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by respiratory syncytial virus ( RSV(passive) mainly caused byAcute bronchiolitis in infancy
severe pathologiesleadingto death in infancy
the most common birth defectleadingto death in infancy
a male infant to be born with muscle weakness which includes difficulty breathingleadingto death in infancy
CCP1causesinfantile - onset neurodegeneration
Loss of tubulin deglutamylase CCP1causesinfantile - onset neurodegeneration
High concentration of nitrate in drinking water has been foundto causemethaemoglobinaemia in infants
vaccines for diseasescould causeharm in infancy
Title Loss of tubulin deglutamylase CCP1causesinfantile - onset neurodegeneration
how genes , brain development , behaviour , and environment interactto influencedevelopment from infancy
the factorsinfluencegrowth in infancy
practicesinfluencegrowth in infancy
drugmay causeimmunosuppression in the infant
HirshbergledStonyfield from Stonyfield's infancy
Mitochondrial diseasecan causeinfantile - onset HCM
loss - of - function mutationscausehyperinsulinaemic hypoglycaemia of infancy
An iodine deficiency late in pregnancy orleadsearly infancy
a dramasettowards the infancy
Iodine deficiency during pregnancy andcan resultearly infancy
An iodine deficiency during pregnancy andcan resultearly infancy
by infection with S. marcescens(passive) caused byearly infancy
a series of inborn reflexes(passive) is influenced byEarly infancy
any drugcausingCONVULSION IN CHILDHOOD
disorderscausingstridor in infancy
pediatric disorderscausingstridor in infancy
chronic malnutrition , parasitic infections , or genetic defects(passive) is usually caused byCobalamin , Cbl ) in childhood
by a point mutation ( L205P ) in the tyrosine hydroxylase gene(passive) caused byve parkinsonism in infancy
CBS deficiencycausesnearsightedness in infancy
have been shownto causehyperinsulinemia of Infancy
stimulate excessive insulin secretionleadingto hyperinsulinism of infancy
that decreasedmay causePT in infancy
Loss of ERK2 in the telencephaloncausesprecocious neurogenesis
not latermay originateaccumulating in infancy
the factorsinfluencein infancy
whose problemsoriginatein infancy
a developmental disorderoriginatingin infancy
mutationscausein infancy
premature birth , very low birth weight , the use of nicotine , alcohol , or drugs during pregnancy , and severe deficits in nutrition or exposureto leadin infancy
More information ... a rare genetic diseaseis ... discoveredin infancy
the diseaseis discoveredin infancy
to stunted developmentcan leadto stunted development
to learning disabilitiescan leadto learning disabilities
hydrocephaluscan causehydrocephalus
alsocould ... contributealso
to obesity in adulthoodleadsto obesity in adulthood
to obesityleadsto obesity
to a higher risk of obesity later in lifecan leadto a higher risk of obesity later in life
in the slow motor development and progressive enlargement of the skullresultingin the slow motor development and progressive enlargement of the skull
to physical and mental stuntingleadsto physical and mental stunting
to a worse outcomemay leadto a worse outcome
to higher risk of disease , disability and death in childhood and across their lifespanleadingto higher risk of disease , disability and death in childhood and across their lifespan
as a text for college courses at the two- and four - year levelsdesignedas a text for college courses at the two- and four - year levels
to chronic disease and lifelong disabilitiescan leadto chronic disease and lifelong disabilities
to childhood obesity and diabetescontributingto childhood obesity and diabetes
in childhoodcausein childhood
it in childhoodcauseit in childhood
to a worse outcome and may need more complex surgery to fix the problemmay leadto a worse outcome and may need more complex surgery to fix the problem
to inflammation in the arealeadingto inflammation in the area
from bilateral corneal opacificationresultingfrom bilateral corneal opacification
some developmental delays(passive) caused bysome developmental delays
poor growth and a particular type of kidney damage ( renal Fanconi syndrome ) in which certain molecules that should be reabsorbed into the bloodstream are instead eliminated in the urinecausingpoor growth and a particular type of kidney damage ( renal Fanconi syndrome ) in which certain molecules that should be reabsorbed into the bloodstream are instead eliminated in the urine
to mental retardationledto mental retardation
to mental retardationledto mental retardation
to a delay in motor milestonescontributingto a delay in motor milestones
persistent changes that last into adulthoodis causingpersistent changes that last into adulthood
to attitudesleadingto attitudes
paindoes ... causepain
to adverse cognitive and psychological effects , including delayed attention and social withdrawalcan leadto adverse cognitive and psychological effects , including delayed attention and social withdrawal
in such painmay resultin such pain
in failure to achieve motor milestones and in death or the need for mechanical ventilation by 2 years of ageresultsin failure to achieve motor milestones and in death or the need for mechanical ventilation by 2 years of age
in failure to achieve motor milestones and in death or the need forresultsin failure to achieve motor milestones and in death or the need for
to feeding problems as a toddlerledto feeding problems as a toddler
to deathleadingto death
The program(passive) is designedThe program
to the childleadingto the child
to mental retardationledto mental retardation
the family(passive) has been influencedthe family
Every single person(passive) is designedEvery single person
in a high morbidity and mortalityresultingin a high morbidity and mortality
to develop confident , competent , capable , critical , reflective and thoughtful professional early childhood teachers with the ability to apply this knowledge in Aotearoa / New Zealand and international contextsdesignedto develop confident , competent , capable , critical , reflective and thoughtful professional early childhood teachers with the ability to apply this knowledge in Aotearoa / New Zealand and international contexts