Literature DB >> 921312

Hereditary coproporphyria and epilepsy.

A B Houston, M J Brodie, M R Moore, G G Thompson, J B Stephenson.   

Abstract

A 9-year-old boy with mental deterioration and epilepsy suffered an acute attack of hereditary coproporphyria associated with worsening of seizure control. Leucocyte coproporphyrinogen oxidase activity was undetectable in the patient during this attack, and was reduced in his mother, a latent case. The complex relationship between porphyria, epilepsy, and anticonvulsant drugs is discussed.

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Year:  1977        PMID： 921312      PMCID： PMC1544641          DOI： 10.1136/adc.52.8.646

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN： 0003-9888            Impact factor:   3.791


  22 in total

Review 1.  PEDIATRIC ASPECTS OF THE PORPHYRIAS.

Authors:  J J CHISOLM
Journal:  J Pediatr       Date:  1964-02       Impact factor: 4.406

2.  Hereditary coproporphyria.

Authors:  H BERGER; A GOLDBERG
Journal:  Br Med J       Date:  1955-07-09

3.  The occurrence and determination of delta-amino-levulinic acid and porphobilinogen in urine.

Authors:  D MAUZERALL; S GRANICK
Journal:  J Biol Chem       Date:  1956-03       Impact factor: 5.157

4.  Protein measurement with the Folin phenol reagent.

Authors:  O H LOWRY; N J ROSEBROUGH; A L FARR; R J RANDALL
Journal:  J Biol Chem       Date:  1951-11       Impact factor: 5.157

5.  Hereditary coproporphyria.

Authors:  A Goldberg; C Rimington; A C Lochhead
Journal:  Lancet       Date:  1967-03-25       Impact factor: 79.321

6.  Hepatic delta-aminolaevulinic acid synthetase in an attack of hereditary coproporphyria and during remission.

Authors:  N McIntyre; A J Pearson; D J Allan; S Craske; G M West; M R Moore; A D Beattie; J Paxton; A Goldberg
Journal:  Lancet       Date:  1971-03-20       Impact factor: 79.321

7.  Minor epileptic status.

Authors:  E M Brett
Journal:  J Neurol Sci       Date:  1966 Jan-Feb       Impact factor: 3.181

8.  Intermittent acute porphyria--demonstration of a genetic defect in porphobilinogen metabolism.

Authors:  U A Meyer; L J Strand; M Doss; A C Rees; H S Marver
Journal:  N Engl J Med       Date:  1972-06-15       Impact factor: 91.245

9.  Diminished erythroid ferrochelatase activity in protoporphyria.

Authors:  S S Bottomley; M Tanaka; M A Everett
Journal:  J Lab Clin Med       Date:  1975-07

10.  Childhood epileptic encephalopathy with slow spike-wave. A statistical study of 80 cases.

Authors:  J J Chevrie; J Aicardi
Journal:  Epilepsia       Date:  1972-04       Impact factor: 5.864
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  5 in total

1.  Aucte intermittent porphyria and epilepsy.

Authors:  R Biagini; R Tignani; A R Fifi; L Nappini
Journal:  Arch Dis Child       Date:  1979-08       Impact factor: 3.791

2.  Coexistence of hereditary coproporphyria and epilepsy: coproporphyrinogen oxidase deficiency in liver and kidney.

Authors:  M Doss; R von Tiepermann; K H Pflüger
Journal:  J Neurol       Date:  1981       Impact factor: 4.849

3.  Hereditary coproporphyria: unusual nervous system involvement in two cases.

Authors:  C Casali; M Lo Monaco; L D'Alessandro; D Griso; A Amantea; G C Topi; P Tonali
Journal:  J Neurol       Date:  1984       Impact factor: 4.849

Review 4.  Management of attacks of acute porphyria.

Authors:  A C Laiwah; K E McColl
Journal:  Drugs       Date:  1987-11       Impact factor: 9.546

5.  Pathogenesis and treatment of acute intermittent porphyria: discussion paper.

Authors:  A C Laiwah; A Goldberg; M R Moore
Journal:  J R Soc Med       Date:  1983-05       Impact factor: 18.000
  5 in total

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