טוען...
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...
שמור ב:
| הוצא לאור ב: | Obstet Med |
|---|---|
| Main Authors: | , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
SAGE Publications
2011
|
| נושאים: | |
| גישה מקוונת: | 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 |
| תגים: |
הוספת תג
אין תגיות, היה/י הראשונ/ה לתייג את הרשומה!
|