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Reversible sensory neuropathy in mitochondrial trifunctional protein deficiency

Reversible sensory neuropathy in mitochondrial trifunctional protein deficiency

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_479e07f645cc4cebae7099a13d2b6deb

Reversible sensory neuropathy in mitochondrial trifunctional protein deficiency

About this item

Full title

Reversible sensory neuropathy in mitochondrial trifunctional protein deficiency

Publisher

Hoboken, USA: John Wiley & Sons, Inc

Journal title

JIMD Reports, 2022-05, Vol.63 (3), p.207-210

Language

English

Formats

Publication information

Publisher

Hoboken, USA: John Wiley & Sons, Inc

More information

Scope and Contents

Contents

Axonal peripheral neuropathy is a common complication of mitochondrial trifunctional protein (MTP) deficiency and long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency that is usually considered progressive. Current treatment strategies are not able to fully prevent neuropathic symptoms in the majority of patients. We herein report three sisters wi...

Alternative Titles

Full title

Reversible sensory neuropathy in mitochondrial trifunctional protein deficiency

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_479e07f645cc4cebae7099a13d2b6deb

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_479e07f645cc4cebae7099a13d2b6deb

Other Identifiers

ISSN

2192-8312,2192-8304

E-ISSN

2192-8312

DOI

10.1002/jmd2.12279

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