Literature DB >> 9659085

A prospective 10 year follow up study of patients with neurofibromatosis type 1.

M H Cnossen1, A de Goede-Bolder, K M van den Broek, C M Waasdorp, A P Oranje, H Stroink, H J Simonsz, A M van den Ouweland, D J Halley, M F Niermeijer.   

Abstract

OBJECTIVE: To establish the prevalence and incidence of symptoms and complications in children with neurofibromatosis type 1 (NF1) and to assess possible risk factors for the development of complications.
DESIGN: A 10 year prospective multidisciplinary follow up study. PATIENTS: One hundred and fifty children diagnosed with NF1 according to criteria set by the National Institutes of Health.
RESULTS: In 62 of 150 children (41.3%) complications were present, including 42 (28.0%) children with one complication, 18 (12.0%) with two complications, and two (1.3%) with three complications (mean (SD) duration of follow up 4.9 (3.8) years). Ninety five of the 150 children presented without complications (follow up, 340.8 person-years). The incidence of complications was 2.4/100 person-years in this group. An association was found between behavioural problems and the presence of complications.
CONCLUSION: This is the largest single centre case series of NF1 affected children followed until 18 years of age. Children with NF1, including those initially presenting without complications, should have regular clinical examinations.

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Year:  1998        PMID: 9659085      PMCID: PMC1717584          DOI: 10.1136/adc.78.5.408

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN: 0003-9888            Impact factor:   3.791


  7 in total

1.  A genetic study of von Recklinghausen neurofibromatosis in south east Wales. I. Prevalence, fitness, mutation rate, and effect of parental transmission on severity.

Authors:  S M Huson; D A Compston; P Clark; P S Harper
Journal:  J Med Genet       Date:  1989-11       Impact factor: 6.318

Review 2.  Neurogenic bladder dysfunction in children: review of pathophysiology and current management.

Authors:  E T Fernandes; Y Reinberg; R Vernier; R Gonzalez
Journal:  J Pediatr       Date:  1994-01       Impact factor: 4.406

Review 3.  A genetic study of von Recklinghausen neurofibromatosis in south east Wales. II. Guidelines for genetic counselling.

Authors:  S M Huson; D A Compston; P S Harper
Journal:  J Med Genet       Date:  1989-11       Impact factor: 6.318

4.  Emergence of optic pathway gliomas in children with neurofibromatosis type 1 after normal neuroimaging results.

Authors:  R Listernick; J Charrow; M Greenwald
Journal:  J Pediatr       Date:  1992-10       Impact factor: 4.406

5.  Natural history of optic pathway tumors in children with neurofibromatosis type 1: a longitudinal study.

Authors:  R Listernick; J Charrow; M Greenwald; M Mets
Journal:  J Pediatr       Date:  1994-07       Impact factor: 4.406

6.  The diagnosis of neurofibromatosis-1 in the child under the age of 6 years.

Authors:  A C Obringer; A T Meadows; E H Zackai
Journal:  Am J Dis Child       Date:  1989-06

7.  Visual-evoked responses in children with optic gliomas, with and without neurofibromatosis.

Authors:  M E Cohen; P K Duffner
Journal:  Childs Brain       Date:  1983
  7 in total
  25 in total

1.  Neurofibromatosis: chronological history and current issues.

Authors:  João Roberto Antônio; Eny Maria Goloni-Bertollo; Lívia Arroyo Trídico
Journal:  An Bras Dermatol       Date:  2013 May-Jun       Impact factor: 1.896

Review 2.  Spinal deformity in neurofibromatosis type-1: diagnosis and treatment.

Authors:  Athanasios I Tsirikos; Asif Saifuddin; M Hilali Noordeen
Journal:  Eur Spine J       Date:  2005-02-15       Impact factor: 3.134

3.  Phase I trial of pegylated interferon-alpha-2b in young patients with plexiform neurofibromas.

Authors:  R I Jakacki; E Dombi; D M Potter; S Goldman; J C Allen; I F Pollack; B C Widemann
Journal:  Neurology       Date:  2011-01-18       Impact factor: 9.910

4.  Posterior Spinal Reconstruction with Pedicle Screws, Multiple Iliac Screws and Wisconsin Spinal Wires in a Patient with Neurofibromatosis Scoliosis: A Case Report.

Authors:  Woong-Beom Kim; Young-Seop Park; Jong-Hwa Park; Seung-Jae Hyun
Journal:  Korean J Spine       Date:  2015-09-30

Review 5.  Neoplasms associated with germline and somatic NF1 gene mutations.

Authors:  Sachin Patil; Ronald S Chamberlain
Journal:  Oncologist       Date:  2012-01-12

6.  Natural history and management of low-grade glioma in NF-1 children.

Authors:  Pablo Hernáiz Driever; Stephan von Hornstein; Torsten Pietsch; Rolf Kortmann; Monika Warmuth-Metz; Angela Emser; Astrid K Gnekow
Journal:  J Neurooncol       Date:  2010-03-30       Impact factor: 4.130

7.  Midline cutaneous lumbosacral lesions: not always a sign of occult spinal dysraphism.

Authors:  Juan F Martínez-Lage; Belen Ferri Niguez; Miguel A Pérez-Espejo; María J Almagro; Concepción Maeztu
Journal:  Childs Nerv Syst       Date:  2006-02-01       Impact factor: 1.475

8.  Parents' experiences of caring for a young person with neurofibromatosis type 1 (NF1): a qualitative study.

Authors:  Jenny Barke; Jane Coad; Diana Harcourt
Journal:  J Community Genet       Date:  2015-07-23

9.  TERT promoter mutations and BRAF mutations are rare in sporadic, and TERT promoter mutations are absent in NF1-related malignant peripheral nerve sheath tumors.

Authors:  Hendrikus J Dubbink; Hannah Bakels; Edward Post; Ellen C Zwarthoff; Robert M Verdijk
Journal:  J Neurooncol       Date:  2014-07-18       Impact factor: 4.130

10.  Neurofibromatosis type 1 and sporadic optic gliomas.

Authors:  S Singhal; J M Birch; B Kerr; L Lashford; D G R Evans
Journal:  Arch Dis Child       Date:  2002-07       Impact factor: 3.791

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