Prune Belly Syndrome Detailed information on prune belly syndrome, including causes, symptoms, diagnosis,and treatment. http://www.healthsystem.virginia.edu/uvahealth/peds_urology/pbs.cfm
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Birth Disorder Information Directory - P prune belly syndrome (Abdominal Muscle Absence/Aplasia/Deficiency/DefectAnomalad/Syndrome, Eagle Barrett Syndrome, Fröhlich Syndrome, Obrinsky Syndrome, http://www.bdid.com/defectp.htm
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AllRefer Health - Prune Belly Syndrome (Eagle-Barrett Syndrome) prune belly syndrome (EagleBarrett Syndrome) information center covers causes,prevention, symptoms, diagnosis, treatment, incidence, risk factors, signs, http://health.allrefer.com/health/prune-belly-syndrome-info.html
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Extractions: helpful? yes no Prune Belly syndrome: Eagle Barrett syndrome Prune Belly syndrome is an extremely rare condition which, in most cases, affects males. It is characterised by a triad of distinctive features including weak or missing abdominal muscles, an abnormal expanded bladder and problems in the upper urinary tract which may include the bladder, ureters and kidneys and, in most males, bilateral cryptorchidism (failure of both testes to descend in the scrotum). Prune Belly syndrome affects indviduals to varying degrees. The prognosis may be serious and often life-threatening including in utero death, stillbirth or death within the first few weeks of life. Alternatively, the prognosis may involve a combination of congenital anomalies in infancy. For others, the outcome may be a near-normal life expectancy, with varying degrees of urinary tract pathology. As the name implies, Prune Belly syndrome is characterised by an abdomen with a wrinkly or 'prune-like' appearance with multiple folds of skin. The cause of this is a blockage in a part of the unborn's urinary tract, resulting in other parts of the tract developing abnormally. The obstruction may occur in the urethra (the tube that drains urine from the bladder to the outside of the body for elimination). The effect of this is that the urine 'reverse flows', causing an expanded bladder. Fluid subsequently develops in the abdomen which stretches larger and larger. The fluid is reabsorbed before birth and when the infant is born, it has a sagging or wrinkled abdomen (thus the 'prune belly' name). Infants may have a range of severity from a complete absence of musculature to an abdomen of normal appearance. Infants may have difficulties in sitting upright.
Prune Belly Syndrome National prune belly syndrome Association 30 Salem Blvd. Naugatuck, CT 06770Phone (203) 7296054 contact Brian Beirne E-mail bbeirne@healthcon.com http://www.kumc.edu/gec/support/prunbely.html
Genitourinary And Kidney Disorders - Prune Belly Syndrome The cause of prune belly syndrome is unknown, however, some cases have been If your child has mild prune belly syndrome, he/she may be maintained on http://www.schneiderchildrenshospital.org/peds_html_fixed/peds/urology/pbs.htm
Extractions: an abnormal, expanded bladder and problems in the upper urinary tract, which may include the bladder, ureters, and kidneys Because of the substantial involvement of the urinary tract, children with prune belly syndrome are usually unable to completely empty their bladders and have serious bladder, ureter, and kidney impairment. A child with prune belly syndrome may also have other birth defects. Most commonly, these defects involve the skeletal system, intestines, and heart. Girls may have defects in their external genitalia, as well. Some infants who have prune belly syndrome may be stillborn or die within a few months of birth. What causes prune belly syndrome?
Extractions: n. Congenital absence of abdominal muscles, in which the outline of the intestines is visible through the protruding abdominal wall and the skin in the abdominal region is wrinkled. Also called prune-belly syndrome triad syndrome Wikipedia Prune belly syndrome Prune belly syndrome is a rare birth defect affecting about 1 in 35,000 births. About 96% of those affected are male. Prune belly syndrome is a congenital disorder of the urinary system , characterized by a triad of symptoms. The syndrome is named for the mass of wrinkled skin that is often (but not always) present on the abdomens of those with the disorder. Other names for the syndrome include Abdominal Muscle Deficiency Syndrome, Congenital Absence of the Abdominal Muscles, Eagle-Barrett Syndrome, and Obrinsky Syndrome. Prune belly syndrome is often diagnosed via ultrasound while a child is still in-utero. An abnormally large abdominal mass is the key indicator, as the abdomen swells with the pressure of accumulated urine. In young children, frequent
Prune Belly Syndrome Links to information and resources for prune belly syndrome (EagleBarrett syndrome). http://rarediseases.about.com/cs/prunebellysynd/
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Prune Belly Syndrome Prune Belly Syndrome, also known as Eagle - Barrett Syndrome, is a rare disordercharacterized by partial http://my.webmd.com/hw/health_guide_atoz/nord478.asp
Extractions: Prune-Belly syndrome, also known as Eagle-Barrett syndrome, is a rare disorder characterized by partial or complete absence of the stomach (abdominal) muscles, failure of both testes to descend into the scrotum (bilateral cryptorchidism), and/or urinary tract malformations. The urinary malformations may include abnormal widening (dilation) of the tubes that bring urine to the bladder (ureters), accumulation of urine in the ureters (hydroureter) and the kidneys (hydronephrosis), and/or backflow of urine from the bladder into the ureters (vesicoureteral reflux). Complications associated with Prune-Belly syndrome may include underdevelopment of the lungs (pulmonary hypoplasia) and/or chronic renal failure. The exact cause of Prune-Belly syndrome is not known.
Prune Belly Syndrome - Wikipedia, The Free Encyclopedia prune belly syndrome is a rare birth defect affecting about 1 in 40000 births . prune belly syndrome is often diagnosed via ultrasound while a child is http://en.wikipedia.org/wiki/Prune_belly_syndrome
Extractions: You did it! Over US$240,000 was donated in the 21 day fund drive. Thank you for your generosity! You are still welcome to make a donation or purchase Wikimedia merchandise Prune belly syndrome is a rare birth defect affecting about 1 in 40,000 births. About 96% of those affected are male. Prune belly syndrome is a congenital disorder of the urinary system , characterized by a triad of symptoms. The syndrome is named for the mass of wrinkled skin that is often (but not always) present on the abdomens of those with the disorder. Other names for the syndrome include Abdominal Muscle Deficiency Syndrome, Congenital Absence of the Abdominal Muscles, Eagle-Barrett Syndrome, and Obrinsky Syndrome. edit edit Prune belly syndrome is often diagnosed via ultrasound while a child is still in-utero. An abnormally large abdominal mass is the key indicator, as the abdomen swells with the pressure of accumulated urine. In young children, frequent
Genitourinary And Kidney Disorders - Prune Belly Syndrome prune belly syndrome is also known as triad syndrome or EagleBarrett syndrome . Specific treatment for prune belly syndrome will be determined by your http://uuhsc.utah.edu/healthinfo/pediatric/urology/pbs.htm
Extractions: an abnormal, expanded bladder and problems in the upper urinary tract, which may include the bladder, ureters, and kidneys Because of the substantial involvement of the urinary tract, children with prune belly syndrome are usually unable to completely empty their bladders and have serious bladder, ureter, and kidney impairment. A child with prune belly syndrome may also have other birth defects. Most commonly, these defects involve the skeletal system, intestines, and heart. Girls may have defects in their external genitalia, as well. Some infants who have prune belly syndrome may be stillborn or die within a few months of birth. What causes prune belly syndrome?
Prune Belly Syndrome Medical Information prune belly syndrome Information from Drugs.com. prune belly syndrome is agroup of congenital anomalies characterized by three major findings http://www.drugs.com/enc/prune_belly_syndrome.html
Extractions: Advanced Search Or click the first letter of a drug name: A B C D ... Z Injury Disease Nutrition Poison ... Abdominal muscles Prune belly syndrome is a group of congenital anomalies characterized by three major findings: Eagle-Barrett syndrome The underlying causes of prune belly syndrome are unknown. 96-97% of cases are boys. Expectant mothers carrying affected infants may develop varying degrees of oligohydramnios (insufficient amniotic fluid ) that make it likely the infant will have lung problems. (See also
UNSW Embryology-OMIM PRUNE BELLY SYNDROME The appellation prune belly syndrome is descriptive because the intestinal (1982) reported 2 brothers and a sister with prune belly syndrome with http://embryology.med.unsw.edu.au/OMIMfind/kidney/OMIM-100100.htm
Extractions: DEVELOPMENT OF THE URINARY SYSTEM Embryology Home Page Online Mendelian Inheritance in Man (Internet Link) This page is for computers without external internet access. Back to UNSW Embryology-Kidney Notes List of OMIM search results TEXT REFERENCES SEE ALSO CREATION DATE ... "16 MEDLINE Citations" Note: pressing the symbol will find the citations in MEDLINE whose text most closely matches the text of the preceding OMIM paragraph, using the Entrez MEDLINE neighboring function. This condition was first described by Frolich (1839) . The appellation 'prune belly syndrome' is descriptive because the intestinal pattern is evident through the thin, lax, protruding abdominal wall in the infant ( Osler, 1901
UNSW Embryology-OMIM PRUNE BELLY SYNDROME 264140 prune belly syndrome WITH PULMONIC STENOSIS, MENTAL RETARDATION, AND DEAFNESS.TABLE OF CONTENTS. TEXT; REFERENCES; CREATION DATE; EDIT HISTORY http://embryology.med.unsw.edu.au/OMIMfind/kidney/OMIM-264140.htm
Extractions: DEVELOPMENT OF THE URINARY SYSTEM Embryology Home Page Online Mendelian Inheritance in Man (Internet Link) This page is for computers without external internet access. Back to UNSW Embryology-Kidney Notes List of OMIM search results TEXT REFERENCES CREATION DATE EDIT HISTORY ... "1 MEDLINE Citation" Lockhart et al. (1979) described a family in which 2 brothers and a sister had this combination. A fourth sib may have been affected; the mother reported that the male, who died 25 hours after birth, had 'a big bladder, big ureters, bad kidneys.' The hearing loss was sensorineural in nature. Because the involvement in the female was less marked than in the males, the possibility of X-linked inheritance was suggested. No information concerning abnormalities in the mother was provided. 1. Lockhart, J. L.; Reeve, H. R.; Bredael, J. J.; Krueger, R. P. :
UrologyHealth.org Glossary: Prune Belly Syndrome prune belly syndrome. A triad of congenital symptoms that include multiple tractabnormalities. The common abnormalities include the absence of abdominal http://www.urologyhealth.org/glossary/popup.cfm?id=969
► Prune Belly Syndrome A medical encycopedia article on the topic prune belly syndrome. http://www.umm.edu/ency/article/001269.htm
Extractions: Causes, incidence, and risk factors: The underlying causes of prune belly syndrome are unknown. There is blockage to the flow of urine from the kidney to the outside of the body during fetal life. For example, dilatation of the urinary tract may develop as a result of urethral obstruction in the womb. The incidence is approximately 1 in 30,000 to 40,000 births. Boys are almost solely affected.
Prune Belly Syndrome PruneBelly Syndrome, also known as Eagle-Barrett Syndrome, is a rare disordercharacterized by partial or complete absence of the stomach (abdominal) http://www.bchealthguide.org/kbase/nord/nord478.htm
Extractions: It is possible that the main title of the report Prune Belly Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Prune-Belly Syndrome, also known as Eagle-Barrett Syndrome, is a rare disorder characterized by partial or complete absence of the stomach (abdominal) muscles, failure of both testes to descend into the scrotum (bilateral cryptorchidism), and/or urinary tract malformations, such as abnormal widening (dilation) of the tubes that bring urine to the bladder (ureters), accumulation of urine in the ureters (hydroureter) and the kidneys (hydronephrosis), and/or backflow of urine from the bladder into the ureters (vesicoureteral reflux). Complications associated with Prune-Belly Syndrome may include underdevelopment of the lungs (pulmonary hypoplasia) and/or chronic renal failure. The exact cause of Prune-Belly Syndrome is not known. National Prune Belly Syndrome Network
