The syndrome of inv dup (15): clinical, electroencephalographic, and imaging findings.

Abstract:

:The clinical and laboratory data of four pediatric patients and one adult patient with inverted duplication (inv dup) (15) are reported. The most evident findings were dysmorphic features with frontal bossing; genital abnormalities, such as macropenis or hypospadias; mental retardation; autistic behavior; and seizures. Two additional adults with inv dup (15) from other institutions were also diagnosed in our laboratory. Seizures and mental retardation were the reasons for their referral. The clinical picture of inv dup (15) seems to be quite variable since the phenotype can also be normal. However, karyotyping and fluorescent in-situ hybridization, focused in particular on chromosome 15, appear to be indicated in patients with dysmorphic phenotypes, such as the one present in our patients, and in subjects with early-onset seizures and psychomotor retardation with autistic features.

journal_name

J Child Neurol

authors

Buoni S,Sorrentino L,Farnetani MA,Pucci L,Fois A

doi

10.1177/088307380001500605

subject

Has Abstract

pub_date

2000-06-01 00:00:00

pages

380-5

issue

6

eissn

0883-0738

issn

1708-8283

journal_volume

15

pub_type

杂志文章
  • Neuropathological homology in true Galloway-Mowat syndrome.

    abstract::Galloway-Mowat syndrome is a rare condition that is likely hereditary though the underlying offending gene has not been identified, and is characterized by microcephaly and severe nephrotic syndrome culminating in childhood death. Some of the reported cases have abnormalities in neuronal migration and intractable seiz...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073810383982

    authors: Keith J,Fabian VA,Walsh P,Sinniah R,Robitaille Y

    更新日期:2011-04-01 00:00:00

  • Acute pseudotumoral hemicerebellitis in a child: a rare and distinct entity?

    abstract::A pseudotumoral presentation of acute hemicerebellitis is rare in pediatric age. The authors report a new single case study of a 7-year-old child with pseudotumoral unilateral cerebellitis mimicking an intracranial tumor, which clinically presented itself with signs of intracranial hypertension and mild contralateral ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073814545114

    authors: Alberini E,Vellante V,Zennaro F,Calligaris L,Barbi E,Carrozzi M,Devescovi R

    更新日期:2015-03-01 00:00:00

  • Ante- and perinatal factors for cerebral palsy: case-control study in Estonia.

    abstract::Establishing consistency between cerebral palsy registries in reporting of new cases enables more effective collaboration in terms of researching predisposing factors. To identify antenatal and intrapartum risk factors for cerebral palsy in the Estonian population, we undertook a matched case-control study of 153 chil...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/08830738050200080401

    authors: Stelmach T,Pisarev H,Talvik T

    更新日期:2005-08-01 00:00:00

  • Video and CD-ROM as a training tool for performing neurologic examinations of 1-year-old children in a multicenter epidemiologic study.

    abstract::In lieu of traditional training of examiners to identify cerebral palsy on a neurologic examination at age 1 year, we proposed an alternative approach using a multimedia training video and CD-ROM we developed after a two-step validation process. We hypothesized that use of CD-ROM interactive training will lead to reli...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,多中心研究

    doi:10.1177/08830738050200101001

    authors: Kuban KC,O'Shea M,Allred E,Leviton A,Gilmore H,DuPlessis A,Krishnamoorthy K,Hahn C,Soul J,O'Connor SE,Miller K,Church PT,Keller C,Bream R,Adair R,Miller A,Romano E,Bassan H,Kerkering K,Engelke S,Marshall D,Milow

    更新日期:2005-10-01 00:00:00

  • Study of nerve conduction and late responses in normal Chinese infants, children, and adults.

    abstract::Healthy Chinese individuals (n = 168), aged from 24 hours to 30 years, were studied to establish the following normal values: (1) motor conduction velocity, distal latency, amplitude, and F-wave velocity in the median, ulnar, tibial, and peroneal nerves; (2) H-reflex velocity and latency in the tibial nerve for all su...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389701200102

    authors: Cai F,Zhang J

    更新日期:1997-01-01 00:00:00

  • Practical aspects of conducting large-scale functional magnetic resonance imaging studies in children.

    abstract::The potential benefits of functional magnetic resonance imaging (MRI) for the investigation of normal development have been limited by difficulties in its use with children. We describe the practical aspects, including failure rates, involved in conducting large-scale functional MRI studies with normal children. Two h...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/08830738020170122201

    authors: Byars AW,Holland SK,Strawsburg RH,Bommer W,Dunn RS,Schmithorst VJ,Plante E

    更新日期:2002-12-01 00:00:00

  • Aiming at neuroblastoma and hitting other worthy targets.

    abstract::Neuroblastoma is, at once, the most common and deadly extracranial solid tumor of childhood. Efforts aimed at targeting the neural characteristics of these tumors have taught us much about neural crest cell biology, apoptosis induction in the nervous system, and neurotrophin receptor signaling and intracellular proces...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/0883073813483173

    authors: Schor NF

    更新日期:2013-06-01 00:00:00

  • Torticollis.

    abstract::Torticollis refers to a twisting of the head and neck caused by a shortened sternocleidomastoid muscle, tipping the head toward the shortened muscle, while rotating the chin in the opposite direction. Torticollis is seen at all ages, from newborns to adults. It can be congenital or postnatally acquired. In this review...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/0883073812469294

    authors: Tomczak KK,Rosman NP

    更新日期:2013-03-01 00:00:00

  • Psychologic and neurologic function following treatment for childhood temporal lobe astrocytoma.

    abstract::Seven school-aged children treated for temporal lobe astrocytomas with surgical resection and irradiation were prospectively tested to evaluate their intellectual, academic, personality, and neurologic status after therapy. At their most recent follow-up examination, neuropsychologic functioning was adequate in only t...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307388800300111

    authors: Mulhern RK,Kovnar EH,Kun LE,Crisco JJ,Williams JM

    更新日期:1988-01-01 00:00:00

  • Spectral Doppler imaging of vessels in the optic nerve of children.

    abstract::Elevation and blur of the optic disc margin with hyperemia and flame hemorrhages are classic features of papilledema that may not be present with mild elevations of the cerebral spinal fluid pressure. In children, the disc can be dramatically elevated with indistinct margins in pseudopapilledema. Children with equivoc...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073807304192

    authors: Miller M,Sable C,Chang T

    更新日期:2007-07-01 00:00:00

  • Postinfectious myasthenia gravis: report of two children.

    abstract::We report two children with transient myasthenia gravis preceded by viral illnesses. The first is a 5-year-old boy who developed oculobulbar weakness 2 weeks following a varicella-zoster infection. The second is a 4-year-old boy who developed facial diplegia and dysarthria several weeks following a viral pharyngitis. ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/08830738050200051501

    authors: Felice KJ,DiMario FJ,Conway SR

    更新日期:2005-05-01 00:00:00

  • Birth-related upper brachial plexus injuries in infants: operative and nonoperative approaches.

    abstract::Advances in intraoperative neuroelectrodiagnostic testing and microneurosurgical techniques have made it possible to accurately explore the brachial plexus of neonates. Since 1987, we have followed 250 infants with birth-related brachial plexus injuries, and successful operations have been completed on more than 70 in...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389400900202

    authors: Laurent JP,Lee RT

    更新日期:1994-04-01 00:00:00

  • Acute Flaccid Myelitis: A Single Pediatric Center Experience From 2014 to 2019.

    abstract:BACKGROUND:Acute flaccid myelitis has emerged as the leading cause of acute flaccid paralysis in children. Acute flaccid myelitis leads to significant physical disability; hence, objective outcome measures to study disease severity and progression are desirable. In addition, nerve transfer to improve motor function in ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073820939392

    authors: Patel R,Gombolay GY,Peljovich AE,Conklin J,Blackwell LS,Howarth R,Wolf DS,Upadhyayula SR,Verma S

    更新日期:2020-11-01 00:00:00

  • Quantitative EEG in young diabetics.

    abstract::The aim of this study was to investigate the influence of metabolic control on quantitative electroencephalographic (EEG) abnormalities in young diabetic patients. We compared quantitative EEGs of 44 insulin-dependent diabetic patients with age-matched controls. Furthermore, differences in EEG variables of diabetic pa...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389501000419

    authors: Hauser E,Strohmayer C,Seidl R,Birnbacher R,Lischka A,Schober E

    更新日期:1995-07-01 00:00:00

  • Cerebral aneurysms in a child with acquired immune deficiency syndrome during rapid immune reconstitution.

    abstract::A 12-year-old boy with perinatally acquired human immunodeficiency virus infection an d Centers for Disease Control and Prevention class C3 disease presented with acute onset of confusion and a right-sided movement disorder 5 months after beginning a new antiretroviral regimen. His CD4 count had been below 50 cells/mi...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/088307380201700613

    authors: Bonkowsky JL,Christenson JC,Nixon GW,Pavia AT

    更新日期:2002-06-01 00:00:00

  • A Model Program for Translational Medicine in Epilepsy Genetics.

    abstract::Recent technological advances in gene sequencing have led to a rapid increase in gene discovery in epilepsy. However, the ability to assess pathogenicity of variants, provide functional analysis, and develop targeted therapies has not kept pace with rapid advances in sequencing technology. Thus, although clinical gene...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073816685654

    authors: Smith LA,Ullmann JF,Olson HE,Achkar CM,Truglio G,Kelly M,Rosen-Sheidley B,Poduri A

    更新日期:2017-03-01 00:00:00

  • Primary antiphospholipid syndrome presenting with a branch retinal artery occlusion in a 15-year-old boy.

    abstract::Acute vascular events are rare in the pediatric population, but there is an association with the presence of antiphospholipid antibodies. When there is no other underlying medical disorder, this is referred to as primary antiphospholipid syndrome. We present a case of a 15-year-old boy who developed an acute superior ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380201700517

    authors: Saxonhouse MA,Bhatti MT,Driebe WT Jr,Freeman BE,Maria BL,Carney PR

    更新日期:2002-05-01 00:00:00

  • Automated tandem mass spectrometry for mass newborn screening for disorders in fatty acid, organic acid, and amino acid metabolism.

    abstract::Development of acylcarnitine and amino acid profiling using tandem mass spectrometry, and its application for use with dried blood specimens collected on filter-paper cards, has introduced an innovative new technology for detecting inborn errors of fatty acid, organic acid, and amino acid metabolism. From November 1, ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073899014001021

    authors: Naylor EW,Chace DH

    更新日期:1999-11-01 00:00:00

  • Longitudinal electroencephalographic (EEG) findings in pediatric anti-N-methyl-D-aspartate (anti-NMDA) receptor encephalitis: the Padua experience.

    abstract::To contribute to characterize electroencephalographic (EEG) activity in pediatric anti-N-methyl-d-aspartate (anti-NMDA) receptor encephalitis, we reviewed electroclinical data of 5 children with anti-NMDA receptor encephalitis diagnosed in our department. We identified 4 longitudinal electroencephalographic phases: in...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073813515947

    authors: Nosadini M,Boniver C,Zuliani L,de Palma L,Cainelli E,Battistella PA,Toldo I,Suppiej A,Sartori S

    更新日期:2015-02-01 00:00:00

  • Practice parameters in child neurology: do pediatricians use them?

    abstract::We assessed pediatrician awareness of the parameter ''Evaluating the first non-febrile seizure in children'' and how the concepts of this parameter were incorporated into practice. Although most reported caring for children with seizures, 60% were not aware of the practice parameter. When given the clinical scenario o...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073809332766

    authors: Bale JF Jr,Caplin DA,Bruse JD,Folland D

    更新日期:2009-12-01 00:00:00

  • Acute pseudobulbar palsy due to bilateral focal cortical damage: the opercular syndrome of Foix-Chavany-Marie.

    abstract::Two children are described who suddenly developed an encephalitic illness with intractable bilateral facial seizures. The seizures subsided over several days, but the children were left with the signs of pseudobulbar palsy and are unable to speak or swallow effectively. Bilateral destructive lesions in the opercular r...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307388900400213

    authors: Grattan-Smith PJ,Hopkins IJ,Shield LK,Boldt DW

    更新日期:1989-04-01 00:00:00

  • Brain tumors presenting as a seizure disorder in infants.

    abstract::Seizures occur in 25% to 40% of children with supratentorial tumors and are the presenting complaint in 10% to 15%. However, when divided by age, only 2% of children with seizures as the presenting complaint of brain tumors were less than 1 year of age. Three children, ranging in age from 20 days to 7 months and seen ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307388700200308

    authors: Rutledge SL,Snead OC 3rd,Morawetz R,Chandra-Sekar B

    更新日期:1987-07-01 00:00:00

  • Congenital Visual Impairment and Progressive Microcephaly Due to Lysyl-Transfer Ribonucleic Acid (RNA) Synthetase (KARS) Mutations: The Expanding Phenotype of Aminoacyl-Transfer RNA Synthetase Mutations in Human Disease.

    abstract::Aminoacyl-transfer ribonucleic acid (RNA) synthetases (ARSs) are a group of enzymes required for the first step of protein translation. Each aminoacyl-transfer RNA synthetase links a specific amino acid to its corresponding transfer RNA component within the cytoplasm, mitochondria, or both. Mutations in ARSs have been...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073814553272

    authors: McMillan HJ,Humphreys P,Smith A,Schwartzentruber J,Chakraborty P,Bulman DE,Beaulieu CL,FORGE Canada Consortium.,Majewski J,Boycott KM,Geraghty MT

    更新日期:2015-07-01 00:00:00

  • Macrodactyly and fibrous hamartoma in a child with tuberous sclerosis complex.

    abstract::A 10-year-old boy with tuberous sclerosis complex and macrodactyly of the right index and middle fingers is described. He also had a fibrous hamartoma at the front of the right wrist. The association of fibrous hamartoma and macrodactyly has not been previously described in tuberous sclerosis complex. ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073810375616

    authors: Sharma S,Sankhyan N,Gulati S,Kumar A,Srinivas M,Shukla B,Mathur SR

    更新日期:2011-01-01 00:00:00

  • Comorbid Medical Conditions in Friedreich Ataxia: Association With Inflammatory Bowel Disease and Growth Hormone Deficiency.

    abstract::Friedreich ataxia is a progressive degenerative disease with neurologic and cardiac involvement. This study characterizes comorbid medical conditions in a large cohort of patients with Friedreich ataxia. Patient diagnoses were collected in a large natural history study of 641 subjects. Prevalence of diagnoses in the c...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,多中心研究

    doi:10.1177/0883073816643408

    authors: Shinnick JE,Schadt K,Strawser C,Wilcox N,Perlman SL,Wilmot GR,Gomez CM,Mathews KD,Yoon G,Zesiewicz T,Hoyle C,Subramony SH,Yiu EM,Delatycki MB,Brocht AF,Farmer JM,Lynch DR

    更新日期:2016-08-01 00:00:00

  • Familial-Environmental Risk Factors in South African Children With Attention-Deficit Hyperactivity Disorder (ADHD): A Case-Control Study.

    abstract::We investigated familial and environmental risk factors in a cohort of South African children diagnosed with attention-deficit hyperactivity disorder (ADHD). A prospective, hospital-based case control study was conducted comprising 50 children diagnosed with ADHD and 50 matched non-ADHD controls. The adjusted effect o...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073814560630

    authors: van Dyk L,Springer P,Kidd M,Steyn N,Solomons R,van Toorn R

    更新日期:2015-09-01 00:00:00

  • Patterns of cerebral arterial injury in children with neurological disabilities.

    abstract::We reviewed the data from 215 consecutively imaged children who were referred because of neurologic disease. We specifically looked for evidence of cerebral arterial infarction in the form of focal brain damage in an arterial vascular distribution. Twenty-eight showed an arterial infarction pattern. All the major cere...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307388700200413

    authors: Baumann RJ,Carr WA,Shuman RM

    更新日期:1987-10-01 00:00:00

  • Meningismus is a commonly overlooked finding in tension-type headache in children and adolescents.

    abstract::At present, both migraine and tension-type headaches in children are believed to be chronic primary headaches. Meningeal signs in both cases are ignored or not examined, and the neurologic status is considered normal. This is the first study that focuses on meningeal signs in children with chronic headaches. The study...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/08830738060210050601

    authors: Almazov I,Brand N

    更新日期:2006-05-01 00:00:00

  • Neurofibromatosis 1: clinical review and exceptions to the rules.

    abstract::Neurofibromatosis 1 is an autosomal dominant, multisystem disorder with myriad clinical manifestations. Between 1991 and 1998, 495 adults and children were diagnosed with neurofibromatosis 1 at a specialized neurogenetics clinic in Sydney, Australia. This review establishes the prevalence of the clinical manifestation...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380201700812

    authors: Young H,Hyman S,North K

    更新日期:2002-08-01 00:00:00

  • Neurobiology of Rett syndrome.

    abstract::Girls with Rett syndrome display signs of neuronal dysfunction including mental retardation, seizures, stereotyped movements, and abnormal breathing and autonomic control. Decelerating head growth during infancy might reflect a disorder in production or pruning of neuronal synapses or both. Recent immunocytochemical s...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/08830738030180100501

    authors: Johnston MV,Mullaney B,Blue ME

    更新日期:2003-10-01 00:00:00