0000000000681616

AUTHOR

Tuula Lönnqvist

showing 2 related works from this author

Motor development of infants with univentricular heart at the ages of 16 and 52 weeks

2013

Purpose To compare the motor development of patients with hypoplastic left heart syndrome (HLHS) and other types of univentricular heart (UVH) with peers who are healthy at the ages of 16 and 52 weeks. Methods Motor development was assessed with the Alberta Infant Motor Scale (AIMS). Results Both the 23 patients with HLHS and the 13 patients with UVH had lower total AIMS scores in both observations than the controls. At the age of 52 weeks, patients with HLHS had significantly lower scores in all 4 AIMS subscales, whereas patients with UVH had lower scores only in the prone and standing subscales. Conclusion Motor development of patients with HLHS or UVH is delayed during the first year of …

Heart Defects CongenitalMalePediatricsmedicine.medical_specialtyHeart VentriclesPhysical Therapy Sports Therapy and RehabilitationFirst year of life030204 cardiovascular system & hematologyMotor ActivityNeuropsychological TestsHypoplastic left heart syndrome03 medical and health sciences0302 clinical medicineChild Development030225 pediatricsmedicineHumansProspective StudiesProspective cohort studyMotor skillRetrospective Studiesbusiness.industryInfantRetrospective cohort studyta3141medicine.diseasePrognosisChild developmentUniventricular heartExercise TherapyMotor SkillsChild PreschoolPediatrics Perinatology and Child HealthFemalebusinessPediatric Physical Therapy
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Diagnosis of the neuronal ceroid lipofuscinoses: An update

2006

Abstract For the majority of families affected by one of the neuronal ceroid lipofuscinoses (NCLs), a biochemical and/or genetic diagnosis can be achieved. In an individual case this information not only increases understanding of the condition but also may influence treatment choices and options. The presenting clinical features prompt initial investigation and also guide clinical care. The clinical labels “infantile NCL”, “late infantile NCL” and “juvenile NCL”, therefore remain useful in practice. In unusual or atypical cases ultra-structural analysis of white blood cells or other tissue samples enables planning and prioritisation of biochemical and genetic tests.This review describes cu…

business.industryTreatment choicesAge FactorsVision DisordersInfantNCLBioinformaticsImmunohistochemistryPhenotypeNeuronal Ceroid-LipofuscinosesChild PreschoolDiagnosisMedicineHumansMolecular MedicineClinical careGenetic diagnosisbusinessChildPathologicalMolecular BiologyNeuronal Ceroid-LipofuscinosesBiochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
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