Literature DB >> 22768672

Successful prospective management of neonatal citrullinemia.

Hayato Go1, Takashi Imamura, Koichi Hashimoto, Kei Ogasawara, Osamu Sakamoto, Noriyuki Takubo, Nobuo Momoi, Mitsuaki Hosoya.   

Abstract

Classical citrullinemia generally involves hyperammonemic coma in the first few days of life and leads to neurological sequelae in survivors. We report a case of an elder sister who fell into a hyperammonemic coma on the fifth day after birth. She was successfully treated with intravenous benzoate and hemodialysis, and was subsequently diagnosed with citrullinemia on the basis of biochemical analysis. Two years later, a younger sister was born without prenatal diagnosis. We monitored plasma ammonia and citrulline levels after birth, and again diagnosed her with CTLN1 on the basis of biochemical and DNA analyses. There have been few reports of the prospective treatment of citrullinemia; however, our experience indicates the need for the prospective management and the rapid reduction of ammonia levels to avoid neonatal hyperammonemic coma and subsequent sequelae.

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Year:  2012        PMID: 22768672     DOI: 10.1515/jpem-2011-0422

Source DB:  PubMed          Journal:  J Pediatr Endocrinol Metab        ISSN: 0334-018X            Impact factor:   1.634


  1 in total

1.  The impact of ammonia levels and dialysis on outcome in 202 patients with neonatal onset urea cycle disorders.

Authors:  Nina Hediger; Markus A Landolt; Carmen Diez-Fernandez; Martina Huemer; Johannes Häberle
Journal:  J Inherit Metab Dis       Date:  2018-03-08       Impact factor: 4.982

  1 in total

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