Differential diagnosis of perinatal hypophosphatasia: radiologic perspectives

Perinatal hypophosphatasia (HPP) is a rare, potentially life-threatening, inherited, systemic metabolic bone disease that can be difficult to recognize in utero and postnatally. Diagnosis is challenging because of the large number of skeletal dysplasias with overlapping clinical features. This revie...

Descripción completa

Detalles Bibliográficos
Autores principales: Offiah, Amaka C., Vockley, Jerry, Munns, Craig F., Murotsuki, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2018
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6313373/
https://www.ncbi.nlm.nih.gov/pubmed/30284005
http://dx.doi.org/10.1007/s00247-018-4239-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6313373/
https://www.ncbi.nlm.nih.gov/pubmed/30284005
http://dx.doi.org/10.1007/s00247-018-4239-0

Ejemplares similares