Charcot-Marie-Tooth Hereditary Neuropathy Overview

Thomas D Bird

Charcot-Marie-Tooth Hereditary Neuropathy Overview

Review

In: GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993.

1998 Sep 28 [updated 2023 Feb 23].

Author

Thomas D Bird¹

Book Editors

Margaret P Adam, Jerry Feldman, Ghayda M Mirzaa, Roberta A Pagon, Stephanie E Wallace, Lora JH Bean, Karen W Gripp, Anne Amemiya

Affiliation

¹ Seattle VA Medical Center;, Departments of Neurology and Medicine, University of Washington, Seattle, Washington

PMID: 20301532
Bookshelf ID: NBK1358

Excerpt

The purpose of this overview is to increase the awareness of clinicians regarding Charcot-Marie-Tooth (CMT) hereditary neuropathy, its causes, and its management. The following are the goals of this overview.

Goal 1: Describe the clinical characteristics of CMT hereditary neuropathy.

Goal 2: Review the causes of CMT hereditary neuropathy.

Goal 3: Provide an evaluation strategy to identify the cause of CMT hereditary neuropathy in a proband (when possible).

Goal 4: Inform genetic counseling of family members of an individual with CMT hereditary neuropathy.

Goal 5: Review management of CMT hereditary neuropathy.

Sections

Publication types

Review