Abstract
Variegate porphyria (VP) is an autosomal dominant disorder of porphyrin metabolism. We report a case of a 21-year-old male collegiate athlete who complained of recurrent headache and fatigue. Extensive testing after initial presentation failed to identify a cause. Months later, his grandmother was diagnosed with VP after being hospitalized; hence, he was tested. He was positive for a heterozygous missense mutation, R168H, in one protoporphyrinogen oxidase allele. This case highlights a rare disorder of heme synthesis that should be considered in the differential diagnosis of exertional fatigue and headaches in athletes. When other more common causes of fatigue and/or headache are unable to be identified, a more focused history and examination may lead to a more unusual but crucial diagnosis. To our knowledge, there are no reported cases of this condition in Division I collegiate athletes.
| Original language | English |
|---|---|
| Pages (from-to) | e58-e59 |
| Journal | Clinical Journal of Sport Medicine |
| Volume | 27 |
| Issue number | 4 |
| DOIs | |
| State | Published - Jul 1 2017 |
Keywords
- Fatigue
- Porphyria
- Protoporphyrinogen oxidase
- Variegate
- cutaneous
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