نتایج جستجو برای: congenital renal anomalies

تعداد نتایج: 391005  

Aghayi, Shahrzad,

There is no English abstract.

2009
Lesley L. Breech Marc R. Laufer

The diagnosis and management of girls and young women with Müllerian anomalies requires not only knowledge of embryologic development, but an awareness of the known associations of structural anomalies of the female reproductive tract with other congenital anomalies, including renal anomalies and anorectal malformations. Recognition of such associations appropriately guides the diagnostic evalu...

Journal: :Archives of disease in childhood 1988
T R Gunn J D Mora P Pease

A prospective study was carried out during 1986 to find out the incidence of fetal renal tract anomalies in 3228 pregnant mothers delivered in one hospital. Ultrasound examination of the fetus was performed as part of the routine antenatal assessment at 16-20 weeks' gestation, and later examinations were done if there were obstetric indications. Fetuses with any degree of dilatation of the rena...

Journal: :Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine 2001
D M Sherer O Abulafia

artner duct cysts, the most common benign cystic lesion of the vagina, represent embryologic remnants of the caudal end of the mesonephric (wolffian) duct.1 These cysts are usually small and asymptomatic and have been reported to occur in as many as 1% of all women.1,2 Because the ureteral bud also develops from the wolffian duct, it is not surprising that Gartner duct cysts have been associate...

Journal: :The West Indian medical journal 2009
V DaCosta L Christie S Wynter J Harriott J Frederick

We present a case of a patient with Uterus bicornis bicollis, imperforate hemivagina and ipsilateral renal agenesis. This group of congenital malformations is often asymptomatic until puberty, when it presents as cyclic dysmenorrhoea, leucorrhoea or a pelvic mass. Magnetic resonance imaging is becoming the preferred modality for delineation of uterine malformations. When congenital abnormalitie...

ژورنال: پرستاری کودکان 2020

Introduction: Congenital anomalies are common causes of medical interventions, long-term illness and death. The aim of this study was to determine the risk factors of congenital anomalies in disabled patients under 15 years old registered in Welfare Organization of Shahrekord. Methods: The present study was a case–control study. 350 disabled patients registered in the Welfare Organization of Sh...

Abdulaziz O. Alabdulkarim, Alhanouf Alothri, Sara AlFadil, Sari M. Rabah, Shabeer A. Wani, Waleed Alshehri,

Aplasia Cutis Conginita (ACC) is a condition characterized by congenital absence of skin, usually on the scalp. ACC can occur as an isolated condition or in the presence of other congenital anomalies. Here we describe a case of a 16 days old baby girl with an isolated ACC of the scalp. Her elder two siblings have been diagnosed with ACC with concomitant cardiac or limb anomalies. The patient wa...

ژورنال: پوست و زیبایی 2019
Ayatollahi, Azin , Variji, Zeinab ,

Introduction: Beckers’s nevus is a cutaneous hamartoma which usually appears as a circumscribed hyperpigmentation with hypertrichosis. It usually presents unilaterally and the usual site is shoulder and scapula. It is rarely congenital and it is usually noticed first during adolescence. Case Report: Herein, we report a congenital bilateral large Becker’s nevus with positive familial history ...

2016
Khaled Abdulmoneim Gadalla

Objectives: To evaluate the factors that affect the success rate of ESWL for treatment of renal stones and to estimate the prevalence of stone recurrence during a 1-year period. Materials and Methods: During the period of January, 2010 and December, 2010, prospective study of 142 subjects with single or multiple renal stones (<30 mm, largest diameter) undergone ESWL monotherapyby SiemensLITHOSK...

Introduction: Intraoral synechia is a rare congenital condition, generally associated with other maxillo-facial malformations. We present a neonate with congenital intraoral bilateral synechia without any other facial anomalies.   Case Report: In this paper, we present a 19-day-old male neonate with congenital intraoral bilateral synechia without any other facial anomalies. We review the litera...

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