Prevalence of Sleep Disturbances in Children With Neurofibromatosis Type 1.

Abstract:

:Children with neurodevelopmental disorders are at increased risk for sleep issues, which affect quality of life, cognitive function, and behavior. To determine the prevalence of sleep problems in children with the common neurodevelopmental disorder neurofibromatosis type 1, a cross-sectional study was performed on 129 affected subjects and 89 unaffected siblings, age 2 to 17 years, using the Sleep Disturbance Scale for Children questionnaire. Children with neurofibromatosis type 1 were significantly more likely to have disturbances in initiating and maintaining sleep, arousal, sleep-wake transition, and hyperhidrosis, but not problems with abnormal sleep breathing, or excessive somnolence. Although the overall sleep scores were higher in children with neurofibromatosis type 1, this was not related to a coexisting attention deficit disorder, cognitive impairment, or stimulant medication use. Collectively, these results demonstrate that children with neurofibromatosis type 1 are more likely to have sleep disturbances, and support the use of appropriate interventions for this at-risk population.

journal_name

J Child Neurol

authors

Licis AK,Vallorani A,Gao F,Chen C,Lenox J,Yamada KA,Duntley SP,Gutmann DH

doi

10.1177/0883073813500849

subject

Has Abstract

pub_date

2013-11-01 00:00:00

pages

1400-1405

issue

11

eissn

0883-0738

issn

1708-8283

pii

0883073813500849

journal_volume

28

pub_type

杂志文章
  • Streptococcus oralis as a risk factor for middle cerebral artery thrombosis.

    abstract::We reported a case of an 8-year-old boy who was presented to the emergency department with left-sided hemiparesis. Computed tomography showed hypodense areas in the territory of the right middle cerebral artery, indicating acute cerebral infarct. Diagnostic evaluation was performed to identify the etiology. On the eig...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/08830738050200071401

    authors: Kazanci E,Oguz KK,Gurgey A,Topçu M

    更新日期:2005-07-01 00:00:00

  • Should autistic children be evaluated for mitochondrial disorders?

    abstract::Autism is etiologically heterogeneous; medical conditions are implicated in only a minority of cases, whereas metabolic disorders are even less common. Recently, there have been articles describing the association of autism with mitochondrial abnormalities. We critically review the current literature and conclude that...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/088307380401900510

    authors: Lerman-Sagie T,Leshinsky-Silver E,Watemberg N,Lev D

    更新日期:2004-05-01 00:00:00

  • Ocular motor behavior of children with neurofibromatosis 1.

    abstract::Patients with neurofibromatosis 1 show neurocognitive deficits including abnormal visuospatial performance, but oculomotor behavior has not been studied. We recorded saccades in neurofibromatosis 1 and normal children, ages 6 to 12 years. Patients showed increased latency and diminished amplitude to more eccentric tar...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/08830738030180050301

    authors: Lasker AG,Denckla MB,Zee DS

    更新日期:2003-05-01 00:00:00

  • Valuation of Quality of Life in Pediatric Disability in a Developing Country.

    abstract::This article assessed how Indian providers and mothers value quality of life in pediatric disabilities, hypothesizing lower values with increasing disability, lower values among providers than mothers, and lower values among mothers with versus mothers without a disabled child. We asked 175 participants: "If born tomo...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073818773941

    authors: Spiegel E,Jondhale S,Brajkovic I,Nesbit KC,Allen IE,Bhutani V,Kumar P,Partridge JC

    更新日期:2018-08-01 00:00:00

  • Acute disseminated encephalomyelitis with bilateral thalamic necrosis.

    abstract::Acute disseminated encephalomyelitis is a monophasic inflammatory demyelinating disease of the central nervous system involving the white matter, and to a lesser extent, the gray matter. Bilateral thalamic lesions have been reported in 12% of pediatric patients with acute disseminated encephalomyelitis. In most cases,...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073808331364

    authors: Dardiotis E,Kountra P,Kapsalaki E,Protogerou G,Markopoulou K

    更新日期:2009-08-01 00:00:00

  • Athletic participation after acute ischemic childhood stroke: a survey of pediatric stroke experts.

    abstract::Minimal evidence exists about the risk of recurrent childhood acute ischemic stroke in patients subjected to a subsequent head or neck injury. Recurrent or multiple dissections have been demonstrated in select cases. Minor head trauma has also been associated with acute ischemic stroke. The objective of this study was...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073807306271

    authors: Bernard TJ,deVeber GA,Benke TA

    更新日期:2007-08-01 00:00:00

  • Concussion Alters Dynamic Pupillary Light Responses in Children.

    abstract:AIM:To investigate the impact of concussion on pupillary function in children by examining pupillometric parameters and assessing for differences in children reporting photosensitivity. METHODS:Retrospective chart review was performed of pediatric patients referred for visual symptoms after concussion from 2017 to 201...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073820964040

    authors: Hsu J,Stec M,Ranaivo HR,Srdanovic N,Kurup SP

    更新日期:2021-03-01 00:00:00

  • Children with developmental disabilities in India: age of initial concern and referral for rehabilitation services, and reasons for delay in referral.

    abstract::This study aimed to identify the age at first concern and age at referral for rehabilitation services in children with developmental disabilities in India. Two hundred fifty-nine children were included and data were collected from the parents. In children with developmental disabilities (excluding autism spectrum diso...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073812447685

    authors: Jain R,Juneja M,Sairam S

    更新日期:2013-04-01 00:00:00

  • Neurodevelopmental outcomes in very low-birth-weight infants in Korea: 1998-2007 vs 1989-1997.

    abstract::The authors reviewed the medical records of very low-birth-weight infants admitted from 1998 to 2007 and compared neurodevelopmental outcomes with their previously reported data from 1989 to 1997. The recent group included 824 infants, and the previous group included 471 infants. Neurodevelopmental outcomes were class...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073811408606

    authors: Jang DH,Sung IY,Jeon JY,Moon HJ,Kim KS,Kim EA,Lee BS

    更新日期:2011-11-01 00:00:00

  • Are We Permitting Pediatric Athletes With Sports-Related Concussion to Return to Play Too Soon After Concussion?

    abstract::Current guidelines permitting return to play for athletes who have sustained a concussion rely on resolution of cognitive and physical symptoms. Evolving evidence suggest that vascular, radiologic and cerebral metabolic abnormalities persist in some athletes beyond the period of clinical recovery. This commentary addr...

    journal_title:Journal of child neurology

    pub_type: 社论

    doi:10.1177/0883073818790169

    authors: McAbee GN

    更新日期:2018-10-01 00:00:00

  • Health care needs of children with Tourette syndrome.

    abstract::To document the impact of Tourette syndrome on the health care needs of children and access to health care among youth with Tourette syndrome, parent-reported data from the 2007-2008 National Survey of Children's Health were analyzed. Children with Tourette syndrome had more co-occurring mental disorders than children...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073812465121

    authors: Bitsko RH,Danielson M,King M,Visser SN,Scahill L,Perou R

    更新日期:2013-12-01 00:00:00

  • Episodic migraines in children: limited evidence on preventive pharmacological treatments.

    abstract::The authors conducted a systematic literature review of preventive pharmacological treatments for episodic childhood migraines searching several databases through May 20, 2012. Episodic migraine prevention was examined in 24 publications of randomized controlled trials that enrolled 1578 children in 16 nonrandomized s...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/0883073813488659

    authors: Shamliyan TA,Kane RL,Ramakrishnan R,Taylor FR

    更新日期:2013-10-01 00:00:00

  • The prevalence of neurological disorders in Saudi children: a community-based study.

    abstract::There are limited data on the pattern and prevalence of pediatric chronic neurologic conditions in the region. Therefore, the objective of this study was to establish the prevalence of these disorders in the Kingdom of Saudi Arabia. A multistage probability sampling design was used to select a random sample of Saudi h...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073810371510

    authors: Al Salloum AA,El Mouzan MI,Al Omar AA,Al Herbish AS,Qurashi MM

    更新日期:2011-01-01 00:00:00

  • Hypnagogic behavior disorder: complex motor behaviors during wake-sleep transitions in 2 young children.

    abstract::A nondescribed behavioral disorder was observed during wake-sleep transitions in 2 young children. Two boys had episodes of abnormal behavior in hypnagogic-and occasionally hypnopompic-periods for 1 year from the time they were 1 year and several months old. The episodes consisted of irregular body movements, which co...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073808314964

    authors: Pareja JA,Cuadrado ML,García-Morales I,Gil-Nagel A,Franch O

    更新日期:2008-08-01 00:00:00

  • Diurnal Salivary Cortisol and Regression Status in MECP2 Duplication Syndrome.

    abstract::MECP2 duplication syndrome is an X-linked genomic disorder that is characterized by infantile hypotonia, intellectual disability, and recurrent respiratory infections. Regression affects a subset of individuals, and the etiology of regression has yet to be examined. In this study, alterations in the hypothalamus-pitui...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073815585577

    authors: Peters SU,Byiers BJ,Symons FJ

    更新日期:2016-02-01 00:00:00

  • Congenital blindness, porencephaly, and neonatal thrombocytopenia: a report of four cases.

    abstract::Four unrelated infants with neonatal thrombocytopenia associated with congenital blindness and porencephaly have been seen over an 18-year period. The association of congenital blindness with neonatal thrombocytopenia has not previously been reported. All children had clinical purpura in the neonatal period; in three ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307388800300208

    authors: Manson J,Speed I,Abbott K,Crompton J

    更新日期:1988-04-01 00:00:00

  • Hypertensive encephalopathy in childhood.

    abstract::Hypertensive encephalopathy is an uncommon but recognized complication of malignant hypertension in children. We reviewed the clinical course, laboratory studies, and outcomes of 12 patients with hypertensive encephalopathy seen at the University of Iowa Hospitals and Clinics between 1979 and 1994. The most common pre...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389601100305

    authors: Wright RR,Mathews KD

    更新日期:1996-05-01 00:00:00

  • Pediatric anti-N-methyl-D-aspartate (NMDA) receptor encephalitis: experience of a tertiary care teaching center from north India.

    abstract::Anti-N-methyl-D-aspartate (NMDA) receptor encephalitis is characterized by acute- or subacute-onset encephalopathy with extrapyramidal, psychiatric, and epileptic manifestations. Diagnosis is confirmed by positive antibodies to NMDA receptor in cerebrospinal fluid and serum. Eleven pediatric cases presented over a 2-y...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073813494474

    authors: Chakrabarty B,Tripathi M,Gulati S,Yoganathan S,Pandit AK,Sinha A,Rathi BS

    更新日期:2014-11-01 00:00:00

  • Atypical teratoid/rhabdoid tumor of the spine in a 4-year-old girl.

    abstract::Primary spinal atypical teratoid/rhabdoid tumor is extremely rare. The authors present a case of atypical teratoid/rhabdoid tumor occurring in a 4-year-old girl. Magnetic resonance imaging The authors showed an intramedullary mass extending from the bulbomedullary junction to T1 with leptomeningeal dissemination. The ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073808319319

    authors: Tinsa F,Jallouli M,Douira W,Boubaker A,Kchir N,Hassine DB,Boussetta K,Bousnina S

    更新日期:2008-12-01 00:00:00

  • Hereditary sensory and autonomic neuropathy with autonomic crises: a Turkish variant of familial dysautonomia?

    abstract::Hereditary sensory and autonomic neuropathies have different phenotypes. We report 2 cousins with differing clinical courses of a hereditary sensory and autonomic neuropathy. The progressive disease in case 1 is dominated by loss of sensation, autonomic crises, and pain. Case 2 shows loss of sensation, mental retardat...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073811416664

    authors: Koy A,Freynhagen R,Mayatepek E,Tibussek D

    更新日期:2012-02-01 00:00:00

  • Ataxia with oculomotor apraxia type 1 (AOA1): clinical and neuropsychological features in 2 new patients and differential diagnosis.

    abstract::Ataxia with oculomotor apraxia type 1 (AOA1) is an autosomal recessive disease characterized by early-onset and slowly progressive cerebellar ataxia, areflexia, and peripheral neuropathy. Ocular apraxia is most prominent in the early stage of the disease, by contrast, hypoalbuminemia, hypercholesterolemia, and cogniti...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073808314959

    authors: D'Arrigo S,Riva D,Bulgheroni S,Chiapparini L,Castellotti B,Gellera C,Pantaleoni C

    更新日期:2008-08-01 00:00:00

  • Electron microscopic examination of skin biopsy as a cost-effective tool in the diagnosis of lysosomal storage diseases.

    abstract::In this report, we have summarized our 9-year experience of over 100 proven cases of lysosomal storage disease using electron microscopic evaluation of skin biopsies as a screening tool. The skin biopsy was very specific in establishing the diagnosis in only two disorders, namely neuronal ceroid lipofuscinosis and muc...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389601100408

    authors: Prasad A,Kaye EM,Alroy J

    更新日期:1996-07-01 00:00:00

  • Unilateral auditory neuropathy: case study.

    abstract::This article reports on an 11-year-old boy who was diagnosed with unilateral auditory neuropathy. After failing his annual medical and school hearing screenings, he was referred for audiologic testing, which identified a profound sensorineural hearing loss in his left ear that has remained stable for the past 3 1/2 ye...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380201700415

    authors: Podwall A,Podwall D,Gordon TG,Lamendola P,Gold AP

    更新日期:2002-04-01 00:00:00

  • Morvan syndrome following B-cell lymphoma.

    abstract::Morvan syndrome is a rare autoimmune disease named after the French physician Augustin Marie Morvan. It is characterized by multiple, irregular contractions of the long muscles, weakness, pruritus, hyperhidrosis, insomnia, and delirium. Here, we describe a 17-year-old young man, previously diagnosed with B-cell lympho...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073809356108

    authors: El-Bitar MK,Muwakkit SA,Abboud MR,Sawaya RA,Boustany RM

    更新日期:2010-08-01 00:00:00

  • Are the pupils of premature infants affected by intraventricular hemorrhage?

    abstract::The size and reactivity to light of the pupil in infants with intraventricular hemorrhage has been variously described in the literature. These descriptions have included miosis, reactivity to light, nonreactivity to light, and anisocoria. We studied the size and light reactivity of 20 infants with intraventricular he...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389400900423

    authors: Isenberg SJ,Vazquez M

    更新日期:1994-10-01 00:00:00

  • Gelastic seizure with tectal tumor, lobar holoprosencephaly, and subependymal nodules: clinical report.

    abstract::Gelastic seizures are characterized by inappropriate, stereotyped laughter and are often first recognized when other epileptic manifestations occur. They are frequently associated with hypothalamic hamartomas. Central nervous system developmental abnormalities are rarely reported with gelastic seizures. There is only ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380201700215

    authors: Akman CI,Schubert R,Duran M,Loh J

    更新日期:2002-02-01 00:00:00

  • Neurofibromatosis type 1: magnetic resonance imaging findings.

    abstract::The purpose of this study was to determine the locations and characterize the types of brain abnormalities noted on brain magnetic resonance imaging in patients with probable and definite neurofibromatosis type 1. Patients with definite neurofibromatosis type 1 (n = 17) were studied when clinically indicated, and pati...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389300800105

    authors: DiMario FJ Jr,Ramsby G,Greenstein R,Langshur S,Dunham B

    更新日期:1993-01-01 00:00:00

  • Organizing logopedic therapy for babies with unilateral and bilateral brain lesion in the prespeech period.

    abstract::The goal of the research was to point out the importance of early prespeech therapy for babies suffering from at-birth-acquired unilateral or bilateral lesion in the prespeech period of development. On the basis of existing studies and experience in the field, a protocol and methodology for the observation of the phon...

    journal_title:Journal of child neurology

    pub_type: 临床试验,杂志文章

    doi:10.1177/0883073807299970

    authors: Gec V

    更新日期:2007-01-01 00:00:00

  • The Yield of Neuroimaging in Children Presenting to the Emergency Department With Acute Ataxia in the Post-Varicella Vaccine Era.

    abstract::To determine the yield of neuroimaging in children presenting to the emergency department with acute ataxia in the post-varicella vaccine era, we conducted a cross-sectional study between 1995 and 2013 at a single pediatric tertiary care center. We included children aged 1-18 years evaluated for acute ataxia of <7 day...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073814561300

    authors: Rudloe T,Prabhu SP,Gorman MP,Nigrovic LE,Harper MB,Landschaft A,Kimia AA

    更新日期:2015-09-01 00:00:00

  • Effects of Developmental Age on Symptom Reporting and Neurocognitive Performance in Youth After Sports-Related Concussion Compared to Control Athletes.

    abstract::There is increased necessity to focus research on school-aged athletes with sports-related concussion (SRC). This study assessed differences in symptom reporting and neurocognitive performance in youth athletes who sustained a sports-related concussion. A total of 1345 concussed and 3529 nonconcussed athletes (ages 8-...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073818766815

    authors: Murdaugh DL,Ono KE,Morris SO,Burns TG

    更新日期:2018-06-01 00:00:00