MIR Teaching File Case Rs006 Diagnosis prune belly syndrome. Full history. 33year old man with knowndiagnosis of prune belly syndrome and history of multiple prior urinary tract http://gamma.wustl.edu/rs006te181.html
Extractions: Case Author(s): Hamid Latifi,MD , 4/14/95 . Rating: #D2, #Q3 33 year old man with slowly increasing creatinine. Images: Posterior images of abdomen through 20 minutes. Both rows of images are the same but the bottom row is at higher intensity to show the soft tissues. View main image(rs) in a separate image viewer View second image(rs). Post-furosemide posterior images of the abdomen, 5 minutes per frame for 30 minutes. Full history/Diagnosis is available below 33-year old man with known diagnosis of prune belly syndrome and history of multiple prior urinary tract infections who now presents with a slowly increasing serum creatinine. The patient has had a prior vesicostomy. Renal scintigraphy was requested to evaluate relative renal function and exclude renal obstruction. Renal scintigraphy shows a small right kidney with normal left renal function. The collecting systems are dilated bilaterally, worse on the left. The ureters are laterally deviated, which is not unusual in patients with prune belly syndrome. There is no evidence of urodynamically significant obstruction, as documented by prompt clearance of activity from both renal collecting systems after administration of intravenous furosemide. This case simply demonstrates a renal scintigraphic appearance of an adult patient with prune belly syndrome.
Prune Belly Syndrome Home Health Encyclopedia prune belly syndrome it may be possible toprevent it from progressing to prune belly syndrome with prenatal surgery. http://www.healthcentral.com/ency/408/001269prv.html
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Prune Belly Syndrome Home Health Encyclopedia prune belly syndrome skin on abdomen wrinkledlike a prune; undescended testicle; club foot or abnormal limbs are http://www.healthcentral.com/ency/408/001269sym.html
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Geneticalliance.org prune belly syndrome Also known as Eagle Barrett syndrome Support Groups prune belly syndrome Network, Inc. PO Box 2092 Evansville, IN 477280092 http://www.geneticalliance.org/ws_display.asp?filter=support_groups_by_disease&t
Penn State Faculty Research Expertise Database (FRED) , A syndrome characterized by abdominal wall PruneBelly Syndrome, Belly Syndrome, Prune. Belly Syndromes, Prune, Pruneprune belly syndrome. http://fred.hmc.psu.edu/ds/retrieve/fred/meshdescriptor/D011535
Prune Belly Syndrome prune belly syndrome is a serious and often life threatening problem. prune belly syndrome is usually diagnosed before birth or at the time of birth. http://adam.about.com/encyclopedia/001269trt.htm
Extractions: zJs=10 zJs=11 zJs=12 zJs=13 zc(5,'jsc',zJs,9999999,'') zCMt='a00' About Healthcare Center Healthcare Center Essentials ... Surgeries and Procedures zau(256,152,145,'gob','http://z.about.com/5/ad/go.htm?gs='+gs,''); Allergies Arthritis Asthma Breast Cancer ... Help zau(256,140,140,'el','http://z.about.com/0/ip/417/C.htm','');w(xb+xb+' ');zau(256,140,140,'von','http://z.about.com/0/ip/496/6.htm','');w(xb+xb); Search Healthcare Center ENCYCLOPEDIA INDEX Injury Disease Nutrition Poison ... Z Overview Symptoms Treatment Prevention Alternative Names: Eagle-Barrett syndrome Treatment: Expectations (prognosis): 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. Complications: Complications depend on the associated abnormalities. The most common are chronic renal failure and club foot. Calling your health care provider: Prune Belly Syndrome is usually diagnosed before birth or at the time of birth.
Prune Belly Syndrome diagnosis of urinary tract obstruction is made, it may be possible to preventit from progressing to prune belly syndrome with prenatal surgery. http://adam.about.com/encyclopedia/001269prv.htm
Extractions: zJs=10 zJs=11 zJs=12 zJs=13 zc(5,'jsc',zJs,9999999,'') zCMt='a00' About Healthcare Center Healthcare Center Essentials ... Surgeries and Procedures zau(256,152,145,'gob','http://z.about.com/5/ad/go.htm?gs='+gs,''); Allergies Arthritis Asthma Breast Cancer ... Help zau(256,140,140,'el','http://z.about.com/0/ip/417/C.htm','');w(xb+xb+' ');zau(256,140,140,'von','http://z.about.com/0/ip/496/6.htm','');w(xb+xb); Search Healthcare Center ENCYCLOPEDIA INDEX Injury Disease Nutrition Poison ... Z Overview Symptoms Treatment Prevention Alternative Names: Eagle-Barrett syndrome Prevention: There is no known guaranteed prevention. If a prenatal diagnosis of urinary tract obstruction is made, it may be possible to prevent it from progressing to prune belly syndrome with prenatal surgery.
Extractions: This Article Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager ... Cited by other online articles PubMed PubMed Citation Articles by Terada, S Articles by Akasofu, K S Terada, N Suzuki, K Uchide, H Ueno, and K Akasofu BACKGROUND: Prune belly syndrome is a rare and complicated condition affecting the genitourinary organs and abdominal wall. The etiology of abdominal musculature deficiency in prune belly syndrome is controversial. We present a case that should elucidate the etiology of this syndrome. CASE: A spontaneously aborted fetus at 12 weeks' gestation with an early stage of prune belly syndrome was investigated by necropsy and light and electron microscopy. Megalocystis resulting from urethral atresia was diagnosed. There was no hydroureter or hydronephrosis, and both light and electron microscopy demonstrated evidence of development of the abdominal musculature. Both testes were elevated as a result of the megalocystis. CONCLUSION: These findings suggest that hypoplasia of the abdominal musculature and cryptorchidism might develop secondary to the presence of chronic megalocystis in this syndrome.
Prune Belly Syndrome The appellation prune belly syndrome is descriptive because the intestinal Also known as Eagle Barrett syndrome, the prune belly syndrome consists http://ibis-birthdefects.org/start/prunebel.htm
Extractions: 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 ). ( Osler did not use the term "prune belly" ... "In the summer of 1897 a case of remarkable distension of the abdomen was admitted to the wards, with greatly distended bladder, and on my return in September, Dr. Futcher, knowing that I would be interested in it, sent for the child".) The full syndrome probably occurs only in males ... Multiple cases (of the full syndrome) in families have rarely been reported, ... In British Columbia, Baird and MacDonald (1981) found a frequency of 1 in 29,231 live births ... similar to Poland syndrome (173800) in being rather consistently reproduced in many cases but having no clearly demonstrable mendelian basis ...
Prune Belly Syndrome prune belly syndrome Fact Sheet for Specialists in Ukrainian by IBIS. http://ibis-birthdefects.org/start/ukrainian/uprunbel.htm
Extractions: (Prune Belly Syndrome) Cèíîí³ìè: Triad Syndrome; Abdominal Muscle Deficiency Syndrome; Congenital Absence of the Abdominal Muscles; Eagle-Barrett Syndrome. Obrinsky Syndrome. çîâí³øí³é âèãëÿä "Prune Belly", ùî îçíà÷ຠ"æèâ³ò, çìîðùåíèé, ÿê ÷îðíîñëèâ". Ïðè êàòåãî𳿠III - ñïåö³àëüíå ë³êóâàííÿ íåïîòð³áíå. Abdominal Muscles, Absence of, with Urinary Tract Abnormality and Cryptorchidism. Burton BK, Dillard RG. Prune belly syndrome: observations supporting the hypothesis of abdominal overdistention. Am. J. Med. Genet. 1984;17:669-672. Greskovich FJ, Nyberg LM. The Prune belly syndrome: a review of its etiology, defects, treatment and prognosis. J. Urol. 1988;140:707-712. Woodhouse CRJ, Ransley PG, Innes-Williams D. The Prune belly syndrome - report of 47 cases. Arch. Dis. Child. 1982;57:856-859. Ïåðåãëÿíóòî ðåäàêö³éíîþ êîëå㳺þ I.B.I.S.
Karger Publishers 16 Walker J, Prokurat AI, Irving IM prune belly syndrome associated with 17 Adeyokunnu AA, Familusi JB prune belly syndrome in two siblings and a http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowFulltext&ProduktNr=
Extractions: WWW Medical.WebEnds.com Prune-Belly Syndrome; Belly Syndrome, Prune; Belly Syndromes, Prune; Prune Belly Syndromes; Prune-Belly Syndromes; Syndrome, Prune Belly; Syndrome, Prune-Belly; Syndromes, Prune Belly; Syndromes, Prune-Belly A syndrome characterized by abdominal wall musculature deficiency, cryptorchism, and urinary tract abnormalities . The syndrome derives its name from its characteristic distended abdomen with wrinkled skin
Prune Belly Syndrome - Patient UK prune belly syndrome Patient UK. A directory of UK health, disease, illnessand related medical websites that provide patient information. http://www.patient.co.uk/showdoc/40001746/
Extractions: PatientPlus articles are written for doctors and so the language can be technical. However, some people find that they add depth to the articles found in the other sections of this website which are written for non-medical people. Synonyms - Eagle-Barrett syndrome, Abdominal Muscle Deficiency Syndrome, Congenital Absence of the Abdominal Muscles, Obrinsky Syndrome It is a congenital abnormality of unknown aetiology with 3 classic features: Epidemiology
Extractions: 3D Tour of the Vattikuti Institute About the Institute The Vattikuti Institute Prostatectomy Prostate Cancer ... Health Encyclopedia Back to main Health Information page Abdominal muscles Definition: Prune belly syndrome is a group of congenital anomalies characterized by three major findings: Alternative Names: Eagle-Barrett syndrome Causes And Risk: 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 Potter syndrome The newborn infant has a wrinkled abdomen that looks like a prune. This is because the abdomen swelled with fluid in the womb, then lost that fluid after birth, leading to wrinkles of excess skin. The appearance is accentuated by the lack of adequate abdominal musculature. Many infants are either stillborn or die within the first few weeks of life from severe lung or kidney problems, or a combination of congenital anomalies.
Extractions: About Parents Professionals Library ... Research Select Another Subject Adolescent Medicine Arthritis Burns Cardiovascular Disorders Craniofacial Anomalies Dermatology Eye Care Growth and Development High-Risk Newborn High-Risk Pregnancy Infectious Diseases Medical Genetics Mental Health Neurological Disorders Normal Newborn Oncology Orthopaedics Respiratory Disorders Surgery Terminally Ill, Care of Transplantation Urology About Pittsburgh Directions and Parking Departments and Services Find a Doctor ... Genitourinary and Kidney Disorders Online Resources 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: 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.
TOUS: CAS PRUNE BELLY SYNDROME prune belly syndrome . URETHRA . URETHRA, PRUNE BELLYSYNDROME. Total 2 cas cliniques. Sommaire des Index de Radiologie. http://www.med.univ-rennes1.fr/cerf/iconocerf/idx/tous/PRUNE_BELLY_SYNDROME.html
Extractions: Vol Page [Advanced] This Article Submit a response Alert me when this article is cited Alert me when eLetters are posted Alert me if a correction is posted Services Email this link to a friend Similar articles in ADC Online Similar articles in PubMed Alert me to new issues of the journal ... Download to citation manager PubMed PubMed Citation Articles by Woodhouse, C. Articles by Innes-Williams, D CR Woodhouse, PG Ransley and D Innes-Williams Forty-seven cases of prune belly syndrome in children born between 1948 and 1977 are described. They have been classified into three groups according to the state of the urinary tract in the neonatal period. The results achieved in these cases form the basis of our present management. In group I, the most severely affected, early death is inevitable. In group 2 the
Extractions: Text Size A A A Front Page ... Genetic Disorders : Prune Belly Syndrome UF Scientist Finds Unexpected Link Between Cat And Human AIDS Viruses (September 9, 2005) full story Mayo Clinic Develops New Coma Measurement System (September 8, 2005) full story Nitric Oxide Could Extend Fertility (September 8, 2005) Biochemistry , an American Chemical Society journal. full story Flipped, Expelled, Copied, And Shrunk: Researchers Document Dramatic Genome Alterations During Primate Evolution (September 6, 2005) Genome Research presents a series of studies that provide insight into the evolution and variation of primate genomes. The issue will appear online and in print on September 1, concomitant with the publication of the chimpanzee genome sequence in the journal Nature full story Discovery Will Aid Identification Of Misregulated Genes In Rett Syndrome (September 4, 2005) Molecular Cell that the "Rett Syndrome protein", MeCP2, only binds to genes with a specific sequence of nucleotide bases. This knowledge will aid in the identification of the genes that are regulated by the gene MECP2. This work was supported, in part, by the Rett Syndrome Research Foundation (RSRF).
Entrez PubMed prune belly syndrome is a relatively uncommon disorder that is characterized byintrauterine urinary obstruction associated with cryptorchisdism, http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=8