Vater Syndrome Complete online version of The Encyclopaedia of Medical Imaging including textand images from The Encyclopaedia of Medical Imaging s eight book volumes http://www.amershamhealth.com/medcyclopaedia/medical/Volume VII/VATER SYNDROME.a
Share Home - VATER SYNDROME This is part of the vater syndrome. His esophagus wasn t attached to his stomach! . So If you know of someone who was born with the vater syndrome, http://www.shareyourstory.org/webx?230@997.QITBaNgTnHk.0@.eea8485
Extractions: Text Size A A A Front Page ... Rare Disorders : VATER 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)
This Post By SANDRA CHISHOLM There are doctors and plastic surgeons that specialize in vater syndrome. My daughter also has vater syndrome. She has an ear that is deformed. http://tefvater.org/board/VATER with eye and ear defects.html
VATER Association They wanted to know whether or not their children had vater syndrome and This is an example of vater syndrome that will have an excellent quality of http://www.pullthrough.org/ptnn5.html
Extractions: by Alberto Peña, M.D., F.A.C.S., F.A.A.P. Mrs. Michelle Assoian, (former) Director of the Pull-Thru Network, and I, conceived this paper motivated by multiple let ters, requests and phone calls from the parents of children with anorectal malformations who have inquired about the so-called VATER syndrome. Many of them expressed anxiety and confusion regarding this concept. They wanted to know whether or not their children had VATER syndrome and what impact it might have on their child's future. Some parents were confused because their children were labeled as having VATER by some of their doctors and not by others. The word VATER was created from the observation that Vertebral defects, Anal malformations, TE /tracheo-esophageal fistula, E esophageal atresia, Renal defects and Radial bone dysplasia are often seen together in the same child. It is true that many patients with anorectal malformations have associated vertebral, renal, esophageal or radial defects. However, it is our specific purpose to provide orientation to those parents of children with anorectal malformations, to redefine in their own minds what is important and unimpor tant for their children's future. I personally recommend that the concept of VATER be forgotten. To try to label a child with the word VATER has absolutely no relevance from the practical point of view. It has no real, functional prognostic value and tends to complicate a very simple problem.
MUMS List Of Disorders - U - Z vater syndrome or Vacterl Association (80) **; vater syndrome Cloaca Anomaly (1);vater syndrome Goldenhar Syndrome (1) *; vater syndrome Hirschsprung http://www.netnet.net/mums/mum_u-z.htm
Extractions: indicates there is a support group which covers that diagnosis. UPJ Obstruction (4) Uhl Anomaly (Ventricular myocardium, aplasia of right) (1) Ulcerated Colitis (4)* Ullich Disease (1) Ulna Bone, absence, bilateral (arm bone) (3) * Ulna Bone, deficiency (arm bone) (4) * Undescended Testes (72) Undiagnosed (498) Unusual Facies Syndrome (5) Unverricht-Lundborg (Baltic Myoclonus) (1) Ureathra, Diverticulum (1) Ureter Reconstruction (5) Ureterostomy (5) Urethra Fistula (2) Urethra Valve Syndrome (6) Urethra, Diverticulum (1) Urogenital Sinus (2) Urorectal Septum Malformation Sequence (2) Urticaria Pigmentosa (9) Urticaria, Cold (1) Usher Syndrome Type II (1) * Uveitis (pars plantis -dots in vision) (3) * Uvulopalatopharyngoplasty (palate reconstruction) (2) VATER Syndrome or Vacterl Association (80) ** Vaccine Reaction to HIB Vaccine (6) * Vaccine Reaction to Measles Vaccine (9) * Vaccine Reaction to Pertussis (DPT) Vaccine (306) * Vaccine Reaction to Polio Vaccine (5) * Vaccine, Sudden Deafness after Flu vaccine (1)
MUMS List Of Disorders - P Plurelectomy (1); Poisonng, CyanideCausing Brain Damage (1); Poland Syndrome (29)*;Poland Moebius Syndrome (1); Poland vater syndrome (1) http://www.netnet.net/mums/mum_p.htm
Extractions: indicates there is a support group which covers that diagnosis. PANDAS (Ped. Autoimmune Neuropsychiatric Disorders Assoc w/Strep) (1) PEHO Progressive Encephalopathy Edema Hypsarrhythmia Ocular (5) PNET Primary Neuroectodermal Tumor of the Spine (Cancerous) (2) * Pacemaker (heart/cardiac) (23) Pachydermoperiostosis (1) Pachygyria (19) Pachyonychia Congenital (1)* Palate, High (22) Pallister-Hall Syndrome (3) * Pallister-Killian Syndrome (17) ** Pancreatic, Chronic Familial (1) Pancreatitis (7) Panhypogammaglobulinemia (1) Panhypopituitarism (20) Panic-Anxiety Syndrome (1) Panniculitis (inflamed fatty connective tissue in wall of abdomen) (1) Paralyzed Diaphram (4) Paralyzed Palate using palatal obturatur (1) Paramyotonia Congenita (temorary paralysis) (1)* Paranoid Schizophrenia (2) Paraplegia (10) Paris-Trousseau Syndrome 1) Parkes-Weber Syndrome (form of Klippel-Trenaunay) (1) ** Parkinson's (2) Parkinson's, Infantile (1)
Entrez PubMed vater syndrome hypothesis and report of two further cases. LLoyd DJ, McKenzieJ, Kaye HH, Russell G. Two cases are reported of the association of a group http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=7
Entrez PubMed The temporal bone findings of a patient with vater syndrome are reported.The vater syndrome is a no http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=3
Rosser Prune Belly Syndrome, tracheoesophagealfistula associated with vater syndrome, our patient did not have any othercharacteristics of vater syndrome. http://www.duj.com/Article/Rosser2/Potter.html
Extractions: Wake Forest University School of Medicine, Winston-Salem, North Carolina27157 Prune Belly Syndrome, also known as Eagle-Barrett syndrome, is awell known triad of abdominal muscle deficiency or hypoplasia, urinarytract anomalies, and bilateral cryptorchidism. Tracheo-esophagealfistula is a sporadically occurring defect estimated to occur in 1 out4425 live births. Only one case of Prune Belly Syndrome, tracheo-esophagealfistula associated with VATER syndrome, and urethral atresia occurringin the same individual has been reported. We present a uniquecase involving a 33 week fetus with bladder distention and bilateral hydroureteronephrosisdiagnosed in utero who postnatally was diagnosed with Prune Belly Syndrome,tracheo-esophageal fistula, and urethral atresia. CASE REPORT After the placement of a 8 Fr. percutaneous suprapubic tube, a cystogramwas performed which demonstrated a large bladder with severe trabeculation.After instillation of 200 milliliters of cystograffin under gravity, bilateralgrade 5 ureteral reflux was evident by the presence of contrast in therenal pelvis bilaterally On day four of life, the patient was noted to have a creatinine of 1.0mg/dl. Urine output during this time was between 1.5-3 ml/kg/hr. Repeatabdominal ultrasonography demonstrated worsening hydroureteronephrosis.The patient was taken to the operating room for an exploratory laparotomyand urinary diversion. The bladder was noted to have two large
Rosser Reinberg reported the only other case of Prune Belly Syndrome, vater syndrome,and urethral atresia in a stillborn and stated that the urethral atresia http://www.duj.com/Article/Potter.html
Extractions: Wake Forest University School of Medicine, Winston-Salem, North Carolina 27157 Prune Belly Syndrome, also known as Eagle-Barrett syndrome, is a well known triad of abdominal muscle deficiency or hypoplasia, urinary tract anomalies, and bilateral cryptorchidism. Tracheo-esophageal fistula is a sporadically occurring defect estimated to occur in 1 out 4425 live births. Only one case of Prune Belly Syndrome, tracheo-esophageal fistula associated with VATER syndrome, and urethral atresia occurring in the same individual has been reported. We present a unique case involving a 33 week fetus with bladder distention and bilateral hydroureteronephrosis diagnosed in utero who postnatally was diagnosed with Prune Belly Syndrome, tracheo-esophageal fistula, and urethral atresia. CASE REPORT After the placement of a 8 Fr. percutaneous suprapubic tube, a cystogram was performed which demonstrated a large bladder with severe trabeculation. After instillation of 200 milliliters of cystograffin under gravity, bilateral grade 5 ureteral reflux was evident by the presence of contrast in the renal pelvis bilaterally (Figure 1) . Next, abdominal ultrasonography was performed revealing moderate bilateral hydroureteronephrosis, thickened bladder wall, and free intraperitoneal fluid. The patientís initial laboratory results revealed a normal serum creatinine of 0.3 gm/dl. Her postnatal course was complicated by the discovery of free intraabdominal air on day 1 of life. The patient was taken immediately to the operating room where a gastric perforation was discovered secondary to a distal tracheo-esophageal fistula with a proximal pouch. No esophageal atresia was present. The esophagus was ligated and a gastrotomy tube placed.
Extractions: Vol. 112 No. 4, April 1986 Featured Link E-mail Alerts ARTICLE Article Options Send to a Friend Similar articles in this journal Literature Track Add to File Drawer Download to Citation Manager PubMed citation Articles in PubMed by Sakai N Miller RH Contact me when this article is cited N. Sakai, M. Igarashi and R. H. Miller The temporal bone findings of a patient with VATER syndrome are reported. The VATER syndrome is a nonrandom association of anomalies including vertebral, anal, tracheoesophageal, radial, and renal defects. This patient had multiple congenital anomalies: tracheal agenesis with associated laryngoesophageal cleft and tracheoesophageal fistula, tetralogy of Fallot, single umbilical artery, and imperforate anus with cloaca. To our knowledge, there have been no reports of the temporal bone findings in the
Extractions: (advertisement) Home Specialties Resource Centers CME ... Patient Education Articles Images CME Patient Education Advanced Search Consumer Health Link to this site Back to: eMedicine Specialties Plastic Surgery Hand Last Updated: October 21, 2002 Rate this Article Email to a Colleague Synonyms and related keywords: limb anomaly, apical ectodermal ridge, AER, radial dysplasia, constriction bands, Holt-Oram syndrome, VATER syndrome, Fanconi syndrome, TAR syndrome, Aase syndrome, Nager syndrome, Treacher Collins syndrome, Roberts syndrome, intercalated phocomelia, amelia, phocomelia, acheiria, adactyly, absence of hand, absence of fingers, preaxial deficiency, cleft hand, syndactyly, Apert syndrome, Poland syndrome, acrosyndactyly, symphalangism, radioulnar synostosis, flexion deformities, camptodactyly, arthrogryposis, clinodactyly, delta phalanx, duplication, mirror hand, ulnar dimelia, macrodactyly, arthrogryposis multiplex congenita AUTHOR INFORMATION Section 1 of 8 Author Information Embryology And Incidence Dysmorphology Classification ... Bibliography
Extractions: (advertisement) Synonyms, Key Words, and Related Terms: limb anomaly, apical ectodermal ridge, AER, radial dysplasia, constriction bands, Holt-Oram syndrome, VATER syndrome, Fanconi syndrome, TAR syndrome, Aase syndrome, Nager syndrome, Treacher Collins syndrome, Roberts syndrome, intercalated phocomelia, amelia, phocomelia, acheiria, adactyly, absence of hand, absence of fingers, preaxial deficiency, cleft hand, syndactyly, Apert syndrome, Poland syndrome, acrosyndactyly, symphalangism, radioulnar synostosis, flexion deformities, camptodactyly, arthrogryposis, clinodactyly, delta phalanx, duplication, mirror hand, ulnar dimelia, macrodactyly, arthrogryposis multiplex congenita Embryology Limb development takes place during the third to eighth weeks of gestation. The limb buds (ie, Wolff crest) appear as swellings on the ventrolateral aspect of the embryo and are condensations of mesenchyme covered with a thick layer of ectoderm termed the apical ectodermal ridge (AER). The AER is a transient structure that is believed to elaborate morphogens that modulate growth patterns. The underlying mesoderm is organized into a posteriorly located zone of polarizing activity (ZPA) and a progress zone (PZ) more anteriorly. Vessels and then nerves subsequently grow into the limb. Mesodermal differentiation into cartilage and muscle begins to occur. The limb begins to pronate, the elbow flexes, and the hand is flexed and the ulnar deviated.
SECONDARY AORTOESOPHAGEAL FISTULA AS A LETHAL The first case of vater syndrome was described by Quan and Smith in 1973.1 The In 85% of the vater syndrome cases, TEF results from a fistulation of the http://www.kfshrc.edu.sa/annals/213_214/00-138.htm
Extractions: The first case of VATER syndrome was described by Quan and Smith in 1973. The syndrome represents a complex anomaly of skeletal structures and internal organs, an association of vertebral defects with anal atresia, tracheoesophageal fistula (TEF), and radial limb dysplasia. Generally, TEF may occur with or without esophageal atresia. In 85% of the VATER syndrome cases, TEF results from a fistulation of the distal esophagus to the trachea by an atretic proximal blind end of the esophagus. Polyhydramnion and excessive salivation are early clinical manifestations of TEF, followed by choking, coughing and cyanosis after the first feeding. These symptoms can even appear before the first feeding due to a saliva and gastric content aspiration. Therefore, surgical repair of this anomaly within the first 24 hours after delivery presents the treatment of choice and may be of vital importance. Our case report deals with a rare secondary aortoesophageal fistula (AEF) which developed after continuous nasogastric intubation of a child with VATER syndrome, who was operated on for congenital esophageal atresia associated with TEF.
Internet Scientific Publications, LLC. The vater syndrome is first described by a Turkish physician, Prof. Werner W,Beintker M, Schubert J, Kaiser WA The vater syndrome from the urologic http://www.ispub.com/ostia/index.php?xmlFilePath=journals/ijpn/vol4n1/horseshoe.
FOX 11 WLUK: Article vater syndrome July 6, 2005. Fundraising efforts are underway to help save the Hope Marie Anderson has a very rare condition called vater syndrome a http://www.wluk.com/common/article.shtml?article_id=1120658445026900
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