Childhood subdural hemorrhage, macrocephaly, and coagulopathy associated with Prader-Willi syndrome: case report and review of the literature.

Abstract:

:A 16-month-old girl with a history of Prader-Willi syndrome and progressive macrocephaly manifested large, bilateral, subdural hemorrhages of differing ages on magnetic resonance imaging. Subsequent evaluation revealed a deficiency of von Willebrand factor, but after repeated evaluations, no conclusive evidence of nonaccidental trauma became apparent. Subdural hemorrhages of varying ages are frequently associated with nonaccidental trauma during early childhood. However, several uncommon conditions may present as subdural hemorrhages and thus mimic nonaccidental trauma. Our patient demonstrates a combination of Prader-Willi syndrome, von Willebrand factor deficiency, and enlargement of the extra-axial spaces. All of these in isolation were associated with subdural hemorrhages. We review the scant literature on subdural hemorrhages in Prader-Willi syndrome and other conditions that mimic nonaccidental trauma.

journal_name

Pediatr Neurol

journal_title

Pediatric neurology

authors

Carr RB,Khanna PC,Saneto RP

doi

10.1016/j.pediatrneurol.2012.03.011

subject

Has Abstract

pub_date

2012-07-01 00:00:00

pages

59-61

issue

1

eissn

0887-8994

issn

1873-5150

pii

S0887-8994(12)00123-3

journal_volume

47

pub_type

杂志文章,评审
  • Overstimulation of nerve growth factors in postinfectious and autoimmune diseases.

    abstract::Nerve growth factor (NGF) in cerebrospinal fluid was measured by ELISA in ten children with postinfectious diseases and in five children with diseases suggested to be of autoimmune etiology. Three groups of patients were studied: (1) those with moderately elevated concentrations (50.67 +/- 17.02 pg/mL, mean and SEM), ...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(97)00204-x

    authors: Riikonen RS,Söderström S,Korhonen LT,Lindholm DB

    更新日期:1998-03-01 00:00:00

  • Infant Motor Delay and Early Symptomatic Syndromes Eliciting Neurodevelopmental Clinical Examinations in Japan.

    abstract:BACKGROUND:Abnormalities of early motor development have been reported in autism spectrum disorder, attention-deficit/hyperactivity disorder, intellectual developmental disorder, developmental coordination disorder, and other Early Symptomatic Syndromes Eliciting Neurodevelopmental Clinical Examinations (ESSENCE). Howe...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/j.pediatrneurol.2015.09.008

    authors: Hatakenaka Y,Kotani H,Yasumitsu-Lovell K,Suzuki K,Fernell E,Gillberg C

    更新日期:2016-01-01 00:00:00

  • West syndrome following deep hypothermic infant cardiac surgery.

    abstract::Postoperative seizures are among the more common complications of cardiac surgery in children. These seizures have traditionally been considered benign, transient phenomena with little, if any, prognostic significance. We report 4 infants with early postoperative seizures following cardiac surgery who later developed ...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/0887-8994(94)90111-2

    authors: du Plessis AJ,Kramer U,Jonas RA,Wessel DL,Riviello JJ

    更新日期:1994-10-01 00:00:00

  • Neonatal posthemorrhagic hydrocephalus: neuropathologic and immunohistochemical studies.

    abstract::A neuropathologic study was undertaken to examine associated brain damage in patients with fetal and neonatal posthemorrhagic hydrocephalus (PHH). In PHH the association of periventricular leukomalacia and pontosubicular necrosis was not increased, but that of cerebellar subarachnoid hemorrhage and olivo-cerebellar pa...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/0887-8994(95)00183-g

    authors: Fukumizu M,Takashima S,Becker LE

    更新日期:1995-10-01 00:00:00

  • Pediatric cefepime neurotoxicity.

    abstract::Cefepime toxicity is characterized by altered mental status, confusion, and decreased responsiveness. We describe a 14-year-old girl who developed acute encephalopathy associated with supratherapeutic cefepime concentrations in the setting of acute renal failure. The authors were unable to identify any previous report...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/j.pediatrneurol.2012.08.017

    authors: Landgrave LC,Lock JL,Whitmore JM,Belcher CE

    更新日期:2012-12-01 00:00:00

  • Pediatric Hirayama disease.

    abstract::We report on a 16-year-old girl with muscular atrophy of a distal upper extremity (Hirayama disease). The disease progressed insidiously, and during our first examination, she exhibited weakness and wasting in the right hand, accompanied by cold paresis. No sensory disturbance was evident. A nerve conduction test reve...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/j.pediatrneurol.2010.03.015

    authors: Hosokawa T,Fujieda M,Wakiguchi H,Oosaki Y

    更新日期:2010-08-01 00:00:00

  • Cerebrovascular Complications of Pediatric Blunt Trauma.

    abstract::Ischemic and hemorrhagic stroke can occur in the setting of pediatric trauma, particularly those with head or neck injuries. The risk of stroke appears highest within the first two weeks after trauma. Stroke diagnosis may be challenging due to lack of awareness or concurrent injuries limiting detailed neurological ass...

    journal_title:Pediatric neurology

    pub_type: 杂志文章,评审

    doi:10.1016/j.pediatrneurol.2019.12.009

    authors: Galardi MM,Strahle JM,Skidmore A,Kansagra AP,Guilliams KP

    更新日期:2020-07-01 00:00:00

  • Narcolepsy with cataplexy as presenting symptom of occult neuroblastoma.

    abstract::Neuroblastoma associated with the paraneoplastic syndrome of opsoclonus-myoclonus is well-described. However, presentation with narcolepsy-cataplexy is not well-documented in the literature. Narcolepsy with cataplexy is also rare in children younger than 5 years of age. Here we describe three patients, each presenting...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/j.pediatrneurol.2012.12.038

    authors: Sinsioco C,Silver K,Forrest KM,Gray J,Nechay A,Sheldon S,Chelmicka Schorr E

    更新日期:2013-07-01 00:00:00

  • The Communication Function Classification System: cultural adaptation, validity, and reliability of the Farsi version for patients with cerebral palsy.

    abstract:BACKGROUND:This study developed a Farsi language Communication Function Classification System and then tested its reliability and validity. METHODS:Communication Function Classification System is designed to classify the communication functions of individuals with cerebral palsy. Up until now, there has been no instru...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/j.pediatrneurol.2014.10.026

    authors: Soleymani Z,Joveini G,Baghestani AR

    更新日期:2015-03-01 00:00:00

  • Predicting neuropsychologic outcome after traumatic brain injury in children.

    abstract::The ability to predict long-term neurologic and neuropsychologic outcomes in 22 children, ages 1 week to 14 years at the time of traumatic brain injury, was investigated using proton magnetic resonance spectroscopy acquired post injury and compared with standardized neurologic, intellectual, and neuropsychologic testi...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(02)00491-5

    authors: Brenner T,Freier MC,Holshouser BA,Burley T,Ashwal S

    更新日期:2003-02-01 00:00:00

  • Discontinuation of medications after successful epilepsy surgery in children.

    abstract::To evaluate the need for antiepileptic drugs after successful epilepsy surgery in pediatric patients, we retrospectively reviewed patients who had epilepsy surgery and were seizure free or had rare nondisabling auras during the first 6 postoperative months. Association between drug discontinuation and seizure recurren...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/j.pediatrneurol.2008.01.010

    authors: Lachhwani DK,Loddenkemper T,Holland KD,Kotagal P,Mascha E,Bingaman W,Wyllie E

    更新日期:2008-05-01 00:00:00

  • Sarcolemmal alpha and gamma sarcoglycan protein deficiencies in Turkish siblings with a novel missense mutation in the alpha sarcoglycan gene.

    abstract:BACKGROUND:The sarcoglycan alpha gene, also known as the adhalin gene, is located on chromosome 17q21; mutations in this gene are associated with limb-girdle muscular dystrophy type 2D. We describe two Turkish siblings with findings consistent with limb-girdle muscular dystrophy type 2D. The evaluation excluded a dystr...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/j.pediatrneurol.2013.12.024

    authors: Diniz G,Tosun Yildirim H,Akinci G,Hazan F,Ozturk A,Yararbas K,Tukun A

    更新日期:2014-06-01 00:00:00

  • A proposed new method for electroencephalography trace recording in children younger than two years: an observational study.

    abstract::Epilepsy is a common disorder in pediatric neurology, and electroencephalography (EEG) continues to play an important role in its diagnosis. However, the small size of a child's head and immaturity of the brain make EEG interpretation more difficult in children than in adults. This article presents a new method of EEG...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/j.pediatrneurol.2013.01.009

    authors: Nikkhah K,Shoeibi A,Hasanpour M

    更新日期:2013-06-01 00:00:00

  • Computed tomography and magnetic resonance imaging in late-onset globoid cell leukodystrophy (Krabbe disease).

    abstract::A five-year-old white male presented with a history of progressive loss of vision that was subsequently followed by progressive corticospinal dysfunction. Evaluation revealed the presence of leukodystrophy which was confirmed by a deficiency of the enzyme, galactosylceramide beta-galactosidase. We present the clinical...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(85)80009-6

    authors: Brownsworth RD,Bodensteiner JB,Schaefer GB,Barnes P

    更新日期:1985-07-01 00:00:00

  • Vitamins ameliorate secondary mitochondrial failure in neonatal rat brain.

    abstract::Recirculation after transient intrauterine ischemia has previously been found to be accompanied by secondary mitochondrial dysfunction in the immature rat brain. This study was performed to assess the efficacy of combined treatment with ascorbic acid and alpha-tocopherol in improving secondary brain damage. On the 17t...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(02)00383-1

    authors: Nakai A,Shibazaki Y,Taniuchi Y,Oya A,Asakura H,Koshino T,Araki T

    更新日期:2002-07-01 00:00:00

  • Toxicity of Salvia officinalis in a newborn and a child: an alarming report.

    abstract::Although it is widely believed that herbal products are beneficial to the health, some herbal products can result in serious adverse effects, such as epileptic seizures, especially in children who are particularly susceptible. Sage oil contains well-known convulsant substances such as thujone, camphor, and cineole in ...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/j.pediatrneurol.2011.05.012

    authors: Halicioglu O,Astarcioglu G,Yaprak I,Aydinlioglu H

    更新日期:2011-10-01 00:00:00

  • Benign paroxysmal torticollis in infancy.

    abstract::Benign paroxysmal torticollis in infancy is characterized by periods of torticollic posturing of the head. The onset of the episodes usually occurs during the first month of life and may recur at varying intervals until the age of 1-5 years. This appears to be a self-limited disorder. The follow-up of 7 patients with ...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/0887-8994(93)90031-7

    authors: Cohen HA,Nussinovitch M,Ashkenasi A,Straussberg R,Kauschanksy A,Frydman M

    更新日期:1993-11-01 00:00:00

  • Laterality of brain and ocular lesions in Aicardi syndrome.

    abstract::This study reports a large case series of children with Aicardi syndrome. A new severity scoring system is established to assess sidedness of ocular and brain lesions. Thirty-five children were recruited from Aicardi syndrome family conferences. All children received dilated ophthalmologic examinations, and brain magn...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/j.pediatrneurol.2011.04.007

    authors: Cabrera MT,Winn BJ,Porco T,Strominger Z,Barkovich AJ,Hoyt CS,Wakahiro M,Sherr EH

    更新日期:2011-09-01 00:00:00

  • Neurological Manifestations of Medical Child Abuse.

    abstract:BACKGROUND:Medical child abuse occurs when a child receives unnecessary and harmful, or potentially harmful, medical care at the instigation of a caretaker through exaggeration, falsification, or induction of symptoms of illness in a child. Neurological manifestations are common with this type of maltreatment. OBJECTI...

    journal_title:Pediatric neurology

    pub_type: 杂志文章,评审

    doi:10.1016/j.pediatrneurol.2015.09.010

    authors: Doughty K,Rood C,Patel A,Thackeray JD,Brink FW

    更新日期:2016-01-01 00:00:00

  • Alexia without agraphia following biopsy of a left thalamic tumor.

    abstract::Alexia without agraphia is a rare disconnection syndrome characterized by the loss of reading ability with retention of writing and verbal comprehension. We report a patient who developed alexia without agraphia after undergoing a biopsy for a malignant glioma involving the left thalamus. A 15-year-old right-handed ma...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/S0887-8994(03)00417-X

    authors: Tamhankar MA,Coslett HB,Fisher MJ,Sutton LN,Liu GT

    更新日期:2004-02-01 00:00:00

  • A young infant with musicogenic epilepsy.

    abstract::Musicogenic epilepsy is a relatively rare form of epilepsy. In its pure form, it is characterized by epileptic seizures that are provoked exclusively by listening to music. The usual type of seizure is partial complex or generalized tonic-clonic. Precipitating factors are quite specific, such as listening to only one ...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(03)00011-0

    authors: Lin KL,Wang HS,Kao PF

    更新日期:2003-05-01 00:00:00

  • Favorable Outcomes With Early Interleukin 6 Receptor Blockade in Severe Acute Necrotizing Encephalopathy of Childhood.

    abstract:BACKGROUND:Outcome in severe acute necrotizing encephalopathy of childhood is poor, with high mortality (30%) and moderate to severe disability in survivors despite the use of intravenous corticosteroids or immunoglobulins. Increased blood interleukin 6 level correlates with poor outcome. METHODS:We report the early u...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/j.pediatrneurol.2019.04.009

    authors: Koh JC,Murugasu A,Krishnappa J,Thomas T

    更新日期:2019-09-01 00:00:00

  • Fetal neurologic consultations.

    abstract::The pediatric neurologist can fulfill a useful role as a subspecialty consultant concerning the fetus with a suspected brain disorder, given that neurologic disease may occur before the intrapartum period. Brain disorders detected in the neonatal period may also reflect fetal brain damage before dysfunction is first d...

    journal_title:Pediatric neurology

    pub_type: 杂志文章,评审

    doi:10.1016/s0887-8994(03)00234-0

    authors: Scher MS

    更新日期:2003-09-01 00:00:00

  • Acute disseminated encephalomyelitis after Japanese B encephalitis vaccination.

    abstract::A 6-year-old girl (Patient 1) and a 5-year-old boy (Patient 2) with acute disseminated encephalomyelitis after Japanese B encephalitis vaccination are reported. Drowsiness, paresthesias, and gait disturbance were observed at 14 days (Patient 1) and 17 days (Patient 2) after the vaccination; however, transient impairme...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/0887-8994(92)90036-x

    authors: Ohtaki E,Murakami Y,Komori H,Yamashita Y,Matsuishi T

    更新日期:1992-03-01 00:00:00

  • Life expectancy of children with cerebral palsy.

    abstract::Risk factors for mortality of young children with cerebral palsy were studied using a sample of 12,709 children aged 0.5-3.5 years with cerebral palsy who had received services from the State of California between 1980 and 1995. The most powerful prognostic factors for survival were simple functional items: mobility a...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(97)00172-0

    authors: Strauss DJ,Shavelle RM,Anderson TW

    更新日期:1998-02-01 00:00:00

  • Dendritic and synaptic pathology in mental retardation.

    abstract::Histologic changes in brains from mentally retarded patients are often subtle and may be limited to abnormalities in the dendritic and synaptic organization of the cerebral cortex. Special methods may be necessary for their demonstration. This review summarizes data on dendritic and synaptic pathology in human mental ...

    journal_title:Pediatric neurology

    pub_type: 杂志文章,评审

    doi:10.1016/0887-8994(91)90001-2

    authors: Huttenlocher PR

    更新日期:1991-03-01 00:00:00

  • Muscle pathology and clinical features of the sarcolemmopathies.

    abstract::We report the clinical features and the muscle pathology in 2 patients with congenital muscular dystrophy (CMD) secondary to merosin deficiency and in 2 patients with sarcoglycan (adhalin) deficiency. Electron microscopic examination revealed sarcolemmal defects in non-necrotic muscle fibers in all cases. These pathol...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(96)00265-2

    authors: Fadic R,Waclawik AJ,Lewandoski PJ,Lotz BP

    更新日期:1997-01-01 00:00:00

  • Pediatric tumefactive demyelination: case series and review of the literature.

    abstract::Tumefactive demyelinating lesions may be misdiagnosed as brain neoplasms or abscesses. In this paper, we present four cases of pediatric tumefactive demyelination. Twelve cases of pediatric tumefactive demyelination previously reported in the English literature are also summarized. We describe the neuroimaging charact...

    journal_title:Pediatric neurology

    pub_type: 杂志文章,评审

    doi:10.1016/s0887-8994(01)00322-8

    authors: McAdam LC,Blaser SI,Banwell BL

    更新日期:2002-01-01 00:00:00

  • Central nervous system vasculopathy associated with neonatal lupus.

    abstract::Neonatal lupus erythematosus, characterized mainly by congenital heart block and transient skin lesions, is usually self-limited. A patient with history of neonatal lupus erythematosus and congenital heart block developed central nervous system vasculopathy resembling moyamoya disease and hypertension at 17 years of a...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(01)00344-7

    authors: Inoue K,Fukushige J,Ohno T,Igarashi H,Hara T

    更新日期:2002-01-01 00:00:00

  • Childhood Moyamoya: Looking Back to the Future.

    abstract::Moyamoya is a chronic, progressive steno-occlusive arteriopathy that typically affects the anterior circulation arteries of the circle of Willis. A network of deep thalamoperforating and lenticulostriate collaterals develop to by-pass the occlusion giving rise to the characteristic angiographic "puff of smoke" appeara...

    journal_title:Pediatric neurology

    pub_type: 杂志文章,评审

    doi:10.1016/j.pediatrneurol.2018.10.006

    authors: Dlamini N,Muthusami P,Amlie-Lefond C

    更新日期:2019-02-01 00:00:00