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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Bibliografiske detaljer
Udgivet i:Front Pediatr
Main Authors: di Palmo, Emanuela, Gallucci, Marcella, Tronconi, Elena, Bergamaschi, Rosalba, Cazzato, Salvatore, La Scola, Claudio, Ricci, Giampaolo, Pession, Andrea
Format: Artigo
Sprog:Inglês
Udgivet: Frontiers Media S.A. 2018
Fag:
Pediatrics
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6079206/
https://ncbi.nlm.nih.gov/pubmed/30109220
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fped.2018.00213
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