Risk of cerebral palsy in relation to pregnancy disorders and preterm birth: a national cohort study.

Abstract:

AIM:To assess the risk of developing cerebral palsy in relation to pregnancy disorders and preterm birth. METHOD:By linking the Medical Birth Registry of Norway to other national registries, we identified all live births in Norway from 1967 through to 2001. Risks of cerebral palsy (CP) after preterm delivery and pregnancy disorders were estimated in different gestational age groups. RESULT:In total, 1 764 509 children delivered at 23 to 43 weeks' gestation were included. The prevalence of CP was 1.8 per 1000 births. Absolute risk of CP was 8.5% among children born at 23 to 27 weeks' gestation, 5.6% at 28 to 30 weeks, 2.0% at 31 to 33 weeks, 0.4% at 34 to 36 weeks, and 0.1% thereafter. Placental abruption, chorioamnionitis, prolonged rupture of membranes, intrauterine growth restriction, pre-eclampsia, multiple births, placenta previa, bleeding, cervical conization, and congenital malformation were all associated with CP. Before 32 weeks' gestation, absolute risk of CP was highest with chorioamnionitis (9.1%) and lowest with pre-eclampsia (3.1%). Among those born after 31 weeks, the absolute risk of CP was more consistently (but also more slightly) increased with a recorded pregnancy disorder. INTERPRETATION:Early delivery and pregnancy disorders were both strong risk factors for CP. The added risks with recorded pregnancy disorders varied within categories of gestational age.

journal_name

Dev Med Child Neurol

authors

Trønnes H,Wilcox AJ,Lie RT,Markestad T,Moster D

doi

10.1111/dmcn.12430

subject

Has Abstract

pub_date

2014-08-01 00:00:00

pages

779-85

issue

8

eissn

0012-1622

issn

1469-8749

journal_volume

56

pub_type

杂志文章
  • Cognitive impairment in children with CACNA1A mutations.

    abstract:AIM:To describe the clinico-radiological phenotype of children with a CACNA1A mutation and to precisely evaluate their learning ability and cognitive status. METHOD:Children between the ages of 3 and 18 years harboring a pathogenic CACNA1A mutation associated with episodic ataxia, hemiplegic migraine, benign paroxysma...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/dmcn.14261

    authors: Humbertclaude V,Riant F,Krams B,Zimmermann V,Nagot N,Annequin D,Echenne B,Tournier-Lasserve E,Roubertie A,Episodic Syndrome Consortium.

    更新日期:2020-03-01 00:00:00

  • Communication ability and communication methods in children with cerebral palsy.

    abstract:AIM:To investigate if communication ability and method were related to each other and to age, sex, gross motor function, or manual ability in children with cerebral palsy. METHOD:This cross-sectional study used data registered in the Swedish Cerebral Palsy Surveillance Program registry, involving 3000 children aged 0 ...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/dmcn.14546

    authors: Kristoffersson E,Dahlgren Sandberg A,Holck P

    更新日期:2020-08-01 00:00:00

  • The medical examination of children on entry to school. The results and use of neurodevelopmental assessment.

    abstract::In the North Paddington Primary School Study 350 children were identified at five and studied over a five-year period. The children were given a comprehensive examination on entry to school, the findings from which are briefly described. Here the results of the neurodevelopmental assessment are reviewed. Children with...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/j.1469-8749.1987.tb02106.x

    authors: Bax M,Whitmore K

    更新日期:1987-02-01 00:00:00

  • The septum pellucidum and spatial ability of children with optic nerve hypoplasia.

    abstract::Animal studies suggest that spatial skills are dependent on an intact septum pellucidum. This theory was tested by comparing patients who were visually impaired due to bilateral optic nerve hypoplasia: 13 with a septum pellucidum were compared with six children without a septum pellucidum. There was no difference in s...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/j.1469-8749.1994.tb11832.x

    authors: Groenveld M,Pohl KR,Espezel H,Jan JE

    更新日期:1994-03-01 00:00:00

  • Independent role of neonatal seizures in subsequent neurological outcomes: a population-based study.

    abstract:AIM:This population-based study aimed to estimate the impact of neonatal seizures on subsequent neurological outcomes, regardless of underlying etiology. METHOD:We performed a retrospective cohort study (1st January 2009-31st December 2014), using a USA nationwide claims database. Newborn infants enrolled in 2009 were...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/dmcn.14174

    authors: Oh A,Thurman DJ,Kim H

    更新日期:2019-06-01 00:00:00

  • Mild developmental delay due to ring chromosome 19 mosaicism.

    abstract::Children with mild developmental delay without dysmorphic features do not often have identifiable underlying aetiological factors. We report on a 5-year-old girl with mild developmental delay and dysmorphic features which were previously unrecognized. She was found to have supernumerary ring chromosome 19 mosaicism wh...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1017/s0012162299000092

    authors: Vaz I,Larkins SA,Norman A,Green SH

    更新日期:1999-01-01 00:00:00

  • Cognitive functioning in Lesch-Nyhan syndrome: a 4-year follow-up study.

    abstract::Lesch-Nyhan syndrome (LNS) is a rare disorder of metabolism caused by a defective gene on the X chromosome. It is typically characterized by choreoathetosis, hypertonia, hyperreflexia, and self-mutilation. The present study is a 4-year follow-up investigation of the cognitive status of six subjects with a mean age of ...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1017/s0012162299000547

    authors: Matthews WS,Solan A,Barabas G,Robey K

    更新日期:1999-04-01 00:00:00

  • Association between rates of premature delivery and intra-uterine growth retardation.

    abstract::It has been suggested that there is a positive epidemiological correlation between the rates of premature delivery and intra-uterine growth retardation. This was tested across three series of live births, cross-classified according to gravidity and mother's age in two states, North Carolina (caucasians and blacks), an...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/j.1469-8749.1982.tb13701.x

    authors: Spiers PS,Wacholder S

    更新日期:1982-12-01 00:00:00

  • Psychometric properties of functional mobility tools in hereditary spastic paraplegia and other childhood neurological conditions.

    abstract:AIM:To evaluate studies on the psychometric properties of measurement tools used to quantify functional mobility in children with hereditary spastic paraplegia (HSP) and other childhood neurological conditions. METHOD:Two independent reviewers identified measures previously used by clinicians to quantify functional mo...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章,评审

    doi:10.1111/j.1469-8749.2012.04284.x

    authors: Adair B,Said CM,Rodda J,Morris ME

    更新日期:2012-07-01 00:00:00

  • Handedness and progressive hydrocephalus in spina bifida patients.

    abstract::Hand preference and functional hand-dominance of 45 spina bifida patients (aged 13 to 25 years) were assessed by means of self-reports on an ordinal scale and a tapping task. Non-right-handedness was more frequent among patients with accompanying progressive hydrocephalus. Left-hand preference was significantly more f...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/j.1469-8749.1993.tb11730.x

    authors: Wassing HE,Siebelink BM,Luyendijk W

    更新日期:1993-09-01 00:00:00

  • Long-term outcome of vein of Galen malformation.

    abstract:AIM:To describe the long-term outcomes of children by the time they reached school age with vein of Galen aneurysmal malformation (VGAM). METHOD:This was a retrospective observational study on a consecutive cohort of patients with VGAM. We included patients with at least one Francophone parent, aged between 6 and 11 y...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/dmcn.14392

    authors: Taffin H,Maurey H,Ozanne A,Durand P,Husson B,Knebel JF,Adamsbaum C,Deiva K,Saliou G

    更新日期:2020-06-01 00:00:00

  • MRI brain changes in subjects with Down syndrome with and without dementia.

    abstract::Individuals with Down syndrome (DS), a disorder of known genetic etiology (trisomy of chromosome 21), exhibit several types of structural brain abnormalities that are detectable pathologically and by MRI. In addition, in middle age, individuals with DS develop histological and, in some cases, clinical features of Alzh...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:

    authors: Pearlson GD,Breiter SN,Aylward EH,Warren AC,Grygorcewicz M,Frangou S,Barta PE,Pulsifer MB

    更新日期:1998-05-01 00:00:00

  • Diagnostic yield and treatment impact of whole-genome sequencing in paediatric neurological disorders.

    abstract:AIM:To investigate the diagnostic yield and treatment impact of whole-genome sequencing (WGS) in patients with paediatric neurological disorders. METHOD:From January 2016 to December 2019, paediatric patients who had suspected genetic neurological disorders were assessed using WGS. The phenotypes of eligible patients ...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/dmcn.14722

    authors: Lee HF,Chi CS,Tsai CR

    更新日期:2020-11-26 00:00:00

  • Tactile sensory abilities in cerebral palsy: deficits in roughness and object discrimination.

    abstract::Motor deficits in cerebral palsy (CP) have been well documented; however, associated sensory impairment in CP remains poorly understood. We examined tactile object recognition in the hands using geometric shapes, common objects, and capital letters. Discrimination of tactile roughness was tested using paired horizonta...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/j.1469-8749.2008.03105.x

    authors: Wingert JR,Burton H,Sinclair RJ,Brunstrom JE,Damiano DL

    更新日期:2008-11-01 00:00:00

  • Late sequelae of low birthweight: mediators of poor school performance at 11 years.

    abstract::This study examined the effect of low birthweight on school achievement and the mediating roles of cognitive and behavioural factors. The sample (115 females, 100 males) was selected from a longitudinal study of first-born singleton children, born between 1986 and 1988 of German-speaking parents, recruited from eight ...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1017/s0012162203000860

    authors: Weindrich D,Jennen-Steinmetz C,Laucht M,Schmidt MH

    更新日期:2003-07-01 00:00:00

  • Changes to medial gastrocnemius architecture after surgical intervention in spastic diplegia.

    abstract::We assessed the architecture of the medial gastrocnemius in nine children (five males, four females; age range 6 to 15 years; mean 10 years 10 months, SD 3 years 6 months) with spastic diplegia by ultrasound imaging before and after a gastrocnemius recession. The children were ambulant (seven independent, one with a p...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1017/s0012162204001124

    authors: Shortland AP,Fry NR,Eve LC,Gough M

    更新日期:2004-10-01 00:00:00

  • Elementary visuospatial perception deficit in children with neurodevelopmental disorders.

    abstract:AIM:To assess the prevalence of elementary visuospatial perception (EVSP) deficit in children with neurodevelopmental disorders. METHOD:Using a screening test designed and validated to measure dorsal EVSP ability, 168 children (122 males, 46 females; mean age 10y [SD 1y 10mo], range 4y 8mo-16y 4mo) diagnosed with deve...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/dmcn.14743

    authors: Pisella L,Vialatte A,Martel M,Prost-Lefebvre M,Caton MC,Stalder M,Yssad R,Roy AC,Vuillerot C,Gonzalez-Monge S

    更新日期:2020-12-11 00:00:00

  • Interventions and lower-limb macroscopic muscle morphology in children with spastic cerebral palsy: a scoping review.

    abstract:AIM:To identify and map studies that have assessed the effect of interventions on lower-limb macroscopic muscle-tendon morphology in children with spastic cerebral palsy (CP). METHOD:We conducted a literature search of studies that included pre- and post-treatment measurements of lower-limb macroscopic muscle-tendon m...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章,评审

    doi:10.1111/dmcn.14652

    authors: Walhain F,Desloovere K,Declerck M,Van Campenhout A,Bar-On L

    更新日期:2020-09-02 00:00:00

  • Short-latency somatosensory evoked potentials in infantile autism: evidence of hyperactivity in the right primary somatosensory area.

    abstract::Children with infantile autism sometimes show hyperesthesia or hypoesthesia to touch, pain, and/or temperature. To clarify the pathophysiology, we examined short-latency somatosensory evoked potentials (S-SEPs), elicited by median nerve stimulation, in 24 children with infantile autism (17 males, seven females; age ra...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1017/s0012162207000059.x

    authors: Miyazaki M,Fujii E,Saijo T,Mori K,Hashimoto T,Kagami S,Kuroda Y

    更新日期:2007-01-01 00:00:00

  • Development of motor co-ordination by normal left-handed children.

    abstract::Ninety-six normal left-handed children were tested for motor co-ordination on a series of timed repetitive tasks, alternating left and right hands, feet and fingers. Preferred hand advantage could be demonstrated to the same degree for the left hand of these children as it had been for the preferred right hand in prev...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/j.1469-8749.1984.tb04414.x

    authors: Rudel RG,Healey J,Denckla MB

    更新日期:1984-02-01 00:00:00

  • Social impairments in alternating hemiplegia of childhood.

    abstract:AIM:To evaluate presence and severity of social impairments in alternating hemiplegia of childhood (AHC) and determine factors that are associated with social impairments. METHOD:This was a retrospective analysis of 34 consecutive patients with AHC (19 females, 15 males; mean age: 9y 7mo, SD 8y 2mo, range 2y 7mo-40y),...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/dmcn.14473

    authors: Uchitel J,Abdelnour E,Boggs A,Prange L,Pratt M,Bonner M,Jasien J,Dawson G,Abrahamsen T,Mikati MA

    更新日期:2020-07-01 00:00:00

  • The efficacy of functional gait training in children and young adults with cerebral palsy: a systematic review and meta-analysis.

    abstract:AIM:The aim of this systematic review was to investigate the effects of functional gait training on walking ability in children and young adults with cerebral palsy (CP). METHOD:The review was conducted using standardized methodology, searching four electronic databases (PubMed, Embase, CINAHL, Web of Science) for rel...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章,meta分析,评审

    doi:10.1111/dmcn.13708

    authors: Booth ATC,Buizer AI,Meyns P,Oude Lansink ILB,Steenbrink F,van der Krogt MM

    更新日期:2018-09-01 00:00:00

  • Regional cerebral blood flow in weight-restored anorexia nervosa: a preliminary study.

    abstract::Twenty-one individuals (19 females, two males) with teenage-onset anorexia nervosa (AN), 19 of whom were weight restored, were assessed using single-photon emission computed tomography (SPECT) 7 years after onset of AN, at a mean age of 22 years. For comparison we recruited a younger group without neuropsychiatric dis...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1017/s0012162201000457

    authors: Råstam M,Bjure J,Vestergren E,Uvebrant P,Gillberg IC,Wentz E,Gillberg C

    更新日期:2001-04-01 00:00:00

  • Outcome at school age of children with birthweights of 1000 grams or less.

    abstract::A follow-up study was done of extremely low-birthweight infants (less than or equal to 1000g) born between 1976 and 1979, a period when aggressive intervention was not routine practice. The survival rate was 19 per cent. 44 of the 46 survivors were followed to a mean age of 6 1/2 years. By five years of age 23 of the ...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/j.1469-8749.1988.tb04748.x

    authors: Lefebvre F,Bard H,Veilleux A,Martel C

    更新日期:1988-04-01 00:00:00

  • Acute dystonic reaction to bethanechol--a direct acetylcholine receptor agonist.

    abstract::Bethanechol is a direct agonist of the acetylcholine receptor that was recently introduced in the therapy of gastro-oesophageal reflux. Acute dystonic reactions to bethanechol were observed in a 10-month-old infant who also demonstrated similar dystonic reactions to dopamine receptor blocking agents of two different c...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/j.1469-8749.1986.tb03909.x

    authors: Shafrir Y,Levy Y,Beharab A,Nitzam M,Steinherz R

    更新日期:1986-10-01 00:00:00

  • Pacinioma of the cauda equina.

    abstract::Lesions composed of Pacinian corpuscles or showing Pacinian corpuscle differentiation have usually been described in relation to benign tumours of the peripheral nervous system or reactive hyperplastic processes. On the other hand, mature Pacinian corpuscles have occasionally been detected as part of intraspinal lumbo...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1017/S0012162206002180

    authors: Kojc N,Korsic M,Popovic M

    更新日期:2006-12-01 00:00:00

  • A previously undescribed leukodystrophy in Leigh syndrome associated with T9176C mutation of the mitochondrial ATPase 6 gene.

    abstract::We report two male Taiwanese siblings in whom the T-->C point mutation at nucleotide 9176 of the mitochondrial ATPase 6 gene (m.9176T>C mutation) was associated with early onset hypotonia, lactic acidosis, and death due to respiratory arrest at 7 and 10 months old. Brain MRI showed lesions over diffuse white matter an...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1017/s0012162207000163.x

    authors: Hung PC,Wang HS

    更新日期:2007-01-01 00:00:00

  • Arthrogryposis multiplex congenita, AD 1156.

    abstract::A case of arthrogryposis multiplex congenita in an eight-year-old girl was recounted by Thomas of Monmouth in a mid twelfth-century English hagiographic narrative, The Life and Miracles of St William of Norwich. The child had deformities of both hands and both feet at birth, and she developed torticollis and probably ...

    journal_title:Developmental medicine and child neurology

    pub_type: 历史文章,杂志文章

    doi:10.1111/j.1469-8749.1996.tb15036.x

    authors: Gordon EC

    更新日期:1996-01-01 00:00:00

  • Early prognosis for ambulation of neonatal intensive care survivors with cerebral palsy.

    abstract::The ambulatory status of 74 neonatal intensive care unit survivors with cerebral palsy, excluding those with central nervous system malformations and syndromes, was assessed at eight years of age. Detailed examinations were completed at two and eight years of age; of the 47 who were sitting by two years, 46 became amb...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/j.1469-8749.1989.tb04072.x

    authors: Watt JM,Robertson CM,Grace MG

    更新日期:1989-12-01 00:00:00

  • Epilepsy in very preterm infants: neonatal cranial ultrasound reveals a high-risk subcategory.

    abstract::The aim of this study was to investigate the association between epilepsy and perinatal brain injury in a cohort of 610 infants born preterm at <33 weeks' gestation. The prevalence of epilepsy in this cohort was 4.3% as determined by a postal questionnaire survey. Most children with epilepsy (16 of 24) had high-risk c...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/j.1469-8749.1998.tb12339.x

    authors: Amess PN,Baudin J,Townsend J,Meek J,Roth SC,Neville BG,Wyatt JS,Stewart A

    更新日期:1998-11-01 00:00:00