mutations in methyl - CpG - binding protein 2 ( MECP2(passive) caused bya severe childhood onset neurodevelopmental disorder
mutations in the autoimmune regulator ( AIRE ) gene , including the distinctive R139X in Sardinia(passive) caused bya childhood - onset monogenic disorder
The American Psychiatric Associationcreatedchildhood - onset fluency disorder
a point mutation in position 1824 of the LMNA gene , replacing cytosine with thymine , creating an unusable form of the protein(passive) caused bychildhood disorder
50 X - linked recessive mutationscauseserious childhood - onset disorders
28 X - linked recessive mutationscauseserious childhood - onset disorders
to aggressive or disruptive behaviors , which interfere with learning and peer relationships ... in turn leading to low self - esteem and further behavioral problems ... Additional , kids whose mothers had an existing mental health trouble or stern parenting stress were two - and - a - half times much probable to display emotional - behavioral issuescan leadto aggressive or disruptive behaviors , which interfere with learning and peer relationships ... in turn leading to low self - esteem and further behavioral problems ... Additional , kids whose mothers had an existing mental health trouble or stern parenting stress were two - and - a - half times much probable to display emotional - behavioral issues
multiple domains of adaptive functioning throughout the lifespaninfluencingmultiple domains of adaptive functioning throughout the lifespan
to aggressive or disruptive behaviours , which interfere with learning and peer relationships ... in turn leading to low self - esteem and further behavioural problemscan leadto aggressive or disruptive behaviours , which interfere with learning and peer relationships ... in turn leading to low self - esteem and further behavioural problems
progressive sensory and muscle losscausesprogressive sensory and muscle loss
him to stutter and have anxietycausedhim to stutter and have anxiety
innephrotic syndrome , which includes massive proteinuria , hypoalbuminemia , hyperlipidemia , and edemaresultinginnephrotic syndrome , which includes massive proteinuria , hypoalbuminemia , hyperlipidemia , and edema
oftenleadsoften
in nephrotic syndrome , which includes massive proteinuria , hypoalbuminemia , hyperlipidemia , and edemaresultingin nephrotic syndrome , which includes massive proteinuria , hypoalbuminemia , hyperlipidemia , and edema