Article
A case of dyskeratosis congenita with prominent splenomegaly, portal hypertension, and hypoxemia
2022-04-07
Abstract excerpt
<h4>Background: </h4> Dyskeratosis congenita is a rare hereditary disease. A correct diagnosis of this disease might be delayed due to its rarity. Therefore, a deep understanding of the characteristics of this condition is necessary to assist in early diagnosis. Case presentation A 16-year-old male was admitted to the hospital with the complaint of abdominal pain. The patient was examined to consider the diagnosis...
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Identifiers and source
- Literature Corpus work
- 65f154de-f96c-5ae8-a5c8-83cacd5758c0
- DOI
- 10.21203/rs.3.rs-1485606/v1