ロード中...
Medium-chain Acyl-CoA dehydrogenase deficiency presenting with neonatal pulmonary haemorrhage
BACKGROUND: Medium-chain Acyl-CoA dehydrogenase deficiency (MCADD) is the most common inherited disorder of fatty acid beta-oxidation. Signs and symptoms of MCADD typically appear during infancy or early childhood and include vomiting, lethargy, and hypoglycemia. Pulmonary haemorrhage has previously...
保存先:
| 出版年: | Matern Health Neonatol Perinatol |
|---|---|
| 主要な著者: | , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2015
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4823675/ https://ncbi.nlm.nih.gov/pubmed/27057325 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40748-015-0010-9 |
| タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|