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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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| Foilsithe in: | Case Rep Pediatr |
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| Main Authors: | , , , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
Hindawi
2020
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| Ábhair: | |
| Rochtain Ar Líne: | 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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