Literature DB >> 1130176

A new form of prolonged transient tyrosinemia presenting with severe metabolic acidosis.

D M Danks, P Tippett, J Rogers.   

Abstract

Yet another form of tyrosinemia is described, in a young baby who developed metabolic acidosis and ceased to grow when weaned from breast milk onto a higher protein formula. Severe tyrosyluria and mild tyrosinemia cleared on a low-protein diet which also corrected the acidosis. However, restoration of growth required a normal protein intake with very greatly reduced amounts of phenylalanine and tyrosine. The metabolic fault later resolved spontaneously at about 12 months of age. Mental development appears normal and liver disease was never apparent. The patient and her mother both excrete quite large quantities of an unidentified peptide.

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Year:  1975        PMID: 1130176     DOI: 10.1111/j.1651-2227.1975.tb03823.x

Source DB:  PubMed          Journal:  Acta Paediatr Scand        ISSN: 0001-656X


  3 in total

1.  Expanding the phenotype of hawkinsinuria: new insights from response to N-acetyl-L-cysteine.

Authors:  Natalia Gomez-Ospina; Anna I Scott; Gia J Oh; Donald Potter; Veena V Goel; Lauren Destino; Nancy Baugh; Gregory M Enns; Anna-Kaisa Niemi; Tina M Cowan
Journal:  J Inherit Metab Dis       Date:  2016-08-03       Impact factor: 4.982

Review 2.  Food intolerance in humans.

Authors:  R H Herman; L Hagler
Journal:  West J Med       Date:  1979-02

Review 3.  Hawkinsinuria clinical practice guidelines: a Mexican case report and literature review.

Authors:  Héctor Cruz-Camino; Diana Laura Vazquez-Cantu; Alexandra Vanessa Zea-Rey; Jaime López-Valdez; Jorge Jiménez-Lozano; René Gómez-Gutiérrez; Consuelo Cantú-Reyna
Journal:  J Int Med Res       Date:  2019-07-25       Impact factor: 1.671

  3 in total

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