Publication date: Available online 2 February 2017
Source:Pediatric Neurology
Author(s): Soyong Eom, Young-Mock Lee
PurposeLittle is known regarding the neuropsychological profiles of pediatric patients with mitochondrial diseases or their parents, which are crucial for improving quality of life (QOL) for both patients and parents. The present study aimed to delineate neurodevelopment and psychological comorbidity in children with mitochondrial diseases in the preliminary investigation of adequate intervention methods, better prognoses, and improved QOL for both patients and parents.MethodsSeventy children diagnosed with mitochondrial diseases were neuropsychologically evaluated. Neurocognitive (development, intelligence) and psychological (behavior, daily living function, maternal depression, parenting stress) functions were analyzed. Clinical variables including first symptom, epileptic classification, organ involvement, lactic acidosis, brain magnetic resonance imaging findings, muscle pathology, biochemical enzyme assay results, and syndromic diagnosis of mitochondrial diseases were also reviewed.ResultsPre-diagnostic assessments indicated that cognitive and psychomotor development were significantly delayed. Group mean full scale IQ (intelligence quotient) scores indicated mild levels of intellectual disability, borderline levels of verbal IQ impairment, and mild levels of intellectual disability on performance IQ. Many children exhibited clinically significant levels of behavior problems, while mothers of children with mitochondrial diseases exhibited significant increases in parenting stress relative to mothers of healthy children. Furthermore, 65% of mothers exhibited significant levels of depression. Early onset of first symptom, diffuse brain atrophy, and drug-resistant epilepsy negatively influenced neurodevelopmental and adaptive functions.ConclusionBetter understanding of functional levels and profiles of neurodevelopment and psychological comorbidity in children with mitochondrial diseases in the pre-diagnostic period is essential for adequate support and QOL of children with mitochondrial diseases and their parents.
http://ift.tt/2kwBre4
Σφακιανάκης Αλέξανδρος
ΩτοΡινοΛαρυγγολόγος
Αναπαύσεως 5 Άγιος Νικόλαος
Κρήτη 72100
00302841026182
00306932607174
alsfakia@gmail.com
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Κυριακή 5 Φεβρουαρίου 2017
Preliminary Study of Neurodevelopmental Outcomes and Parenting Stress in Pediatric Mitochondrial Disease
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- Higher predictive value of sentinel lymph node bio...
- Peer review: either open it fully or blind it wholly
- Coding and Reimbursement Update for 2017 & Beyond
- Complex traits: Selecting against schooling
- Limb development: a paradigm of gene regulation
- Cutaneous papillary adenocarcinoma in situ
- Reply to “Reappraisal of histopathology of cutaneo...
- Immunomodulation, alemtuzumab associated dermatiti...
- Incidence of Facial Nerve Canal Dehiscence in Prim...
- Incidence of Facial Nerve Canal Dehiscence in Prim...
- The cosmetic and dermatological potential of kerat...
- Comparison of hair removal efficacy and side effec...
- Incidence of Facial Nerve Canal Dehiscence in Prim...
- The cosmetic and dermatological potential of kerat...
- Comparison of hair removal efficacy and side effec...
- Administration of anabolic steroid during adolesce...
- Incidence of Facial Nerve Canal Dehiscence in Prim...
- The breathtaking truth about breath alcohol readin...
- Intraoperative high-dose-rate brachytherapy: An Am...
- Bioengineered three-dimensional diseased intervert...
- The relationship between insulin resistance and pe...
- Top-down HPLC-ESI–MS proteomic analysis of saliva ...
- Expression of odontogenic ameloblast-associated pr...
- Antioxidant capacity of human saliva and periodont...
- Erratum to: Association between heavy metal and me...
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