Familial Spastic Paraparesis as a Mitochondrial Disorder

J Gordon Millichap

doi:10.15844/pedneurbriefs-6-2-6

Familial Spastic Paraparesis as a Mitochondrial Disorder

Pediatric Neurology Briefs

Volume 6 (1992): Issue 2

By: J Gordon Millichap

Open Access

|Feb 1992

Abstract

A girl presenting at 6 years with familial spastic paraparesis and having deficiencies of respiratory chain enzyme complex I, III and IV is reported from the Departments of Pediatrics and Neurology, Loyola University Medical Center, Maywood, IL.

References

Beltran RS Coker SB Familial spastic paraparesis: a case of a mitochondrial disorder Pediatr Neurosurg 1991 16 1 40 42 10.1159/000120502 1966825
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-6-2-6 | Journal eISSN: 2166-6482

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Language: English

Page range: 12 - 13

Published on: Feb 1, 1992

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Familial Spastic Paraparesis,

Mitochondrial Disorder,

Cranial Nerve Deficits

© 1992 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 6 (1992): Issue 2