X syndrome: a psychiatric perspective
MR Tranfaglia�- Modeling fragile X syndrome, 2012 - Springer
Fragile X syndrome (FXS) is associated with a complex but relatively consistent psychiatric
phenotype. Recent research has suggested neural substrates for the behavioral�…
phenotype. Recent research has suggested neural substrates for the behavioral�…
Neuropsychiatric symptoms of fragile X syndrome: pathophysiology and pharmacotherapy
JA Tsiouris, WT Brown�- CNS drugs, 2004 - Springer
Fragile X syndrome is the leading inherited form of mental retardation, and second only to
Down's syndrome as a cause of mental retardation attributable to an identifiable genetic�…
Down's syndrome as a cause of mental retardation attributable to an identifiable genetic�…
Fragile X syndrome: lifespan developmental implications for those without as well as with intellectual disability
J Turk�- Current opinion in psychiatry, 2011 - journals.lww.com
Findings from genetic, neurological, biochemical, psychological and pharmacological
research are combining to revolutionize understanding of the pathogenesis of�…
research are combining to revolutionize understanding of the pathogenesis of�…
Fragile X syndrome: psychiatric manifestations, assessment and emerging therapies
PM Wadell, RJ Hagerman…�- Current Psychiatry�…, 2013 - ingentaconnect.com
Fragile X Syndrome (FXS), the most common inherited cause of intellectual disabilities, is an
X-linked dominant disorder caused by the amplification of a CGG repeat in the�…
X-linked dominant disorder caused by the amplification of a CGG repeat in the�…
Psychiatric and autistic comorbidity in fragile X syndrome across ages
LV Gabis, YK Baruch, A Jokel…�- Journal of child�…, 2011 - journals.sagepub.com
Fragile X syndrome is caused by CGG trinucleotide repeat expansion within the fragile X
mental retardation 1 gene, when repeat number exceeds 200. The typical psychiatric profile�…
mental retardation 1 gene, when repeat number exceeds 200. The typical psychiatric profile�…
Fragile X syndrome
RJ Hagerman, E Berry-Kravis, HC Hazlett…�- Nature reviews Disease�…, 2017 - nature.com
Fragile X syndrome (FXS) is the leading inherited form of intellectual disability and autism
spectrum disorder, and patients can present with severe behavioural alterations, including�…
spectrum disorder, and patients can present with severe behavioural alterations, including�…
Neuroanatomical, molecular genetic, and behavioral correlates of fragile X syndrome
SD Koukoui, A Chaudhuri�- Brain research reviews, 2007 - Elsevier
Fragile X syndrome (FXS) is a leading cause of inherited mental retardation. In the vast
majority of cases, this X-linked disorder is due to a CGG expansion in the 5′ untranslated�…
majority of cases, this X-linked disorder is due to a CGG expansion in the 5′ untranslated�…
Translational endpoints in fragile X syndrome
CEF de Esch, S Zeidler, R Willemsen�- Neuroscience & Biobehavioral�…, 2014 - Elsevier
Fragile X syndrome (FXS) occurs in less than 10% of the intellectually disabled (ID)
population. The cause of FXS is a CGG trinucleotide repeat longer than 200 CGG units�…
population. The cause of FXS is a CGG trinucleotide repeat longer than 200 CGG units�…
Fragile X syndrome: A review of clinical management
R Lozano, A Azarang, T Wilaisakditipakorn…�- Intractable & rare�…, 2016 - jstage.jst.go.jp
The fragile X mental retardation 1 gene, which codes for the fragile X mental retardation 1
protein, usually has 5 to 40 CGG repeats in the 5'untranslated promoter. The full mutation is�…
protein, usually has 5 to 40 CGG repeats in the 5'untranslated promoter. The full mutation is�…