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Hyperglycemia with hypogonadism and growth hormone deficiency in a 17-year-old male with H Syndrome: The first case report from Syria

2023-09-25

Abstract excerpt

<h4>Background: </h4> The nucleoside transport capabilities of the human equilibrative nucleoside transporter-3 (hENT3) are disrupted by mutations in SLC29A3 (10q22.2), which are genes for the nucleoside transporter and are the cause of the unusual autosomal recessive disease known as H syndrome. As a result, histiocytic cells invade a number of organs. Case presentation: A 17-year-old Syrian male was admitted to...

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Literature Corpus work: 3921d8ba-a2be-53cc-8cf8-69451c02687b
DOI: 10.21203/rs.3.rs-3362111/v1

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