Werdnig-Hoffmann: Dominant Inheritance

J Gordon Millichap

doi:10.15844/pedneurbriefs-6-10-7

Werdnig-Hoffmann: Dominant Inheritance

Pediatric Neurology Briefs

Volume 6 (1992): Issue 10

By: J Gordon Millichap

Open Access

|Oct 1992

Abstract

A family in which both Werdnig-Hoffmann disease and chronic distal spinal muscular atrophy occurred, with apparent autosomal dominant inheritance, is reported from the Department of Neurology, Mayo Clinic Jacksonville, FL and Johns Hopkins University School of Medicine, Baltimore, MD.

References

Boylan KB Cornblath DR Werdnig-Hoffmann disease and chronic distal spinal muscular atrophy with apparent autosomal dominant inheritance Ann Neurol 1992 Sep 32 3 404 407 10.1002/ana.410320318 1416812
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Russman BS Ann Neurol 1992 Sept 32 439 (abstr)
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Miles DK Ann Neurol 1992 Sept 32 466 (abstr)
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-6-10-7 | Journal eISSN: 2166-6482

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Language: English

Page range: 78 - 79

Published on: Oct 1, 1992

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Werdnig-Hoffmann Disease,

Autosomal Dominant Inheritance,

Neonatal Adrenoleukodystrophy

© 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 10