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CASE REPORT
Cerebral venous thrombosis as the first presentation of classical homocystinuria in an adult patient
  1. Emily Woods1,
  2. Charlotte Dawson1,
  3. Latha Senthil2,
  4. Tarekegn Geberhiwot3,4
  1. 1QE Hospital Birmingham, Birmingham, UK
  2. 2Department of Radiology, University of Birmingham, Birmingham, West Midlands, UK
  3. 3Department of Endocrinology, University Hospital of Birmingham, Birmingham, UK
  4. 4University of Birmingham, Institute of Metabolism and Systems Research, Birmingham, West Midlands, UK
  1. Correspondence to Dr Tarekegn Geberhiwot, Tarekegn.hiwot{at}uhb.nhs.uk

Summary

A 30-year-old woman presented with severe headache, dysarthria and right hemiparesis. She was treated for suspected viral encephalopathy and recovered over the following weeks although the headaches persisted. Two months later she was treated in-hospital for pulmonary embolism. The following year she was readmitted for increased frequency of headaches and was given a diagnosis of migraine. A subsequent MRI head scan was suggestive of longstanding venous sinus infarcts and neuroradiology review concluded that encephalitis had been the incorrect initial diagnosis. Subsequent investigations for an underlying cause of the two episodes of venous thrombosis revealed a total homocysteine level of >350 μmol/L (<15 μmol/L). An underlying diagnosis of homocystinuria secondary to cystathionine β-synthase deficiency was made although this metabolic condition is normally recognised in childhood. Treatment with pyridoxine and betaine normalised her homocysteine levels and she has had no further thrombotic event since.

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Footnotes

  • Contributors EW and TG wrote the manuscript. All authors reviewed the draft and approved the final version. TG and CD cared for the patient.

  • Competing interests None declared.

  • Patient consent Obtained.

  • Provenance and peer review Not commissioned; externally peer reviewed.