Literature DB >> 7837763

Menstrual cycle and gonadal steroid effects on symptomatic hyperammonaemia of urea-cycle-based and idiopathic aetiologies.

W W Grody1, R J Chang, N M Panagiotis, D Matz, S D Cederbaum.   

Abstract

We report two female patients, one with a known inborn error of ureagenesis and the other of unknown cause, in whom recurrent, transient episodes of severe hyperammonaemia increased in frequency and severity with sexual maturity and parturition. Both responded to ovarian steroids administered continuously to suppress ovulation and menstruation, and ultimately to simple hysterectomy. These studies suggest a new therapeutic approach to defective ureagenesis in female patients and a relationship between ammonia production or disposal and the menstrual cycle.

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Year:  1994        PMID: 7837763     DOI: 10.1007/bf00711592

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


  31 in total

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Journal:  Presse Med       Date:  1988-04-30       Impact factor: 1.228

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Journal:  J Pediatr       Date:  1985-11       Impact factor: 4.406

8.  Treatment of hyperammonemic coma caused by inborn errors of urea synthesis.

Authors:  M L Batshaw; S W Brusilow
Journal:  J Pediatr       Date:  1980-12       Impact factor: 4.406

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Journal:  Adv Exp Med Biol       Date:  1982       Impact factor: 2.622

10.  Hyperornithinemia, hyperammonemia, and homocitrullinuria. A new disorder of amino acid metabolism associated with myoclonic seizures and mental retardation.

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  10 in total

Review 1.  Arginase-1 deficiency.

Authors:  Yuan Yan Sin; Garrett Baron; Andreas Schulze; Colin D Funk
Journal:  J Mol Med (Berl)       Date:  2015-10-14       Impact factor: 4.599

2.  Successful pregnancy in severe methylmalonic acidaemia.

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Journal:  J Inherit Metab Dis       Date:  1999-10       Impact factor: 4.982

Review 3.  Recurrent encephalopathy: NAGS (N-acetylglutamate synthase) deficiency in adults.

Authors:  A Cartagena; A N Prasad; C A Rupar; M Strong; M Tuchman; N Ah Mew; C Prasad
Journal:  Can J Neurol Sci       Date:  2013-01       Impact factor: 2.104

4.  Hyperammonemia due to Adult-Onset N-Acetylglutamate Synthase Deficiency.

Authors:  Anne-Els van de Logt; Leo A J Kluijtmans; Marleen C D G Huigen; Mirian C H Janssen
Journal:  JIMD Rep       Date:  2016-05-05

Review 5.  Contrasting features of urea cycle disorders in human patients and knockout mouse models.

Authors:  Joshua L Deignan; Stephen D Cederbaum; Wayne W Grody
Journal:  Mol Genet Metab       Date:  2007-10-22       Impact factor: 4.797

6.  Sudden unexpected fatal encephalopathy in adults with OTC gene mutations-Clues for early diagnosis and timely treatment.

Authors:  Catia Cavicchi; Maria Donati; Rossella Parini; Miriam Rigoldi; Mauro Bernardi; Francesca Orfei; Nicolò Gentiloni Silveri; Aniello Colasante; Silvia Funghini; Serena Catarzi; Elisabetta Pasquini; Giancarlo la Marca; Sean Mooney; Renzo Guerrini; Amelia Morrone
Journal:  Orphanet J Rare Dis       Date:  2014-07-16       Impact factor: 4.123

Review 7.  Late-Onset N-Acetylglutamate Synthase Deficiency: Report of a Paradigmatic Adult Case Presenting with Headaches and Review of the Literature.

Authors:  Catia Cavicchi; Chiara Chilleri; Antonella Fioravanti; Lorenzo Ferri; Francesco Ripandelli; Cinzia Costa; Paolo Calabresi; Paolo Prontera; Francesca Pochiero; Elisabetta Pasquini; Silvia Funghini; Giancarlo la Marca; Maria Alice Donati; Amelia Morrone
Journal:  Int J Mol Sci       Date:  2018-01-24       Impact factor: 5.923

Review 8.  Presentation and management of N-acetylglutamate synthase deficiency: a review of the literature.

Authors:  Aileen Kenneson; Rani H Singh
Journal:  Orphanet J Rare Dis       Date:  2020-10-09       Impact factor: 4.123

Review 9.  Contraceptive use in women with inherited metabolic disorders: a retrospective study and literature review.

Authors:  Jessica I Gold; Nina B Gold; Diva D DeLeon; Rebecca Ganetzky
Journal:  Orphanet J Rare Dis       Date:  2022-02-08       Impact factor: 4.123

10.  N-acetylglutamate synthase deficiency: an insight into the genetics, epidemiology, pathophysiology, and treatment.

Authors:  Nicholas Ah Mew; Ljubica Caldovic
Journal:  Appl Clin Genet       Date:  2011-08-24
  10 in total

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