Literature DB >> 16818176

Neuroimaging of phakomatoses.

Doris D M Lin1, Peter B Barker.   

Abstract

The phakomatoses are congenital disorders manifesting with central nervous system and cutaneous abnormalities. The structures predominantly affected are those of ectodermal origin, including the skin, nervous system, and eyes. The 4 most common phakomatoses are neurofibromatosis (types 1 and 2), tuberous sclerosis, Sturge-Weber disease, and von Hippel-Lindau disease. Imaging of the brain and spine in these disorders plays an important role in diagnosis, as well as determining the extent of involvement and guiding surgical interventions. This article reviews the application of x-ray computed tomography and magnetic resonance imaging to these disorders, as well as that of newer, "functional" imaging techniques such as positron emission tomography, magnetic resonance perfusion imaging, and spectroscopy.

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Year:  2006        PMID: 16818176     DOI: 10.1016/j.spen.2006.01.011

Source DB:  PubMed          Journal:  Semin Pediatr Neurol        ISSN: 1071-9091            Impact factor:   1.636


  3 in total

1.  Unidentified bright objects in neurofibromatosis type 1.

Authors:  Anita Choudhary; Suvasini Sharma; Naveen Sankhyan; Sheffali Gulati; Atin Kumar
Journal:  Indian J Pediatr       Date:  2010-03       Impact factor: 1.967

Review 2.  Charcot-Marie-Tooth syndrome and neurofibromatosis type 1 with multiple neurofibromas of the entire spinal nerve roots.

Authors:  David O Onu; Andrew W Hunn; Jens Peters-Willke
Journal:  BMJ Case Rep       Date:  2013-07-13

Review 3.  [Imaging of tumor predisposition syndromes].

Authors:  K Glutig; A Pfeil; D M Renz
Journal:  Radiologe       Date:  2021-06-25       Impact factor: 0.635

  3 in total

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