Literature DB >> 15856153

[HERNS. A rare, hereditary, multisystemic disease with cerebral microangiopathy].

C Seifried1, M Sitzer, J Jen, G Auburger.   

Abstract

Hereditary endotheliopathy with retinopathy, nephropathy, and stroke (HERNS) is an autosomally dominant inherited, multisystemic disease presenting with leukoencephalopathy, progressive visual loss, and nephropathy. Furthermore, psychiatric symptoms and migraine may occur. Magnetic resonance imaging has identified contrast-enhancing cerebral lesions with surrounding vasogenic edema. Electron microscopy has shown alterations in the arterioles and capillaries consisting of multilayered basement membranes in brain, kidney, and skin biopsies. Linkage analysis has mapped the disease locus to chromosome 3p21. At the present time, no effective treatment is known. This article gives a summary of the clinical, morphological, genetical, and pathological characteristics of HERNS.

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Year:  2005        PMID: 15856153     DOI: 10.1007/s00115-005-1910-0

Source DB:  PubMed          Journal:  Nervenarzt        ISSN: 0028-2804            Impact factor:   1.214


  13 in total

1.  The ocular manifestations in Fabry's disease.

Authors:  N A Sher; R D Letson; R J Desnick
Journal:  Arch Ophthalmol       Date:  1979-04

2.  Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3.

Authors:  R A Ophoff; J DeYoung; S K Service; M Joosse; N A Caffo; L A Sandkuijl; G M Terwindt; J Haan; A M van den Maagdenberg; J Jen; R W Baloh; M L Barilla-LaBarca; N L Saccone; J P Atkinson; M D Ferrari; N B Freimer; R R Frants
Journal:  Am J Hum Genet       Date:  2001-06-28       Impact factor: 11.025

3.  Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy.

Authors:  Sohei Yanagawa; Nobuo Ito; Kunimasa Arima; Shu-ichi Ikeda
Journal:  Neurology       Date:  2002-03-12       Impact factor: 9.910

4.  Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia.

Authors:  A Joutel; C Corpechot; A Ducros; K Vahedi; H Chabriat; P Mouton; S Alamowitch; V Domenga; M Cécillion; E Marechal; J Maciazek; C Vayssiere; C Cruaud; E A Cabanis; M M Ruchoux; J Weissenbach; J F Bach; M G Bousser; E Tournier-Lasserve
Journal:  Nature       Date:  1996-10-24       Impact factor: 49.962

5.  Cerebroretinal vasculopathy. A new hereditary syndrome.

Authors:  M G Grand; J Kaine; K Fulling; J Atkinson; S B Dowton; M Farber; J Craver; K Rice
Journal:  Ophthalmology       Date:  1988-05       Impact factor: 12.079

6.  Hereditary endotheliopathy with retinopathy, nephropathy, and stroke (HERNS).

Authors:  J Jen; A H Cohen; Q Yue; J T Stout; H V Vinters; S Nelson; R W Baloh
Journal:  Neurology       Date:  1997-11       Impact factor: 9.910

7.  Cerebroretinal vasculopathy mimicking a brain tumor: a case of a rare hereditary syndrome.

Authors:  S Weil; G Reifenberger; C Dudel; T A Yousry; S Schriever; S Noachtar
Journal:  Neurology       Date:  1999-08-11       Impact factor: 9.910

8.  Cerebroretinal vasculopathy and leukoencephalopathy mimicking a brain tumor. Report of two early-onset cases with Fanconi's anemia-like phenotypes suggesting an autosomal-recessive inheritance pattern.

Authors:  I Niedermayer; W Reiche; N Graf; P Mestres; W Feiden
Journal:  Clin Neuropathol       Date:  2000 Nov-Dec       Impact factor: 1.368

9.  Treatment of radiation-induced nervous system injury with heparin and warfarin.

Authors:  M J Glantz; P C Burger; A H Friedman; R A Radtke; E W Massey; S C Schold
Journal:  Neurology       Date:  1994-11       Impact factor: 9.910

10.  Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, genetic homogeneity, and mapping of the locus within a 2-cM interval.

Authors:  A Ducros; T Nagy; S Alamowitch; A Nibbio; A Joutel; K Vahedi; H Chabriat; M T Iba-Zizen; J Julien; P Davous; J Y Goas; O Lyon-Caen; B Dubois; X Ducrocq; F Salsa; M Ragno; P Burkhard; C Bassetti; M Hutchinson; M Vérin; F Viader; F Chapon; M Levasseur; J L Mas; O Delrieu
Journal:  Am J Hum Genet       Date:  1996-01       Impact factor: 11.025

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  2 in total

1.  Hereditary endotheliopathy with retinopathy and encephalopathy: pathological and genetic studies of a family.

Authors:  Yu-Hua Fan; Jian Sun; Yun Yuan; Ling Chen; Zhong Pei; Shi-Hui Xing; Bing Liao; Jin-Sheng Zeng
Journal:  Int J Clin Exp Pathol       Date:  2015-08-01

2.  Hereditary systemic angiopathy (HSA) with cerebral calcifications, retinopathy, progressive nephropathy, and hepatopathy.

Authors:  D T Winkler; P Lyrer; A Probst; D Devys; T Haufschild; S Haller; N Willi; M J Mihatsch; A J Steck; M Tolnay
Journal:  J Neurol       Date:  2008-01-22       Impact factor: 6.682

  2 in total

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