High Incidence of Cranial Synostosis and Chiari I Malformation in Children With X‐Linked Hypophosphatemic Rickets (XLHR)

X‐linked hypophosphatemic rickets (XLHR) represents the most common form of genetic hypophosphatemia and causes rickets and osteomalacia in children because of increased FGF23 secretion and renal phosphate wasting. Even though cranial vault and craniovertebral anomalies of potential neurosurgical in...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:J Bone Miner Res
Egile Nagusiak: Rothenbuhler, Anya, Fadel, Nathalie, Debza, Yahya, Bacchetta, Justine, Diallo, Mamadou Tidiane, Adamsbaum, Catherine, Linglart, Agnès, Di Rocco, Federico
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: John Wiley and Sons Inc. 2018
Gaiak:
Original Articles
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC7816089/
https://ncbi.nlm.nih.gov/pubmed/30352126
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jbmr.3614
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