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A Case of GNE Myopathy Presenting a Rapid Deterioration during Pregnancy
Journal of Clinical Neurology ; : 280-282, 2013.
Article in English | WPRIM | ID: wpr-55539
ABSTRACT

BACKGROUND:

GNE myopathy is characterized by early-adult-onset distal myopathy sparing quadriceps caused by mutations in the GNE gene encoding UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase, an enzyme in the sialic-acid synthesis pathway. CASE REPORT A 27-year-old Korean woman presented a rapid deterioration in strength of the distal lower limbs during her first pregnancy. She was diagnosed with GNE myopathy and carrying the compound heterozygous mutations of the GNE gene (D208N/M29T).

CONCLUSIONS:

This is a representative case implying that an increased requirement of sialic acid during pregnancy might trigger a clinical worsening of GNE myopathy.
Subject(s)

Full text: Available Index: WPRIM (Western Pacific) Main subject: Phosphotransferases / Lifting / N-Acetylneuraminic Acid / Lower Extremity / Distal Myopathies / Muscular Diseases Limits: Adult / Female / Humans / Pregnancy Language: English Journal: Journal of Clinical Neurology Year: 2013 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Phosphotransferases / Lifting / N-Acetylneuraminic Acid / Lower Extremity / Distal Myopathies / Muscular Diseases Limits: Adult / Female / Humans / Pregnancy Language: English Journal: Journal of Clinical Neurology Year: 2013 Type: Article