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Myophosphorylase deficiency (McArdle disease) in a patient with normal pregnancy and normal pregnancy outcome
McArdle disease is a rare, mostly autosomal recessive disorder of deficient myophosphorylation of glycogen in skeletal muscles. Recent knowledge regarding this condition means that women of childbearing age with McArdle disease can expect to labour normally without ill effect. We report a case of a...
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| Vydáno v: | Obstet Med |
|---|---|
| Hlavní autoři: | , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
SAGE Publications
2011
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4989600/ https://ncbi.nlm.nih.gov/pubmed/27579106 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1258/om.2011.100015 |
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