1.Preliminary study of glyceryl phenylbutyrate therapy for Ornithine transcarbamylase deficiency and a literature review.
Duo ZHOU ; Xiaohong SHANG ; Yu QIAO ; Yi CHENG ; Zinan YU ; Xinwen HUANG
Chinese Journal of Medical Genetics 2023;40(9):1107-1112
OBJECTIVE:
To evaluate the efficacy and safety of glyceryl phenylbutyrate (GPB) therapy for patients with Ornithine transcarbamylase deficiency (OTCD).
METHODS:
Two children with OTCD were selected as the study subjects, and their clinical manifestations, blood ammonia, liver enzymes, growth and development information following the treatment with GPB were retrospectively analyzed. A literature review was also carried out by searching the PubMed database for studies on the GPB treatment for urea cycle disorders.
RESULTS:
With the GPB treatment, the blood ammonia and liver enzyme level in both patients have decreased to the normal range within 3 months. Motor development in child 2 has improved. No adverse reaction was noted, except for transient palmar greasy smell and loss of appetite in child 1. Analysis of the literature showed that patients had lower ammonia exposure, lower annual incidence of hyperammonemic crisis, more actual protein intake and fewer adverse events during GPB treatment.
CONCLUSION
GPB is safe and effective for the treatment of OTCD.
Child
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Humans
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Ornithine Carbamoyltransferase Deficiency Disease/drug therapy*
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Phenylbutyrates/therapeutic use*
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Ammonia
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Retrospective Studies
2.Hyperammonemia in a Patient with Late-Onset Ornithine Carbamoyltransferase Deficiency.
Dae Eun CHOI ; Kang Wook LEE ; Young Tai SHIN ; Ki Ryang NA
Journal of Korean Medical Science 2012;27(5):556-559
Ornithine carbamoyltransferase (OTC) deficiency is a urea cycle disorder that causes the accumulation of ammonia, which can lead to encephalopathy. Adults presenting with hyperammonemia who are subsequently diagnosed with urea cycle disorders are rare. Herein, we report a case of a late-onset OTC deficient patient who was successfully treated with arginine, benzoate and hemodialysis. A 59-yr-old man was admitted to our hospital with progressive lethargy and confusion. Although hyperammonemia was suspected as the cause of the patient's mental changes, there was no evidence of chronic liver disease. A plasma amino acid and urine organic acid analysis revealed OTC deficiency. Despite the administration of a lactulose enema, the patient's serum ammonia level increased and he remained confused, leading us to initiate acute hemodialysis. After treatment with arginine, sodium benzoate and hemodialysis, the patient's serum ammonia level stabilized and his mental status returned to normal.
Age of Onset
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Ammonia/blood
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Arginine/therapeutic use
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Citrulline/blood
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Humans
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Hyperammonemia/*etiology
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Male
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Middle Aged
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Ornithine/blood
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Ornithine Carbamoyltransferase Deficiency Disease/complications/*diagnosis/drug therapy
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Pedigree
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Renal Dialysis
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Sodium Benzoate/therapeutic use