Literature DB >> 7732783

Identification of the characteristic vascular changes in a sural nerve biopsy of a case with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).

J M Schröder1, B Sellhaus, J Jörg.   

Abstract

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy' (CADASIL) has recently been identified as a hereditary disorder with characteristic fine structural changes of small intracerebral arteries and arterioles. Electron microscopically there are characteristic perivascular deposits of granular electron-dense material resembling immunoglobulin deposits. The present case from a family with four affected members in three successive generations shows that similar vascular changes as described in the central nervous system are present in blood vessels of the sural nerve, although less pronounced and, therefore, affording electron microscopy for their unequivocal detection. Nevertheless it has been shown for the first time that the diagnosis of CADASIL can be verified by a sural nerve biopsy. Occasional focal accumulation of pinocytotic vesicles opposite the granular deposits suggests exocytosis as one of the possible pathomechanisms for their production.

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Year:  1995        PMID: 7732783     DOI: 10.1007/bf00296354

Source DB:  PubMed          Journal:  Acta Neuropathol        ISSN: 0001-6322            Impact factor:   17.088


  23 in total

1.  Sclerosing vasculopathy of the central nervous system in nonelderly demented patients.

Authors:  M L Estes; M I Chimowitz; I A Awad; J T McMahon; A J Furlan; N B Ratliff
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2.  Slowly progressive familial dementia with recurrent strokes and white matter hypodensities on CT scan.

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3.  Hereditary multi-infarct dementia. Morphological and clinical studies of a new disease.

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4.  Electron-dense lipidic capillary deposits in Rett syndrome.

Authors:  R Dieler; J M Schröder; K Reddemann
Journal:  Acta Neuropathol       Date:  1990       Impact factor: 17.088

Review 5.  [Juvenile arteriosclerotic leukoencephalopathy: anatomoclinical study of a case].

Authors:  E Berthier; E Broussolle; M Garcia-Jacquier; M Tommasi; G Chazot
Journal:  Rev Neurol (Paris)       Date:  1992       Impact factor: 2.607

Review 6.  Mitochondrial abnormalities in human sural nerves: fine structural evaluation of cases with mitochondrial myopathy, hereditary and non-hereditary neuropathies, and review of the literature.

Authors:  J M Schröder; C Sommer
Journal:  Acta Neuropathol       Date:  1991       Impact factor: 17.088

7.  Autosomal dominant arteriopathic leuko-encephalopathy and Alzheimer's disease.

Authors:  F Gray; F Robert; R Labrecque; F Chrétien; M Baudrimont; C Fallet-Bianco; J Mikol; H V Vinters
Journal:  Neuropathol Appl Neurobiol       Date:  1994-02       Impact factor: 8.090

8.  Autosomal dominant syndrome with strokelike episodes and leukoencephalopathy.

Authors:  E Tournier-Lasserve; M T Iba-Zizen; N Romero; M G Bousser
Journal:  Stroke       Date:  1991-10       Impact factor: 7.914

9.  Significance of degenerating endoneurial cells in peripheral neuropathy.

Authors:  H Grehl; J M Schröder
Journal:  Acta Neuropathol       Date:  1991       Impact factor: 17.088

10.  Small arterial granular degeneration in familial Binswanger's syndrome.

Authors:  M Gutiérrez-Molina; A Caminero Rodríguez; C Martínez García; J Arpa Gutiérrez; C Morales Bastos; G Amer
Journal:  Acta Neuropathol       Date:  1994       Impact factor: 17.088

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  12 in total

1.  A patient with cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) confirmed by sural nerve biopsy.

Authors:  J Lechner-Scott; S Engelter; A Steck; S Dellas; M Tolnay; A Probst
Journal:  J Neurol Neurosurg Psychiatry       Date:  1996-02       Impact factor: 10.154

Review 2.  Single gene disorders causing ischaemic stroke.

Authors:  Saif S M Razvi; Ian Bone
Journal:  J Neurol       Date:  2006-06       Impact factor: 4.849

Review 3.  Neuropathology of Charcot-Marie-Tooth and related disorders.

Authors:  J Michael Schröder
Journal:  Neuromolecular Med       Date:  2006       Impact factor: 3.843

4.  Peripheral neuropathy in CADASIL.

Authors:  Francesco Sicurelli; Maria Teresa Dotti; Nicola De Stefano; Alessandro Malandrini; Mauro Mondelli; Silvia Bianchi; Antonio Federico
Journal:  J Neurol       Date:  2005-04-15       Impact factor: 4.849

5.  Nerve conduction studies in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

Authors:  Sa-Yoon Kang; Jung-Hwan Oh; Ji-Hoon Kang; Jay Chol Choi; Jung Seok Lee
Journal:  J Neurol       Date:  2009-06-02       Impact factor: 4.849

6.  Systemic vascular smooth muscle cell impairment in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

Authors:  M M Ruchoux; D Guerouaou; B Vandenhaute; J P Pruvo; P Vermersch; D Leys
Journal:  Acta Neuropathol       Date:  1995       Impact factor: 17.088

7.  Transgenic mice expressing mutant Notch3 develop vascular alterations characteristic of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

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8.  Role of electron microscopy in the diagnosis of cadasil syndrome: a study of 32 patients.

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Journal:  PLoS One       Date:  2013-06-17       Impact factor: 3.240

Review 9.  Neuropsychiatric manifestations in CADASIL.

Authors:  Hugues Chabriat; Marie-Germaine Bousser
Journal:  Dialogues Clin Neurosci       Date:  2007       Impact factor: 5.986

10.  Differences in proliferation rate between CADASIL and control vascular smooth muscle cells are related to increased TGFβ expression.

Authors:  Mahmod Panahi; Naeimeh Yousefi Mesri; Eva-Britt Samuelsson; Kirsten G Coupland; Charlotte Forsell; Caroline Graff; Saara Tikka; Bengt Winblad; Matti Viitanen; Helena Karlström; Erik Sundström; Homira Behbahani
Journal:  J Cell Mol Med       Date:  2018-03-13       Impact factor: 5.310

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