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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Format: | Book |
Published: |
Pediatric Neurology Briefs Publishers,
1994-05-01T00:00:00Z.
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Online Access: | Connect to this object online. |
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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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Item Description: | 1043-3155 2166-6482 10.15844/pedneurbriefs-8-5-7 |