Literature DB >> 12874403

Autosomal dominant acute necrotizing encephalopathy.

D E Neilson1, R M Eiben, S Waniewski, C L Hoppel, M E Varnes, B A Bangert, M Wiznitzer, M L Warman, D S Kerr.   

Abstract

OBJECTIVE: To define the clinical and biochemical abnormalities of an autosomal dominant form of acute encephalopathy.
METHODS: The clinical details of 11 affected family members in comparison with 63 unaffected relatives were analyzed.
RESULTS: Affected children become comatose after onset of a febrile illness. Outcomes include full recovery, permanent neurologic impairment, and death. Recurrences produce more severe impairments. Lesions of necrotizing encephalopathy of the thalamus and brainstem are present on autopsy and MRI. Oxidative phosphorylation of intact mitochondria from a muscle biopsy shows loose coupling. Unaffected family members, including obligate carriers, share no clinical characteristics, demonstrating incomplete penetrance.
CONCLUSIONS: Characteristic pathology and MRI findings define this disorder of autosomal dominant acute encephalopathy. Leigh syndrome and sporadic acute necrotizing encephalopathy share similarities but are distinct.

Entities:  

Mesh:

Year:  2003        PMID: 12874403     DOI: 10.1212/01.wnl.0000073544.28775.1a

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  21 in total

Review 1.  Untreated recurrent acute necrotising encephalopathy associated with RANBP2 mutation, and normal outcome in a Caucasian boy.

Authors:  Ne-Ron Loh; Donald Barry Appleton
Journal:  Eur J Pediatr       Date:  2010-05-15       Impact factor: 3.183

2.  Acute necrotizing encephalopathy: combined therapy and favorable outcome in a new case.

Authors:  Renzo Manara; Malida Franzoi; Paola Cogo; Pier Antonio Battistella
Journal:  Childs Nerv Syst       Date:  2006-03-14       Impact factor: 1.475

3.  Acute necrotizing encephalopathy in 3 brothers.

Authors:  Elysa J Marco; Jane E Anderson; Derek E Neilson; Jonathan B Strober
Journal:  Pediatrics       Date:  2010-02-08       Impact factor: 7.124

4.  Impairments in age-dependent ubiquitin proteostasis and structural integrity of selective neurons by uncoupling Ran GTPase from the Ran-binding domain 3 of Ranbp2 and identification of novel mitochondrial isoforms of ubiquitin-conjugating enzyme E2I (ubc9) and Ranbp2.

Authors:  Hemangi Patil; Dosuk Yoon; Reshma Bhowmick; Yunfei Cai; Kyoung-In Cho; Paulo A Ferreira
Journal:  Small GTPases       Date:  2017-09-29

Review 5.  Decreased T2 signal in the thalami may be a sign of lysosomal storage disease.

Authors:  Taina Autti; Raimo Joensuu; Laura Aberg
Journal:  Neuroradiology       Date:  2007-03-03       Impact factor: 2.804

6.  Acute encephalopathy with bilateral thalamotegmental involvement and a benign course: a case report from Brazil.

Authors:  Regina Maria Papais Alvarenga; Vanderson Carvalho Neri; Tatiane Mendonça; Solange Camargo
Journal:  BMJ Case Rep       Date:  2011-06-30

7.  Acute necrotizing encephalopathy (ANE1): rare autosomal-dominant disorder presenting as acute transverse myelitis.

Authors:  Katharina Wolf; Thomas Schmitt-Mechelke; Spyridon Kollias; Armin Curt
Journal:  J Neurol       Date:  2013-01-18       Impact factor: 4.849

8.  Haploinsufficiency of RanBP2 is neuroprotective against light-elicited and age-dependent degeneration of photoreceptor neurons.

Authors:  K-in Cho; H Yi; A Yeh; N Tserentsoodol; L Cuadrado; K Searle; Y Hao; P A Ferreira
Journal:  Cell Death Differ       Date:  2008-10-24       Impact factor: 15.828

9.  Infection-triggered familial or recurrent cases of acute necrotizing encephalopathy caused by mutations in a component of the nuclear pore, RANBP2.

Authors:  Derek E Neilson; Mark D Adams; Caitlin M D Orr; Deborah K Schelling; Robert M Eiben; Douglas S Kerr; Jane Anderson; Alexander G Bassuk; Ann M Bye; Anne-Marie Childs; Antonia Clarke; Yanick J Crow; Maja Di Rocco; Christian Dohna-Schwake; Gregor Dueckers; Alfonso E Fasano; Artemis D Gika; Dimitris Gionnis; Mark P Gorman; Padraic J Grattan-Smith; Annette Hackenberg; Alice Kuster; Markus G Lentschig; Eduardo Lopez-Laso; Elysa J Marco; Sotiria Mastroyianni; Julie Perrier; Thomas Schmitt-Mechelke; Serenella Servidei; Angeliki Skardoutsou; Peter Uldall; Marjo S van der Knaap; Karrie C Goglin; David L Tefft; Cristin Aubin; Philip de Jager; David Hafler; Matthew L Warman
Journal:  Am J Hum Genet       Date:  2009-01       Impact factor: 11.025

10.  Ranbp2 haploinsufficiency mediates distinct cellular and biochemical phenotypes in brain and retinal dopaminergic and glia cells elicited by the Parkinsonian neurotoxin, 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP).

Authors:  Kyoung-In Cho; Kelly Searle; Mason Webb; Haiqing Yi; Paulo A Ferreira
Journal:  Cell Mol Life Sci       Date:  2012-07-21       Impact factor: 9.261

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.