Acyl-CoA Dehydrogenase Deficiency and RS
A female infant with medium-chain acyl-CoA dehyrogenase (MCAD) deficiency who was diagnosed with Rett syndrome at 3.5 years is reported from Twenteborg Hospital, Almelo, and Wilhelmina Kinderziekenhuis, Utrecht, The Netherlands.
| 發表在: | Pediatric Neurology Briefs |
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| 主要作者: | |
| 格式: | Article |
| 語言: | 英语 |
| 出版: |
Pediatric Neurology Briefs Publishers
1994-05-01
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| 主題: | |
| 在線閱讀: | https://www.pediatricneurologybriefs.com/articles/2807 |