Literature DB >> 1548491

Bilateral striatal necrosis, dystonia and optic atrophy in two siblings.

V Leuzzi1, E Bertini, A M De Negri, M Gallucci, B Garavaglia.   

Abstract

Two siblings developed a neurological disorder in the first decade characterised by generalised dystonia, hypokinesia, and subacute visual loss. CT and serial MRI examinations showed bilateral lesions of the striatum, mainly in the putamen. The classification of these patients is discussed in relation to infantile bilateral striatal necrosis (IBSN), Leigh's disease, and Leber's optic neuropathy. The literature shows a clinical and aetiopathogenetic overlap between these syndromes. In our cases parental consanguinity and the involvement of a single generation suggest a new clinical condition with autosomal recessive transmission.

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Year:  1992        PMID: 1548491      PMCID: PMC488925          DOI: 10.1136/jnnp.55.1.16

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN: 0022-3050            Impact factor:   10.154


  31 in total

1.  [FAMILIAL INFANTILE ENCEPHALOPATHY WITH SYMMETRIC BILATERAL NECROSIS OF THE CORPUS STRIATUM].

Authors:  E BARGETON-FARKAS; A M COCHARD; H E BRISSAUD; O ROBAIN; J C LEBALLE
Journal:  J Neurol Sci       Date:  1964 Sep-Oct       Impact factor: 3.181

2.  Studies on Leber's optic neuropathy III.

Authors:  A Palan; A Stehouwer; L N Went
Journal:  Doc Ophthalmol       Date:  1989-01       Impact factor: 2.379

3.  Infantile bilateral striatal necrosis. Clinicopathological classification.

Authors:  T Mito; T Tanaka; L E Becker; S Takashima; J Tanaka
Journal:  Arch Neurol       Date:  1986-07

4.  Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy.

Authors:  D C Wallace; G Singh; M T Lott; J A Hodge; T G Schurr; A M Lezza; L J Elsas; E K Nikoskelainen
Journal:  Science       Date:  1988-12-09       Impact factor: 47.728

5.  Familial holotopistic striatal necrosis.

Authors:  K Miyoshi; T Matsuoka; S Mizushima
Journal:  Acta Neuropathol       Date:  1969       Impact factor: 17.088

Review 6.  Leigh syndrome, a mitochondrial encephalo(myo)pathy. A review of the literature.

Authors:  P M van Erven; J P Cillessen; E M Eekhoff; F J Gabreëls; W H Doesburg; W A Lemmens; J L Slooff; W O Renier; W Ruitenbeek
Journal:  Clin Neurol Neurosurg       Date:  1987       Impact factor: 1.876

7.  Holes in the brain.

Authors:  J Aicardi; N Gordon; B Hagberg
Journal:  Dev Med Child Neurol       Date:  1985-04       Impact factor: 5.449

8.  Chronic Leigh Disease: a genetic and biochemical study.

Authors:  A Plaitakis; W O Whetsell; J R Cooper; M D Yahr
Journal:  Ann Neurol       Date:  1980-04       Impact factor: 10.422

9.  CT scan appearances in Leigh's disease (subacute necrotizing encephalomyelopathy).

Authors:  K Hall; D Gardner-Medwin
Journal:  Neuroradiology       Date:  1978       Impact factor: 2.804

10.  Magnetic resonance imaging in a case of autopsy-proved adult subacute necrotizing encephalomyelopathy (Leigh's disease).

Authors:  J T Kissel; S Kolkin; D Chakeres; C Boesel; K Weiss
Journal:  Arch Neurol       Date:  1987-05
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  3 in total

1.  Late onset familial dystonia: could mitochondrial deficits induce a diffuse lesioning process of the whole basal ganglia system?

Authors:  D Caparros-Lefebvre; A Destee; H Petit
Journal:  J Neurol Neurosurg Psychiatry       Date:  1997-08       Impact factor: 10.154

2.  Biotin-responsive basal ganglia disease maps to 2q36.3 and is due to mutations in SLC19A3.

Authors:  Wen-Qi Zeng; Eiman Al-Yamani; James S Acierno; Susan Slaugenhaupt; Tammy Gillis; Marcy E MacDonald; Pinar T Ozand; James F Gusella
Journal:  Am J Hum Genet       Date:  2005-05-03       Impact factor: 11.025

3.  Leber's "plus": neurological abnormalities in patients with Leber's hereditary optic neuropathy.

Authors:  E K Nikoskelainen; R J Marttila; K Huoponen; V Juvonen; T Lamminen; P Sonninen; M L Savontaus
Journal:  J Neurol Neurosurg Psychiatry       Date:  1995-08       Impact factor: 10.154

  3 in total

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