The Rare Togetherness of Bladder Leiomyoma and Neurofibromatosis
Neurofibromatosis Type 1 (Von Recklinghausen disease) is a common, autosomal dominant hereditary disorder characterized by involvement of multiple tissues derived from the neural crest. Urinary system involvement in neurofibromatosis is a rare condition. Leiomyoma of the bladder is a rare benign mes...
| الحاوية / القاعدة: | Case Reports in Urology |
|---|---|
| المؤلفون الرئيسيون: | , , , , |
| التنسيق: | مقال |
| اللغة: | الإنجليزية |
| منشور في: |
Wiley
2018-01-01
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| الوصول للمادة أونلاين: | http://dx.doi.org/10.1155/2018/2302918 |