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Unusual first presentation of a metabolic disorder
Claire Emma Strauss1, Gayle Hann2
1Paediatrics, North Middlesex University Hospital NHS Trust, London, UK.
Insights
This case study highlights an unusual presentation of tyrosinaemia type 1 in an infant, characterized by neurological crisis and opisthotonic posturing. Early diagnosis and intervention are crucial for metabolic disorders to prevent severe complications.
Area of Science:
- Pediatrics
- Metabolic Disorders
- Genetics
Background:
- Tyrosinaemia type 1 is a rare genetic metabolic disorder.
- It primarily affects the liver and kidneys.
- Neurological complications can occur but are not typically the initial presentation.
Abstract:
An 8-month-old boy presented to hospital with a fever, irritability and 'back arching'. On examination, he demonstrated profound opisthotonic posturing and had tonsillitis. He had a full septic screen and was treated with broad spectrum antibiotics. Blood tests showed a transaminitis, raised alpha fetoprotein and deranged clotting. The clotting abnormalities and raised alpha fetoprotein persisted post discharge and an abdominal ultrasound showed steatosis, splenomegaly and bilateral increased renal cortical reflectivity. A full metabolic screen revealed type 1 tyrosinaemia. The opisthotonic posturing, a major part of this child's presentation, has not been reported as a presenting feature of tyrosinaemia. It was part of a 'neurological crisis' caused by tyrosinaemia and exacerbated by the intercurrent infection. These are known to occur in tyrosinaemia but not commonly as the first presentation. This represents an unusual presentation of a metabolic condition which, without intervention, can lead to severe hepatic, renal and neurodevelopmental complications.
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