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.
| Published in: | Pediatric Neurology Briefs |
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| Main Author: | |
| Format: | Article |
| Language: | English |
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Pediatric Neurology Briefs Publishers
1994-05-01
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| Subjects: | |
| Online Access: | https://www.pediatricneurologybriefs.com/articles/2807 |
| Summary: | 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. |
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| ISSN: | 1043-3155 2166-6482 |