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Hyperornithinemia, Hyperammonemia, and Homocitrullinuria Syndrome Causing Severe Neonatal Hyperammonemia

  • Katherine Taylor WildEmail author
  • Rebecca D. Ganetzky
  • Marc Yudkoff
  • Lynne Ierardi-Curto
Research Report
Part of the JIMD Reports book series (JIMD, volume 44)

Abstract

Hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome (OMIM 238970) is an autosomal recessive disorder that is caused by a deficiency of mitochondrial ornithine transporter 1, resulting in dysfunction of the urea cycle. HHH is the rarest of the urea cycle disorders, reported in fewer than 100 patients. It is characterized by extreme phenotypic variability, including diverse ages of onset and severity of phenotype. We report the first confirmed instance of HHH syndrome in a premature infant (31 2/7 weeks) with severe hyperammonemia (1,300 μmol/L).

This case highlights the importance of considering HHH in the differential diagnosis for neonatal hyperammonemia. Because HHH is not detected by newborn screening, and the characteristic biochemical triad may be subtle or even absent, it has the potential to be underdiagnosed; however, making the diagnosis has critical therapeutic implications as treatment is distinct from other urea cycle defects. For instance, lysine supplementation is a beneficial treatment unique to HHH. Therefore, we present here a review of previously reported cases in order to demonstrate the full spectrum of the disease and highlight potentially diagnostic features.

Keywords

HHH syndrome Hyperammonemia Inborn Inborn errors Metabolism Urea cycle disorders 

Abbreviations

ASA

Argininosuccinate

CPS I

Carbamoyl phosphate synthetase I

CSF

Cerebrospinal fluid

DOL

Day of life

HHH

Hyperornithinemia-hyperammonemia-homocitrullinuria

INR

International normalized ratio

LP

Lumbar puncture

OTC

Ornithine transcarbamylase

TPN

Total parenteral nutrition

Notes

Acknowledgments

The authors thank the family for their participation in this work.

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Copyright information

© Society for the Study of Inborn Errors of Metabolism (SSIEM) 2018

Authors and Affiliations

  • Katherine Taylor Wild
    • 1
    Email author
  • Rebecca D. Ganetzky
    • 1
  • Marc Yudkoff
    • 1
  • Lynne Ierardi-Curto
    • 1
  1. 1.Division of Human Genetics, Department of Pediatrics, The Children’s Hospital of Philadelphia, Perelman School of MedicineUniversity of PennsylvaniaPhiladelphiaUSA

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