Literature DB >> 4056969

Differentiation of transient hyperammonemia of the newborn and urea cycle enzyme defects by clinical presentation.

M L Hudak, M D Jones, S W Brusilow.   

Abstract

We reviewed clinical data in 33 patients with transient hyperammonemia of the newborn (THAN): six previously unreported cases and 27 from the literature. Thirteen neonates with urea cycle enzyme deficiencies (UCED) served for comparison. No differences were found in the incidence of perinatal complications, route of delivery, Apgar scores, sex, or incidence or time of onset of seizures. On the other hand, neonates with THAN had significantly lower birth weights (mean +/- SEM 2282 +/- 78 gm vs 3336 +/- 222 gm, P less than 0.001) and gestational ages (35.1 +/- 0.5 weeks vs 39.6 +/- 0.5 weeks, P less than 0.001). Mean time of onset of respiratory distress (3.9 +/- 1.4 hours vs 71.5 +/- 26.1 hours, P less than 0.001), ventilatory support (P less than 0.001), lethargy (P less than 0.005), and coma (P less than 0.005) occurred earlier in THAN. Distinctive laboratory findings in patients with THAN included abnormal chest radiographic findings and plasma ammonium concentrations that were higher (1871 +/- 209 microM vs 973 +/- 169 microM, P less than 0.02) at an earlier age. Respiratory distress occurred in all but one patient with THAN before 24 hours; in contrast, only 62% of infants with UCED had respiratory symptoms, and none before 30 hours. In this retrospective study, the clinical presentation alone differentiated THAN from UCED.

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Year:  1985        PMID: 4056969     DOI: 10.1016/s0022-3476(85)80398-x

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  14 in total

Review 1.  Detection of inborn errors of metabolism in the newborn.

Authors:  A Chakrapani; M A Cleary; J E Wraith
Journal:  Arch Dis Child Fetal Neonatal Ed       Date:  2001-05       Impact factor: 5.747

Review 2.  Transient hyperammonemia of newborn.

Authors:  L Krishnan; K K Diwakar; P Patil; N Bhaskaranand
Journal:  Indian J Pediatr       Date:  1996 Jan-Feb       Impact factor: 1.967

3.  Prospective versus clinical diagnosis and therapy of acute neonatal hyperammonaemia in two sisters with carbamyl phosphate synthetase deficiency.

Authors:  M Tuchman; S M Mauer; R A Holzknecht; M L Summar; C L Vnencak-Jones
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

Review 4.  Ornithine carbamoyl transferase deficiency: findings, models and problems.

Authors:  C Bachmann
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

5.  Argininosuccinase deficiency in a premature infant.

Authors:  W Wenner; A Hamosh
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

6.  Clinical Reasoning: An encephalopathic 3-day-old infant.

Authors:  A A Gelfand; A Sznewajs; H C Glass; A C Jelin; E H Sherr
Journal:  Neurology       Date:  2011-07-05       Impact factor: 9.910

7.  Alternative Start Sites Downstream of Non-Sense Mutations Drive Antigen Presentation and Tolerance Induction to C-Terminal Epitopes.

Authors:  Scott N Ashley; Suryanarayan Somanathan; Christian Hinderer; Maxwell Arias; Deirdre McMenamin; Christine Draper; James M Wilson
Journal:  J Immunol       Date:  2017-05-12       Impact factor: 5.422

8.  Hyperammonaemia with distal renal tubular acidosis.

Authors:  S G Miller; G J Schwartz
Journal:  Arch Dis Child       Date:  1997-11       Impact factor: 3.791

9.  Computerized tomography in primary hyperammonemia.

Authors:  J Olier; J Gallego; E Digon
Journal:  Neuroradiology       Date:  1989       Impact factor: 2.804

10.  Preimplantation genetic diagnosis for ornithine transcarbamylase deficiency by simultaneous analysis of duplex-nested PCR and fluorescence in situ hybridization: a case report.

Authors:  Hyoung-Song Lee; Jin Hyun Jun; Hye Won Choi; Chun Kyu Lim; Han-Wook Yoo; Mi Kyoung Koong; Inn Soo Kang
Journal:  J Korean Med Sci       Date:  2007-06       Impact factor: 2.153

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