Secondary coproporphyrinuria in a patient with the full clinical picture of a hereditary acute hepatic porphyria. A misleading clinical and biochemical course [11]

Journal of Neurology

Volumn 249, Issue 9, 2002, Pages 1325-1326

  Oberndorfer, Stefan ^a   Hitzenberger, Peter ^a   Gruber, Wolfgang ^a   Seidel, Johannes ^a   Urbanits, Sabine ^a   Doss, Manfred ^a   Grisold, Wolfgang ^a  

^a KAISER FRANZ JOSEF HOSPITAL   (Austria)

Author keywords

[No Author keywords available]

Indexed keywords

AMINOLEVULINIC ACID; COPROPORPHYRIN; PORPHYRIN;

ADULT; ANAMNESIS; CASE REPORT; CLINICAL FEATURE; COPROPORPHYRIA; DIFFERENTIAL DIAGNOSIS; DISEASE COURSE; ELECTROPHYSIOLOGY; FEMALE; GENETIC DISORDER; GESTATIONAL AGE; HEME SYNTHESIS; HEPATIC PORPHYRIA; HUMAN; LETTER; MENTAL DISEASE; METABOLIC DISORDER; NERVE CONDUCTION; NEUROLOGIC DISEASE; NEUROLOGIC EXAMINATION; NUCLEAR MAGNETIC RESONANCE IMAGING; PORPHYRIN METABOLISM; PREGNANCY; PRIORITY JOURNAL; SEIZURE; TREATMENT FAILURE; URINALYSIS; VOMITING; WEIGHT REDUCTION;

ADULT; COPROPORPHYRINS; FEMALE; HUMANS; PATIENTS; PORPHYRIA, ACUTE INTERMITTENT; PREGNANCY;

EID: 0036037793     PISSN: 03405354     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00415-002-0797-y     Document Type: Letter

References (9)

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7. Acute intermittent porphyria: Clinicopathologic correlation. Report of case and review of the literature
8. Acute porphyrias: Diagnosis and management
9. Acute porphyric neuropathy during pregnancy - Effect of haematin therapy