Cargando…
Brief Clinical Report: Hypophosphatasia—Diagnostic Considerations and Treatment Outcomes in an Infant
Hypophosphatasia (HPP) is a rare, inherited metabolic bone disorder characterized by low serum alkaline phosphatase activity and impaired bone mineralization. Clinical manifestations and severity of symptoms vary widely in HPP, ranging from in utero death to isolated dental manifestations in adults....
Autores principales: | Duffus, Sara, Thrasher, Bradly, Calikoglu, Ali S. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5901473/ https://www.ncbi.nlm.nih.gov/pubmed/29808151 http://dx.doi.org/10.1155/2018/5719761 |
Ejemplares similares
-
Characterization of tracheobronchomalacia in infants with hypophosphatasia
por: Padidela, Raja, et al.
Publicado: (2020) -
Perinatal Hypophosphatasia in a Premature Infant
por: Sankaran, Deepika, et al.
Publicado: (2020) -
Prosthetic rehabilitation of hypophosphatasia: a case report
por: Bağiş, Bora, et al.
Publicado: (2008) -
Young woman with hypophosphatasia: A case report
por: Siami, Haleh, et al.
Publicado: (2022) -
Hypophosphatasia
por: Mornet, Etienne
Publicado: (2007)