Literature DB >> 8805171

Megalencephalic leukodystrophy in an Asian Indian ethnic group.

B S Singhal1, R D Gursahani, V P Udani, A A Biniwale.   

Abstract

Over a 10-year period, we reviewed 30 patients with leukodystrophy, megalencephaly, and a relatively benign course. Most of these patients (26) belonged to a distinctive ethnic group called the Agrawals. Head circumference exceeded the 95th percentile in 28 patients; 22 patients had seizures; 22 had pyramidal signs (16 more pronounced and 6 mild); and 16 had cerebellar ataxia. The median age of onset of symptoms was 1.8 years. Interictal electroencephalogram (EEG) was abnormal in 21 of 23 patients. The inheritance is possibly autosomal recessive.

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Year:  1996        PMID: 8805171     DOI: 10.1016/0887-8994(96)00048-3

Source DB:  PubMed          Journal:  Pediatr Neurol        ISSN: 0887-8994            Impact factor:   3.372


  26 in total

1.  Megalencephalic leukoencephalopathy with subcortical cysts.

Authors:  Monica Juneja; Suvasini Sharma
Journal:  Indian J Pediatr       Date:  2005-02       Impact factor: 1.967

2.  Van der Knaap disease: a rare disease with atypical features.

Authors:  Ujjawal Roy; Bhushan Joshi; Goutam Ganguly
Journal:  BMJ Case Rep       Date:  2015-07-23

3.  Macrocephaly, epilepsy and intracranial cysts: an image to remember.

Authors:  Mounika Endrakanti; Vijay Gonda; Arushi Gahlot Saini; Manphool Singhal
Journal:  BMJ Case Rep       Date:  2018-06-23

4.  Megalencephalic leukoencephalopathy with subcortical cysts in an adult: quantitative proton MR spectroscopy and diffusion tensor MRI.

Authors:  K Brockmann; J Finsterbusch; B Terwey; J Frahm; F Hanefeld
Journal:  Neuroradiology       Date:  2003-02-14       Impact factor: 2.804

5.  Infantile-onset leukoencephalopathy with discrepant mild clinical course.

Authors:  S Gulati; M Kabra; S Gera; M Ghosh; P S Menon; V Kalra
Journal:  Indian J Pediatr       Date:  2000-10       Impact factor: 1.967

6.  Mutations of MLC1 (KIAA0027), encoding a putative membrane protein, cause megalencephalic leukoencephalopathy with subcortical cysts.

Authors:  P A Leegwater; B Q Yuan; J van der Steen; J Mulders; A A Könst; P K Boor; V Mejaski-Bosnjak; S M van der Maarel; R R Frants; C B Oudejans; R B Schutgens; J C Pronk; M S van der Knaap
Journal:  Am J Hum Genet       Date:  2001-03-06       Impact factor: 11.025

7.  Vacuoliting megalencephalic leukoencephalopathy with subcortical cysts, mapped to chromosome 22qtel.

Authors:  M Topçu; C Gartioux; F Ribierre; C Yalçinkaya; E Tokus; N Oztekin; J S Beckmann; M Ozguc; E Seboun
Journal:  Am J Hum Genet       Date:  2000-02       Impact factor: 11.025

Review 8.  Prevalence of ataxia in children: a systematic review.

Authors:  Kristin E Musselman; Cristina T Stoyanov; Rhul Marasigan; Mary E Jenkins; Jürgen Konczak; Susanne M Morton; Amy J Bastian
Journal:  Neurology       Date:  2013-11-27       Impact factor: 9.910

9.  Vacuolating megalencephalic leukoencephalopathy with mild clinical course validated by diffusion tensor imaging and MR spectroscopy.

Authors:  Yi-Fang Tu; Cheng-Yu Chen; Chao-Ching Huang; Chang-Shin Lee
Journal:  AJNR Am J Neuroradiol       Date:  2004 Jun-Jul       Impact factor: 3.825

10.  Molecular pathogenesis of megalencephalic leukoencephalopathy with subcortical cysts: mutations in MLC1 cause folding defects.

Authors:  Anna Duarri; Oscar Teijido; Tania López-Hernández; Gert C Scheper; Herve Barriere; Ilja Boor; Fernando Aguado; Antonio Zorzano; Manuel Palacín; Albert Martínez; Gergely L Lukacs; Marjo S van der Knaap; Virginia Nunes; Raúl Estévez
Journal:  Hum Mol Genet       Date:  2008-08-30       Impact factor: 6.150

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