X - Linked Hypophosphatemic Rickets: A diagnostic and therapeutic challenge
X-linked hypophosphatemia is a genetic disorder caused by PHEX gene mutations, which affects the encoding of a metalloprotease whose function is to inhibit fibroblastic growth factor —23 (FGF-23), promoting phosphate renal loss. Following we describe the case of a teenager diagnosed with a PHEX gen...
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| Hlavní autoři: | , , |
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| Médium: | Artigo |
| Jazyk: | Espanhol |
| Vydáno: |
Universidad de Antioquia
2021-07-01
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| Edice: | Iatreia |
| Témata: | |
| On-line přístup: | https://revistas.udea.edu.co/index.php/iatreia/article/view/342234/20804152 |
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