Literature DB >> 3123788

Lethal hyperammonaemic coma due to ornithine transcarbamylase deficiency presenting as brain stem encephalitis in a previously asymptomatic ten-year-old boy.

T Coskun1, I Ozalp, S Mönch, J Kneer.   

Abstract

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Year:  1987        PMID： 3123788     DOI： 10.1007/bf01800076

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


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  2 in total

1.  Partial ornithine transcarbamylase deficiency associated with recurrent hyperammonemia, lethargy and depressed sensorium.

Authors:  J Oizumi; W G Ng; R Koch; K N Shaw; L Sweetman; A Velazquez; G N Donnell
Journal:  Clin Genet       Date:  1984-06       Impact factor: 4.438

2.  Risk of serious illness in heterozygotes for ornithine transcarbamylase deficiency.

Authors:  M L Batshaw; M Msall; A L Beaudet; J Trojak
Journal:  J Pediatr       Date:  1986-02       Impact factor: 4.406
  2 in total
  3 in total

1.  Valproate-induced lethal hyperammonaemic coma in a carrier of ornithine carbamoyltransferase deficiency.

Authors:  A Tokatli; T Coşkun; S Cataltepe; I Ozalp
Journal:  J Inherit Metab Dis       Date:  1991       Impact factor: 4.982

2.  Significant hepatic involvement in patients with ornithine transcarbamylase deficiency.

Authors:  Renata C Gallagher; Christina Lam; Derek Wong; Stephen Cederbaum; Ronald J Sokol
Journal:  J Pediatr       Date:  2014-01-30       Impact factor: 4.406

3.  Late onset ornithine carbamoyl transferase deficiency in males.

Authors:  E Drogari; J V Leonard
Journal:  Arch Dis Child       Date:  1988-11       Impact factor: 3.791
  3 in total

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