Rett Syndrome: A Mitochondrial Dysfunction?

J Gordon Millichap

doi:10.15844/pedneurbriefs-7-6-11

Rett Syndrome: A Mitochondrial Dysfunction?

Pediatric Neurology Briefs

Volume 7 (1993): Issue 6

By: J Gordon Millichap

Open Access

|Jun 1993

Abstract

Ultrastructural and biochemical alterations of muscle mitochondria are reported in two girls, aged 4 years, with Rett syndrome examined at the Institute of Neurological Sciences, University of Siena, Italy.

References

Dotti MT Manneschi L Malandrini A De Stefano N Caznerale F Federico A Mitochondrial dysfunction in Rett syndrome. An ultrastructural and biochemical study Brain Dev 1993 Mar-Apr 15 2 103 6 8214327 10.1016/0387-7604(93)90045-A
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Nielsen JB Toft PB Reske-Nielsen E Jensen KE Christiansen P Thomsen C Cerebral magnetic resonance spectroscopy in Rett syndrome. Failure to detect mitochondrial disorder Brain Dev 1993 Mar-Apr 15 2 107 12 8214328 10.1016/0387-7604(93)90046-B
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-7-6-11 | Journal eISSN: 2166-6482

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Language: English

Page range: 48 - 48

Published on: Jun 1, 1993

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Biochemical Alterations,

Cytochrome C Oxidase,

Dumb-Bell-Shaped

© 1993 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 7 (1993): Issue 6