Articles by author - Julia Matzen

Spinal cord atrophy in triple A syndrome associated with a novel compound heterozygous mutation.

Kunte H, Trendelenburg G, Matzen J, Ventz M, Kornak U, Harms L.

Case Reports 2010; 31(3): 301-303 PubMed PMID: 20588230  Keywords:  Adrenal Insufficiency:complications, Adult, Atrophy:complications, Esophageal Achalasia:complications, Heterozygote, Humans, Lacrimal Apparatus Diseases:complications, Male, Mutation, Nerve Tissue Proteins:genetics, Nuclear Pore Complex Proteins:genetics,.    Citation

: A 38-year-old male patient was admitted with slowly progressive spastic gait disturbance. Imaging revealed general spinal cord atrophy. .....

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