نتایج جستجو برای: multicystic dysplastic kidney
تعداد نتایج: 225892 فیلتر نتایج به سال:
A disparity remains between graft survival of renal allografts from deceased donors and from living donors. A better understanding of the molecular mechanisms that underlie this disparity may allow the development of targeted therapies to enhance graft survival. Here, we used microarrays to examine whole genome expression profiles using tissue from 53 human renal allograft protocol biopsies obt...
AIMS AND OBJECTIVES To investigate the expression of CD10 and osteopontin in dentigerous cyst and ameloblastoma and to correlate their expression with neoplastic potentiality of dentigerous cyst and local invasion and risk of local recurrence in ameloblastoma. METHODS CD10 and osteopontin expression was studied by means of immunohistochemistry in 9 cases of dentigerous cysts (DC) and 17 cases...
Abdominal wall defects are associated with other intra-abdominal anomalies. We report two neonates with omphalocele associated with intra-abdominal anomalies. One neonate had multicystic kidney. Other neonate had duplication cyst of ileum which was missed during initial closure in neonatal life.
Two cases of fetal abdominal masses were discovered in utero by real-time ultrasound. They were diagnosed as follicle ovarian cysts and multicystic kidney in the early days of life. Ultrasound should be used on all pregnant women in the second trimester, not only for assessment of fetal growth and placental position, but also for prenatal diagnosis of fetal malformation and fetal abdominal mass...
I. Background: The urological management of multicystic dysplastic kidneys (MCDK) in the paediatric patient is controversial. Historically, MCDK was rare, presenting with a palpable mass or symptoms, and was managed with open nephrectomy. Wilms’ Tumour was listed on the differential diagnosis. Introduction of antenatal ultrasound (US) transformed MCDK into a common condition which is generally ...
I have read with interest the case report “Bilateral multicystic renal dysplasia with Potter sequence. A case with penile agenesis” by Dursun et al.1 The authors stated that the case “provides most symptoms of bilateral multicystic hereditary renal adysplasia (HRA)”. Although most cases of renal adysplasia (agenesis/ dysplasia) are sporadic, some cases are inherited. Hereditary renal adysplasia...
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