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A Case of Congenital Disorder of Glycosylation Ia Presented with Recurrent Pericardial Effusion
Background: Inherited deficiency of phosophomannomutase (PMM2) causes a human glycosylation disorder known as Congenital Disorder of Glycosylation Ia. Case Presentation: Herein, we describe a case of congenital disorder of glycosylation Ia, presented with recurrent pericardial effusion and unusual f...
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| Vydáno v: | Iran J Pediatr |
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| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Tehran University of Medical Sciences
2014
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4359423/ https://ncbi.nlm.nih.gov/pubmed/25793077 |
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