Hypophosphatasia and cleidocranial dysplasia—a case report and review of the literature: the role of the neurosurgeon
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),General Medicine,Pediatrics, Perinatology and Child Health
Link
https://link.springer.com/content/pdf/10.1007/s00381-021-05261-1.pdf
Reference11 articles.
1. Linglart A, Biosse-Duplan M (2016) Hypophosphatasia. Curr Osteoporos Rep 14(3):95–105. https://doi.org/10.1007/s11914-016-0309-0
2. Whyte MP (2016) Hypophosphatasia-aetiology, nosology, pathogenesis, diagnosis and treatment. Nat Rev Endocrinol 12(4):233–246. https://doi.org/10.1038/nrendo.2016.14
3. Bangura A, Wright L, Shuler T (2020) Hypophosphatasia: current literature for pathophysiology, clinical manifestations, diagnosis, and treatment. Cureus 12(6). https://doi.org/10.7759/cureus.8594
4. Rubecz I, Méhes K, Kluiber L, Bozzay L, Weisenbach J, Fenyvesi J (1974) Hypophosphatasia: screening and family investigation. Clin Genet 6(3):155–159. https://doi.org/10.1111/j.1399-0004.1974.tb00645.x
5. Jirapinyo C, Deraje V, Huang G, Gue S, Anderson PJ, Moore MH (2020) Cleidocranial dysplasia: management of the multiple craniofacial and skeletal anomalies. J Craniofac Surg 31(4)908-911. https://doi.org/10.1097/SCS.0000000000006306
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