Literature DB >> 2127080

Hemimegalencephaly and neurofibromatosis.

R Cusmai1, P Curatolo, S Mangano, R Cheminal, B Echenne.   

Abstract

Hemimegalencephaly, which previously has been associated with a poor clinical course characterized by intractable seizures and severe encephalopathy, was found without these conditions in two children with neurofibromatosis. These children showed relatively similar and favourable prognostic features: no presence of seizures before one month, seizures controlled or absent, no focal neurological signs and peculiar EEG findings. In our opinion the absence of heterotopias and hamartomas can be related with less severe outcome.

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Year:  1990        PMID: 2127080     DOI: 10.1055/s-2008-1071490

Source DB:  PubMed          Journal:  Neuropediatrics        ISSN: 0174-304X            Impact factor:   1.947


  4 in total

Review 1.  A developmental and genetic classification for midbrain-hindbrain malformations.

Authors:  A James Barkovich; Kathleen J Millen; William B Dobyns
Journal:  Brain       Date:  2009-12       Impact factor: 13.501

2.  Hemimegalencephaly, hemihypertrophy and vascular lesions.

Authors:  A Cristaldi; F Vigevano; G Antoniazzi; M di Capua; A Andreuzzi; G Morselli; F Iorio; G Fariello; G Trasimeni; G F Gualdi
Journal:  Eur J Pediatr       Date:  1995-02       Impact factor: 3.183

3.  Cranio-orbital-temporal neurofibromatosis: An uncommon subtype of neurofibromatosis type-1.

Authors:  Nibedita Acharya; Manjoo S Reddy; Caroline T Paulson; Deepti Prasanna
Journal:  Oman J Ophthalmol       Date:  2014-01

Review 4.  Diagnostic Approach to Macrocephaly in Children.

Authors:  Andrea Accogli; Ana Filipa Geraldo; Gianluca Piccolo; Antonella Riva; Marcello Scala; Ganna Balagura; Vincenzo Salpietro; Francesca Madia; Mohamad Maghnie; Federico Zara; Pasquale Striano; Domenico Tortora; Mariasavina Severino; Valeria Capra
Journal:  Front Pediatr       Date:  2022-01-14       Impact factor: 3.418

  4 in total

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