Juvenile Leigh's Encephalomyelopathy With Peripheral Neuropathy, Myopathy, and Cardiomyopathy

Author:

Grunnet Margaret L.1,Zalneraitis Edwin L.2,Russman Barry S.3,Barwick Morven C.4

Affiliation:

1. Department of Neurology, University of Connecticut Health Center, Farmington, Department of Pathology, University of Connecticut Health Center, Farmington

2. Department of Neurology, University of Connecticut Health Center, Farmington, Department of Pediatrics, University of Connecticut Health Center, Farmington

3. Department of Pediatric Neurology, Newington Children's Hospital, Newington, CT

4. Department of Neurology, University of Connecticut Health Center, Farmington

Abstract

A child with typical histopathologic changes of Leigh's subacute necrotizing encephalomyelopathy presented with a chronic demyelinating neuropathy. During her 11-year course, she developed an unusual myopathy and cardiomyopathy in addition to many of the previously described manifestations of Leigh's disease. Despite an extensive evaluation, the biochemical basis of her condition was never identified. This case demonstrates another unique constellation of clinical alterations associated with subacute necrotizing encephalomyelopathy, and that chronic demyelinating neuropathy can be an important initial presentation of the disease. (J Child Neurol 1991;6:159-163).

Publisher

SAGE Publications

Subject

Neurology (clinical),Pediatrics, Perinatology and Child Health

Cited by 11 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. L;Taybi and Lachman's Radiology of Syndromes, Metabolic Disorders and Skeletal Dysplasias;2007

2. Acute Flaccid Paralysis as Initial Symptom in 4 Patients with Novel E1α Mutations of the Pyruvate Dehydrogenase Complex;Neuropediatrics;2006-09-11

3. Atypical Presentations of Leigh Syndrome: A Case Series and Review;Pediatric Neurology;2005-05

4. Juvenile-Onset Leigh Syndrome With an Acute Polyneuropathy at Presentation;Journal of Child Neurology;2003-08

5. Mitochondrial encephalopathies;Seminars in Pediatric Neurology;1996-12

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