Duplicated Pelvic Floor Musculature and Diastematomyelia in a Cloacal Exstrophy Patient

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منابع مشابه

3-dimensional magnetic resonance imaging modeling of the pelvic floor musculature in classic bladder exstrophy before pelvic osteotomy.

PURPOSE We provide a 3-dimensional (3D) model of the pelvic floor musculature in patients with classic bladder exstrophy using magnetic resonance imaging (MRI). MATERIALS AND METHODS Five male infants 1 day to 12 months old underwent MRI of the pelvis, which was compared to pelvic MRI of 1 male infant without pelvic floor abnormalities. Of the patients 3 were studied before primary closure an...

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Cloacal exstrophy: a complex disease.

INTRODUCTION Cloacal exstrophy is a rare occurrence with an incidence of 1:200,000 to 1:400,000 live births. It represents one of the most challenging reconstructive endeavors faced by pediatric surgeons and urologists. Aside from the genitourinary defects, there are other associated anomalies of the gastrointestinal, musculoskeletal and neurological systems that require a multidisciplinary app...

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Urinary incontinence "as the involuntary loss of urine, which conditions a social and hygienic problem" is defined. There are a variety of techniques for the treatment of urinary incontinence. Our goal is to determine the clinical effectiveness of different methods used to train the musculature of the pelvic floor as treatment for female urinary incontinence, both stress and mixed, and its cont...

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Urea salvage in a neonate with cloacal exstrophy.

Urea kinetics were measured in a child with congenital absence of the colon on days 15, 19, and 23 of age. Urea salvage was 5% of urea production in the first study, increasing to 79% by the third. This provides evidence that the colonic microflora play a more active part in urea salvage than the mucosa and that the establishment of an active lower ileal microflora takes over some of the metabo...

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Y chromosome aberration in a patient with cloacal-bladder exstrophy-epispadias complex: an unusual finding.

Chromosome aberrations or genetic syndromes associated with cloacal-bladder exstrophy complex have rarely been reported. The aim of this report is to describe a 14 year-old female Brazilian patient with a complex urogenital malformation, short stature, lack of secondary se-xual characteristics and Y chromosome aberration. A girl with cloacal bladder exstrophy complex was referred for evaluation...

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ژورنال

عنوان ژورنال: Journal of Radiology Case Reports

سال: 2014

ISSN: 1943-0922

DOI: 10.3941/jrcr.v8i10.2088