Coronary arteriopathy in a patient with Noonan phenotype: Case report
Noonan syndrome (NS) is a pleomorphic genetic disorder. Up to 50-80% of individuals have associated congenital heart disease. The scope of cardiac disease in NS is quite variable depending on the gene mutation. The most common forms of cardiac defects include pulmonary stenosis, hypertrophic cardiom...
محفوظ في:
| المؤلفون الرئيسيون: | , , , , |
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| التنسيق: | Artigo |
| اللغة: | Inglês |
| منشور في: |
Wolters Kluwer Medknow Publications
2024-05-01
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| سلاسل: | Annals of Pediatric Cardiology |
| الموضوعات: | |
| الوصول للمادة أونلاين: | https://journals.lww.com/10.4103/apc.apc_145_23 |
| الوسوم: |
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