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         Prune Belly Syndrome:     more detail
  1. Prune-belly syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by David, MD Greenberg, 2005

21. 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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      Prune Belly Syndrome
      What is prune belly syndrome?
      Prune belly syndrome is also known as triad syndrome or Eagle-Barrett syndrome. It is characterized by a triad of abnormalities that include the following:
      • absence of abdominal muscles
        undescended testicles - a condition seen in newborns whereby one (or both) of the male testes has not passed down into the scrotal sac
        an abnormal, expanded bladder and problems in the upper urinary tract, which may include the bladder, ureters, and kidneys

22. Prune Belly Syndrome
prune belly syndrome (EagleBarrett Syndrome, Fröhlich Syndrome, Obrinsky Syndrome).prune belly syndrome prune belly syndrome Short description of cell
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23. Birth Disorder Information Directory - P
prune belly syndrome (Abdominal Muscle Absence/Aplasia/Deficiency/DefectAnomalad/Syndrome, Eagle Barrett Syndrome, Fröhlich Syndrome, Obrinsky Syndrome,
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24. 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,
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Alternate Names : Eagle-Barrett Syndrome Definition Prune belly syndrome is a group of congenital anomalies characterized by three major findings:
  • Deficient development of abdominal muscles (causing the skin of the abdomen to wrinkle like a prune) Undescended testicle Urinary tract anomalies

Abdominal Muscles 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

25. AllRefer Health - Prune Belly Syndrome Prognosis (Expectations) (Eagle-Barrett S
prune belly syndrome (EagleBarrett Syndrome) information center coversPrognosis (Expectations).
http://health.allrefer.com/health/prune-belly-syndrome-prognosis.html

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Alternate Names : Eagle-Barrett Syndrome Prune Belly Syndrome Prognosis (Expectations) Prune Belly Syndrome is a serious and often life threatening problem. Many newborns survive with varying degree of chronic problems, but others are stillborn or die in the first two years of life.
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Prune Belly Syndrome Prognosis Prune Belly Syndrome Complications Calling Your Health Care Provider Topics that might be of interest to you Chronic Renal Failure Potter Syndrome Undescended Testicle Urinary Tract Infection ... Intravenous Pyelogram Other Topics Amniotic Fluid Stillbirth Review Date : 11/3/2003 Main Page of Prune Belly Syndrome From Our Sponsors: A.D.A.M., Inc. is accredited by URAC, also known as the American Accreditation HealthCare Commission (www.urac.org). URAC's

26. PRUNE BELLY SYNDROME: Contact A Family - For Families With Disabled Children: I
Contact a Family is a UK charity for families with disabled children. We offerinformation on specific conditions and rare disorders.
http://www.cafamily.org.uk/Direct/p505.html
printer friendly PRUNE BELLY SYNDROME home how we can help medical information index of conditions ... how you can help Did you find this page
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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.

27. 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
Prune Belly syndrome
National Prune Belly Syndrome Association
30 Salem Blvd. Naugatuck, CT 06770 Phone: (203) 729-6054 contact: Brian Beirne E-mail: bbeirne@healthcon.com
Web site URL: http://healthcon.com
GUMS (Guardians/Grandparents United for Moral Support)
c/o Joyce Henderson 4512 Wilcox Pl. Jamesville, NY 13078 Phone: (315) 492-0090
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28. 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
Genitourinary and Kidney Disorders
Prune Belly Syndrome
What is prune belly syndrome?
Prune belly syndrome is also known as triad syndrome or Eagle-Barrett syndrome. It is characterized by a triad of abnormalities that include the following:
  • absence of abdominal muscles
    undescended testicles - a condition seen in newborns whereby one (or both) of the male testes has not passed down into the scrotal sac
    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?

29. Prune Belly Syndrome: Definition And Much More From Answers.com
abdominal muscle deficiency syndrome n. Congenital absence of abdominal muscles,in which the outline of the intestines is visible through the.
http://www.answers.com/topic/prune-belly-syndrome
showHide_TellMeAbout2('false'); Business Entertainment Games Health ... More... On this page: Medical Wikipedia Mentioned In Or search: - The Web - Images - News - Blogs - Shopping Prune belly syndrome Medical abdominal muscle deficiency syndrome
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.
Symptoms
Diagnosis
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

30. Prune Belly Syndrome
Links to information and resources for prune belly syndrome (EagleBarrett syndrome).
http://rarediseases.about.com/cs/prunebellysynd/
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Guide picks Also known as Eagle-Barrett or triad syndrome, a disorder affecting the urinary tract, abdominal muscles, and male testes.
Prune Belly Syndrome

Article looks at the symptoms, diagnosis, and treatment of prune belly syndrome. From the About.com Guide to Rare/Orphan Diseases. Prune Belly Syndrome Network
Site offers information, support forum, patient registry, and links. MEDLINEplus Health Information
Basic information and links about Prune Belly syndrome. Medical Center of Central Georgia
Information about the disorder from the Medical Center of Central Georgia (U.S.). eMedicine: Prune Belly Syndrome
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31. Prune Belly Syndrome
Prune Belly Syndrome, also known as Eagle - Barrett Syndrome, is a rare disordercharacterized by partial
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Who We Are About WebMD Site Map You are in Medical Library Our Content Sources Ask A Question Clinical Trials Health Guide A-Z Health Topics Symptoms Medical Tests Medications ... For a Complete Report Prune Belly Syndrome Important 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. Synonyms
  • Abdominal Muscle Deficiency Syndrome Congenital Absence of the Abdominal Muscles Eagle-Barrett Syndrome Obrinsky Syndrome
Disorder Subdivisions
  • None
General Discussion 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.

32. 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
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Prune belly syndrome
From Wikipedia, the free encyclopedia.
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
Symptoms
edit
Diagnosis
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

33. 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
Prune Belly Syndrome
What is prune belly syndrome?
Prune belly syndrome is also known as triad syndrome or Eagle-Barrett syndrome. It is characterized by a triad of abnormalities that include the following:
  • absence of abdominal muscles
    undescended testicles - a condition seen in newborns whereby one (or both) of the male testes has not passed down into the scrotal sac
    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?

34. 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

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Prune belly syndrome
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Prune belly syndrome
Definition
Prune belly syndrome is a group of congenital anomalies characterized by three major findings:
  • Deficient development of abdominal muscles (causing the skin of the abdomen to wrinkle like a prune) Undescended testicle Urinary tract anomalies
Alternative Names
Eagle-Barrett syndrome
Causes
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

35. 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
UNSW Embryology
DEVELOPMENT OF THE URINARY SYSTEM Embryology Home Page
PRUNE BELLY SYNDROME
Select Entry from OMIM
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
100100 ABDOMINAL MUSCLES, ABSENCE OF, WITH URINARY TRACT ABNORMALITY AND CRYPTORCHIDISM
Alternative titles; symbols
PRUNE BELLY SYNDROME
TABLE OF CONTENTS
  • 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.
    TEXT
    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

36. 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
UNSW Embryology
DEVELOPMENT OF THE URINARY SYSTEM Embryology Home Page
PRUNE BELLY SYNDROME
Select Entry from OMIM
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
264140 PRUNE BELLY SYNDROME WITH PULMONIC STENOSIS, MENTAL RETARDATION, AND DEAFNESS
TABLE OF CONTENTS
  • TEXT REFERENCES CREATION DATE EDIT HISTORY ... "1 MEDLINE Citation"
    TEXT
    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.
    REFERENCES
    1. Lockhart, J. L.; Reeve, H. R.; Bredael, J. J.; Krueger, R. P. :

37. Prune Belly Syndrome Definition - Medical Dictionary Definitions Of Popular Medi
Online Medical Dictionary and glossary with medical definitions.
http://www.medterms.com/script/main/art.asp?articlekey=10446

38. 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

39. ► Prune Belly Syndrome
A medical encycopedia article on the topic prune belly syndrome.
http://www.umm.edu/ency/article/001269.htm
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Prune belly syndrome
Overview Symptoms Treatment Prevention Definition: A disease characterized by three major findings (triad): deficient abdominal muscles (causing the skin of the abdomen to wrinkle like a prune), undescended testicles , and a dilated abnormal urinary tract.
Alternative Names: Eagle-Barrett syndrome
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.
Expectant mothers carrying affected infants may develop varying degrees of oligohydramnios (insufficient amniotic fluid ) that predisposes the infant to lung problems (see Potter syndrome ). The

40. 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
var hwPrint=1;var hwDocHWID="nord478";var hwDocTitle="Prune Belly Syndrome";var hwRank="1";var hwSectionHWID="nord478-Header";var hwSource="en-caQ2_05";var hwDocType="Nord";
National Organization for Rare Disorders, Inc.
Prune Belly Syndrome
Important
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.
Synonyms
  • Abdominal Muscle Deficiency Syndrome Congenital Absence of the Abdominal Muscles Eagle-Barrett Syndrome Obrinsky Syndrome
Disorder Subdivisions
  • None
General Discussion
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.
Resources
National Prune Belly Syndrome Network
PO Box 2125
Evansville, IN 47728-0125

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