Presentation and Diagnosis of Pediatric X-Linked Hypophosphatemia
X-linked hypophosphatemia (XLH) is a rare type of hereditary hypophosphatemic rickets. Patients with XLH have various symptoms that lower their QOL as defined by HAQ, RAPID3, SF36-PCS, and SF36-MCS in adult patients and SF-10 and PDCOI in pediatric patients. Early diagnosis and treatment are needed...
| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | English |
| Publicado em: |
MDPI AG
2023-02-01
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| Colecção: | Endocrines |
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| Acesso em linha: | https://www.mdpi.com/2673-396X/4/1/12 |