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Screening Children with a Family History of Central Congenital Hypoventilation Syndrome
Congenital central hypoventilation syndrome (CCHS) is a rare genetic disorder of an autonomic nervous disorder that affects breathing. It is characterized by respiratory insufficiency secondary to insensitivity to hypoxemia and hypercarbia, particularly during sleep leading to persistent apnea. We r...
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| Publicado no: | Case Rep Pediatr |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Hindawi
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7136801/ https://ncbi.nlm.nih.gov/pubmed/32274237 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2020/2713606 |
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