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In a woman, severe headaches after eating meat
    Differential Diagnosis[Top] [Nav]
ornithine transcarbamylase deficiency
    Discussion -- not available online[Top] [Nav]
    Update Comments[Top] [Nav]
  • editorial on Hauser and Arn [107]
    Footnotes in Print Edition[Top] [Nav]
    (1) Ornithine transcarbamylase deficiency: adult onset of severe symptoms.
  Gilchrist JM, Coleman RA.   Ann Intern Med 1987 Apr;106(4):556-8.  Pubmed+Abstract  Similars
    (2a) Ornithine transcarbamylase deficiency--a cause of bizarre behavior in a man.
  DiMagno EP, Lowe JE, et al.   N Engl J Med 1986 Sep 18;315(12):744-7.  Pubmed  Similars
    (2b) Mosaicism for an intragenic deletion in a boy with mild ornithine transcarbamylase deficiency.
  Maddalena A, Sosnoski DM, et al.   N Engl J Med 1988 Oct 13;319(15):999-1003.  Pubmed  Similars
    (3) Scientific American Medicine.
  Rubenstein E, Federman DD, et al. NY: Scientific American: May 1986 15:IX:4.
    (4) The Metabolic Basis of Inherited Disease. 5th ed.
  Stanbury JB, et al. New York: McGraw-Hill, 1983: 414.
    (M) McKusick 311250 = ornithine transcarbamylase deficiency.
    New References[Top] [Nav]
    101.Use of immunocytochemical analysis of a duodenal biopsy specimen to identify a carrier of ornithine transcarbamylase deficiency.
  Hamano Y, Kodama H, et al.   N Engl J Med 1988 Jun 9;318(23):1521-3.  Pubmed  Similars
    102.Natural history of symptomatic partial ornithine transcarbamylase deficiency.
  Rowe PC, Newman SL, et al.   N Engl J Med 1986 Feb 27;314(9):541-7.  Pubmed+Abstract  Similars
    103.Long-term treatment of girls with ornithine transcarbamylase deficiency.
  Maestri NE, Brusilow SW, et al.   N Engl J Med 1996 Sep 19;335(12):855-9.  Pubmed+Abstract  Similars
    104.Cerebral dysfunction in asymptomatic carriers of ornithine transcarbamylase deficiency.
  Batshaw ML, Roan Y, et al.   N Engl J Med 1980 Feb 28;302(9):482-5.  Pubmed+Abstract  Similars
    105.Allopurinol-induced orotidinuria. A test for mutations at the ornithine carbamoyltransferase locus in women [see comments] [published erratum appears in N Engl J Med 1997 May 1;336(18):1335].
  Hauser ER, Finkelstein JE, et al.   N Engl J Med 1990 Jun 7;322(23):1641-5.  Pubmed+Abstract  Similars
    106.Hyperammonemia in women with a mutation at the ornithine carbamoyltransferase locus. A cause of postpartum coma [see comments].
  Arn PH, Hauser ER, et al.   N Engl J Med 1990 Jun 7;322(23):1652-5.  Pubmed  Similars
    107.Precarious balance of nitrogen metabolism in women with a urea-cycle defect [editorial; comment].
  Horwich AL, Fenton WA.   N Engl J Med 1990 Jun 7;322(23):1668-70.  Pubmed  Similars
    108.Hemolytic anemias and erythrocyte enzymopathies.
  Valentine WN, Tanaka KR, et al.   Ann Intern Med 1985 Aug;103(2):245-57.  Pubmed+Abstract  Similars

Lyon phenomenon
    109.The William Allan memorial award address: X-chromosome inactivation and the location and expression of X-linked genes.
  Lyon MF.   Am J Hum Genet 1988 Jan;42(1):8-16.  Pubmed  Similars
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    ©1986-2000 John Sotos, MD. All rights reserved.  Last updated 16:35 PDT on July 4, 2000.[Top]

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