Malan syndrome (MALNS) is an ultra-rare genetic disorder caused by heterozygous chromosomal microdeletions involving the 19p13.2 region or loss-of-function variants in the NFIX gene. It is characterized by specific phenotypical features, intellectual disability (ID), and limitations in adaptive functioning and behavioral problems. In a previous work, we defined the cognitive, adaptive, linguistic and visuomotor ability profiles in a group of 15 MALNS individuals, providing quantitative data from standardized evaluations. Here, we further extend the characterization of MALNS by analyzing the behavioral and psychopathological comorbidities of the same cohort, administering standardized tests. Children were evaluated from October 2020 to Janua...
Background Ultrarare Marshall-Smith and Malan syndromes, caused by changes of the gene nuclear facto...
The 22q13.3 deletion syndrome is a neurodevelopmental disorder that includes general hypotonia, deve...
Behavioural correlates of specific genetic conditions are increasingly researched. Such research is ...
Malan Syndrome (MS) is an ultra-rare overgrowth genetic syndrome due to heterozygous variants or del...
Thesis abstract:The current thesis aimed to explore the psychological and behavioural profile of spe...
Background: Ultrarare Marshall–Smith and Malan syndromes, caused by changes of the gene nuclear fact...
International audienceMalan syndrome is an overgrowth disorder described in a limited number of indi...
Background: Ultrarare Marshall-Smith and Malan syndromes, caused by changes of the gene nuclear fact...
Motor disturbances have been widely observed in children with autism spectrum disorder (ASD), and mo...
BackgroundPhelan-McDermid syndrome (PMS) or 22q13.3 deletion syndrome is a rare genetic disorder cha...
Background Ultrarare Marshall-Smith and Malan syndromes, caused by changes of the gene nuclear facto...
The 22q13.3 deletion syndrome is a neurodevelopmental disorder that includes general hypotonia, deve...
Behavioural correlates of specific genetic conditions are increasingly researched. Such research is ...
Malan Syndrome (MS) is an ultra-rare overgrowth genetic syndrome due to heterozygous variants or del...
Thesis abstract:The current thesis aimed to explore the psychological and behavioural profile of spe...
Background: Ultrarare Marshall–Smith and Malan syndromes, caused by changes of the gene nuclear fact...
International audienceMalan syndrome is an overgrowth disorder described in a limited number of indi...
Background: Ultrarare Marshall-Smith and Malan syndromes, caused by changes of the gene nuclear fact...
Motor disturbances have been widely observed in children with autism spectrum disorder (ASD), and mo...
BackgroundPhelan-McDermid syndrome (PMS) or 22q13.3 deletion syndrome is a rare genetic disorder cha...
Background Ultrarare Marshall-Smith and Malan syndromes, caused by changes of the gene nuclear facto...
The 22q13.3 deletion syndrome is a neurodevelopmental disorder that includes general hypotonia, deve...
Behavioural correlates of specific genetic conditions are increasingly researched. Such research is ...