Literature DB >> 10342600

Alexander's disease: unique presentation.

M K Gingold1, J B Bodensteiner, S S Schochet, M Jaynes.   

Abstract

Subacute necrotizing encephalomyelopathy (Leigh syndrome) refers to a nebulous disease entity characterized by lactic acidosis, a wide variety a clinical manifestations, and a consistent conglomeration of pathologic findings. Several abnormalities in metabolism have been delineated in association with Leigh syndrome, but many cases have no identified metabolic abnormality. We report a case that clinically, metabolically, and neuroradiologically appeared to be Leigh syndrome. In addition, our patient exhibited other unusual clinical findings, including ocular motility abnormalities. Neuropathologically, however, the diagnosis of Alexander's disease was confirmed. A review of the literature failed to find other cases of Alexander's disease reported with the metabolic abnormalities and clinical manifestations with which our patient presented.

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Mesh:

Year:  1999        PMID: 10342600     DOI: 10.1177/088307389901400510

Source DB:  PubMed          Journal:  J Child Neurol        ISSN: 0883-0738            Impact factor:   1.987


  6 in total

1.  Alexander disease: diagnosis with MR imaging.

Authors:  M S van der Knaap; S Naidu; S N Breiter; S Blaser; H Stroink; S Springer; J C Begeer; R van Coster; P G Barth; N H Thomas; J Valk; J M Powers
Journal:  AJNR Am J Neuroradiol       Date:  2001-03       Impact factor: 3.825

2.  Elevated GFAP induces astrocyte dysfunction in caudal brain regions: A potential mechanism for hindbrain involved symptoms in type II Alexander disease.

Authors:  Heather R Minkel; Tooba Z Anwer; Kara M Arps; Michael Brenner; Michelle L Olsen
Journal:  Glia       Date:  2015-07-17       Impact factor: 7.452

3.  The functional alteration of mutant GFAP depends on the location of the domain: morphological and functional studies using astrocytoma-derived cells.

Authors:  Tomokatsu Yoshida; Yasuko Tomozawa; Takayo Arisato; Yuji Okamoto; Hirofumi Hirano; Masanori Nakagawa
Journal:  J Hum Genet       Date:  2007-02-22       Impact factor: 3.172

4.  A case of infantile Alexander disease accompanied by infantile spasms diagnosed by DNA analysis.

Authors:  Jung Mu Lee; Ae Suk Kim; Sun Ju Lee; Sung Min Cho; Dong Seok Lee; Sung Min Choi; Doo Kwun Kim; Chang Seok Ki; Jong Won Kim
Journal:  J Korean Med Sci       Date:  2006-10       Impact factor: 2.153

5.  Alexander disease: a leukodystrophy caused by a mutation in GFAP.

Authors:  Anne B Johnson
Journal:  Neurochem Res       Date:  2004-05       Impact factor: 3.996

Review 6.  Metabolic etiologies in West syndrome.

Authors:  Seda Salar; Solomon L Moshé; Aristea S Galanopoulou
Journal:  Epilepsia Open       Date:  2018-03-14
  6 in total

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