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.
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| Auteur principal: | |
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| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Pediatric Neurology Briefs Publishers
1994-05-01
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| Collection: | Pediatric Neurology Briefs |
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| Accès en ligne: | https://www.pediatricneurologybriefs.com/articles/2807 |
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