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8 results on '"Préel, Marie"'

2. Infantile spasmer

Author

Préel, Marie, Møller, Rikke S, Miranda, Maria J, Hoei-Hansen, Christina Engel, Préel, Marie, Møller, Rikke S, Miranda, Maria J, and Hoei-Hansen, Christina Engel

Abstract

Infantile spasms (IS) is a severe developmental and epileptic encephalopathy, occurring mainly in children aged 3-18 months. IS have multiple aetiologies, and the treatment differs accordingly. Early diagnosis and treatment may improve the outcome, but many patients are initially misdiagnosed. Evaluation includes seizure semiology, electroencephalography, cerebral magnetic resonance imaging and genetic and metabolic testing. Treatment varies among centres, and initial treatment may include vigabatrin and/or corticosteroids. In recent years, as summarised in this review, knowledge has substantially increased regarding genetic aetiologies and treatment regimens.

Published
2020

3. Enuresis nocturna hos børn

Author

Préel, Marie, Kamperis, Konstantinos, and Rittig, Søren

Abstract

Nocturnal enuresis is the most common type of urinary incontinence in children. The pathophysiology of the condition is complex with excess nocturnal urine production, bladder reservoir dysfunction and failure to wake up to the sensation of a full bladder, being important elements. The condition can be successfully treated in most children; desmopressin and the enuresis alarm are both effective first-line treatments. Tailoring the treatment based on the clinical characterisation of the patients can improve the outcome.

Published
2018

4. Children with dyskinetic cerebral palsy are severely affected as compared to bilateral spastic cerebral palsy

Author

Préel, Marie, Rackauskaite, Gija, Larsen, Mads Langager, Laursen, Bjarne, Lorentzen, Jakob, Born, Alfred Peter, Langhoff-Roos, Jens, Uldall, Peter, Høi-Hansen, Christina Engel, Préel, Marie, Rackauskaite, Gija, Larsen, Mads Langager, Laursen, Bjarne, Lorentzen, Jakob, Born, Alfred Peter, Langhoff-Roos, Jens, Uldall, Peter, and Høi-Hansen, Christina Engel

Abstract

AIM: We aimed at describing clinical findings in children with dyskinetic as compared to bilateral spastic cerebral palsy (CP).METHODS: Data was extracted from the Danish nationwide CP register. Participants were born in 1999-2007 and were 5-6 years at ascertainment.RESULTS: The total number of CP cases was 1,165 of which 92 had dyskinetic and 540 bilateral spastic CP. Prevalence of dyskinetic CP was 0.16 per 1000 live-births. In participants with dyskinetic compared to bilateral spastic CP, there was more frequently an Apgar level less than five at five minutes (22.7% versus 11.2%) and neonatal seizures (43.5% versus 28.5%), but less respiratory deficiency, hyperbilirubinaemia, and sepsis. Impairment based on gross motor function classification was more severe in dyskinetic CP (level III-V 90.0% versus 66.0%). In dyskinetic CP there was a high rate of reduced developmental quotient (68.1%), visual impairment (39.3%), and epilepsy (51.6%). Basal ganglia lesions were more prevalent in dyskinetic compared to bilateral spastic CP (27.7% vs. 12.8%).CONCLUSION: Cases of dyskinetic CP had overlapping clinical features with cases of bilateral spastic CP, but differed significantly in several perinatal risk factors. The children with dyskinetic CP had experienced more peri- or neonatal adverse events, and neurodevelopmental impairment was severe. This article is protected by copyright. All rights reserved.

Published
2019

7. [Infantile spasms].

Author

Préel M, Møller RS, Miranda MJ, and Hoei-Hansen CE

Subjects
Anticonvulsants therapeutic use, Child, Electroencephalography, Humans, Infant, Magnetic Resonance Imaging, Vigabatrin therapeutic use, Spasms, Infantile diagnosis, Spasms, Infantile drug therapy
Abstract

Infantile spasms (IS) is a severe developmental and epileptic encephalopathy, occurring mainly in children aged 3-18 months. IS have multiple aetiologies, and the treatment differs accordingly. Early diagnosis and treatment may improve the outcome, but many patients are initially misdiagnosed. Evaluation includes seizure semiology, electroencephalography, cerebral magnetic resonance imaging and genetic and metabolic testing. Treatment varies among centres, and initial treatment may include vigabatrin and/or corticosteroids. In recent years, as summarised in this review, knowledge has substantially increased regarding genetic aetiologies and treatment regimens.

Published
2020

8. [Nocturnal enuresis in children].

Author

Préel M, Kamperis K, and Rittig S

Subjects
Child, Deamino Arginine Vasopressin, Humans, Urinary Bladder, Nocturnal Enuresis, Urinary Incontinence
Abstract

Nocturnal enuresis is the most common type of urinary incontinence in children. The pathophysiology of the condition is complex with excess nocturnal urine production, bladder reservoir dysfunction and failure to wake up to the sensation of a full bladder, being important elements. The condition can be successfully treated in most children; desmopressin and the enuresis alarm are both effective first-line treatments. Tailoring the treatment based on the clinical characterisation of the patients can improve the outcome.

Published
2018

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