https://www.selleckchem.com/pr....oducts/s-gsk1349572.
Unsupplemented patients with baseline deficiency showed persistently worse glycemic control vs. those with baseline repletion. Variants in fibroblast growth factor receptor-1 ( ) may either cause isolated hypogonadotropic hypogonadism (IHH) or Kallmann syndrome (KS). Although the relationship of genes classically involved in IHH with combined pituitary hormone deficiency (CPHD) is well established, variants in have been presented as a rare cause of this phenotype recently. Herein, we report an adopted 16-year-old male presented wit
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