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First Case Report of EX3del4765 Mutation in PAH Gene in Asian Population
Gene Deletion Phenylalanine Hydroxylase Phenylketonuria
2016/1/26
Introduction: Phenylketonuria (PKU) is an autosomal recessive inborn error of phenylalanine metabolism, which is caused by mutation in phenylalanine hydroxylase (PAH) gene. Most of the PAH mutations a...
Malignant Priapism Due to Renal Cancer: A Case Report of First Manifestation of Systemic Spread
Priapism Metastasis Renal Cancer
2015/10/16
Introduction: Malignant priapism due to cancers is a rare condition that only 30 cases of kidney cancers were reported.
Introduction:: Amiodarone is an effective drug for life-threatening arrhythmias like recurrent ventricular fibrillation and atrial fibrillation. Amiodarone creates rarely genitourinary side effects ar...
Foreign Bodies in Lower Urinary Tract:Case Report and Review of Literature
Foreign Bodies Lower Urinary Tract Symptoms Urinary Tract Infections
2015/10/8
Foreign bodies in lower urinary tract may present in a different number of ways. We report four cases of such unusual presentation. Physical examination and plain radiograph was sufficient enough to c...
Persistent Müllerian Duct Syndrome with Transverse Testicular Ectopia: A Case Report with Literature Review
Persistent müllerian duct syndrome inguinal hernia
2009/6/23
Persistent mllerian duct syndrome (PMDS) is an uncommon form of male pseudohermaphroditism
characterized by the persistence of well developed mllerian duct structures in an otherwise nor...