Carbonic Anhydrase II Deficiency: A Rare Case of Severe Obstructive Sleep Apnea

The term osteopetrosis describes a group of rare hereditary diseases of the skeleton, characterized by an increase in bone density, caused by a defect in the development or function of osteoclasts. It comprises a clinically and genetically heterogeneous conditions ranging from infantile onset life-t...

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Detalles Bibliográficos
Autores principales: di Palmo, Emanuela, Gallucci, Marcella, Tronconi, Elena, Bergamaschi, Rosalba, Cazzato, Salvatore, La Scola, Claudio, Ricci, Giampaolo, Pession, Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6079206/
https://www.ncbi.nlm.nih.gov/pubmed/30109220
http://dx.doi.org/10.3389/fped.2018.00213

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6079206/
https://www.ncbi.nlm.nih.gov/pubmed/30109220
http://dx.doi.org/10.3389/fped.2018.00213

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