61. The National Kidney Research Fund Lee suffers from vater syndrome and has had much to cope with throughout his Lee, like all other children who have vater syndrome suffers from a host of http://www.nkrf.org.uk/pages/news/yhmullett.htm

Other News News Releases 2004 News Releases 2003 News Releases 2002 ... Contact Details NEWS RELEASE 6 December 2002 Lee Mullett from Ipswich is Award winner at National Awards Ceremony 17 year-old Lee Mullet of Ipswich, Suffolk has won the patient category of The National Kidney Research Fund's annual Young Hero Awards. The Young Hero Awards 2002 took place at Planet Hollywood, London on Thursday 28th November. A host of celebrities joined Lee and the other children at the Awards including Christine Hamilton, most recently on television programmes 'I'm a Celebrity Get Me Out of Here' and 'Have I Got News for You', Ben Shephard from GMTV, Jez Edwards and Angelica Bell, children's television presenters, Georgina Sherrington, who plays the Worst Witch, artists from soap opera Emmerdale and children's drama Byker Grove, as well as the Red Arrows. Lee has spent much of his childhood in Great Ormond Street and has recently received his second transplant - his first transplant did not go well, Lee suffered severe complications resulting in the kidney having to be removed. Lee, like all other children who have VATER syndrome suffers from a host of other problems. However, despite his problems and setbacks Lee is a real character. Lee doesn't take no for an answer and when he was twelve years old he signed himself up for the local football team. Lee stayed for three seasons and David's proudest moment was when Lee scored his first goal.

62. Kidney Disorders Board: HealthBoards - HELP! It is sometimes called vater syndrome. You mentioned back, kidney and bowelproblems which are included in vater syndrome. vvertebrae, back http://www.healthboards.com/boards/archive/index.php/t-67493.html

HealthBoards Health Issues Kidney Disorders PDA View Full Version : HELP! 04-06-2002, 11:47 AM 14 yr old girl who has had kidney problems associated with cloaca (birth defect) looking for someone who has the same condition. if you can be some help, please reply. THANX! Magpiezoe 05-10-2002, 03:25 PM Hello, Can you be a little more specific? I have one kidney due to a birth defect plus other complications with it. I used to be very weak. Magpie Magpiezoe 05-10-2002, 03:26 PM Hello, Can you be a little more specific? I have one kidney due to a birth defect plus other complications with it. I used to be very weak. Magpie 05-27-2002, 07:15 PM http://www.healthboards.com/ubb/wave.gif Hi, I saw your post under another list and would like to know if you have heard of vacterl association? It is sometimes called vater syndrome. You mentioned back, kidney and bowel problems which are included in vater syndrome. v-vertebrae, back a-anus, bowel (often including cloaca) c-cardio t-trachea e-esophagus r-renal (kidney) or radius l-limb Even if it is not vacterl (which is just an acronymn for a cluster of birth defects) someone from that group may be able to point you in the right direction. There is a very good support group online with many girls and women from babies on up. Try vaterconnection and go to the message board "mega", post your question and you will probably get replies very soon.

63. Indian Pediatrics - Editorial additional 20% patients had two major defects found in vater syndrome(6).Therefore, FA patient can be easily misdiagnosed as VATER/ VACTERAL syndrome. http://www.indianpediatrics.net/mar2005/mar-285-287.htm

Home Past Issue About IP About IAP ... Subscription Case Reports Indian Pediatrics 2005; 42:285-287 Fanconi’s Anemia in Newborn Tushar B. Parikh Rekha H. Udani Ruchi N. Nanavati Babu Rao V.* Building, KEM Hospital Campus, Parel, Mumbai 400 012, India. Correspondence to: Dr.Tushar B. Parikh, Department of Neonatology, Ward 38, 10th floor, New MSB, KEM Hospital, Parel, Mumbai 400 012, India. E mail: tbparikh@rediffmail.com Manuscript received: March 25, 2004. Initial review completed: Auigust 19, 2004; Revision accepted: September 27, 2004. Abstract: Fanconi’s anemia (FA) is a paradigm for congenital anomalies, aplastic anemia and predisposition to malignancies. Identification of the disease at birth is based on characteristic physical malformations, as hematologic manifestations at birth are extremely rare. We report a case of FA in a newborn who presented with anopthalmia, unilateral radial ray defect, hemivertebrae and thrombo-cytopenia. Key words: Anopthalmia, Fanconi’s anemia (FA), Radial ray defects, Thrombocytopenia.

64. THE MERCK MANUAL, Sec. 5, Ch. 61, Common Hand Disorders Congenital constriction band syndrome involves circumferential constriction of radial club hand and vater syndrome Vertebral defects, imperforate Anus, http://www.merck.com/mrkshared/mmanual/section5/chapter61/61e.jsp

65. REGISTER A GLOBAL USER ACCOUNT who was diagnosed with vater syndrome (also called VATER Association) at birth.vater syndrome causes numerous abnormalities such as the spine http://www.theindependent.com/stories/021705/you_iykwim17.shtml

TheIndependent.com USER REGISTRATION REGISTER A GLOBAL USER ACCOUNT Becoming a registered member is fast and FREE . Just fill out the following information and you'll have access to all the stories on theIndependent.com, including world, regional and local news, professional, college and high school sports and more. To get started fill out the form below. Why Register? Frequently Asked Questions If you previously registered for our free e-mail service or on our Forums, you will need to register for access to the main site. Sign up is as easy as 1, 2, 3! Fields marked require a response Already a Member? Enter your username and password to sign in. Username: Password: (case sensitive) Remember my login Forget Your Password? Reset Your Password. Forget Your Username? Modify Your Account ... Report A Problem Become a Member - Create Account document.writeln(""); ERROR: JavaScript Disabled, please consult your browser's help for information on enabling javascript. Choose a Username: This will be your login or username At least 6 characters No spaces Choose a Password: Must be at least 6 characters Passwords are case sensitive Confirm Password: Password Hint: E-Mail Address: Note: A valid e-mail address is required We will send you an e-mail to verify your registration.

66. Karger Publishers Threedimensional computer reconstruction; vater syndrome bones showmalformation of the stapes (vater syndrome) and the cochlea (trisomy 21). http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowAbstract&ProduktNr=

67. Citation Nr 0427726 Decision Date 10/06/04 Archive Date 10/12 and a condition subsequently identified as VACTERL Syndrome or vater syndrome . this is part of vater syndrome and is not an isolated diagnosis. http://www.va.gov/vetapp04/files3/0427726.txt

68. JUM -- Sign In Page Associated anomalies included vater syndrome (vertebral defects, One fetus (case5) was thought to have vater syndrome (vertebral defects, http://www.jultrasoundmed.org/cgi/content/full/23/6/853

HOME HELP FEEDBACK SUBSCRIPTIONS ... SEARCH QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: This item requires a subscription to Journal of Ultrasound in Medicine Online. Full Text Prenatal Sonographic Diagnosis of Hemivertebra Weisz et al. J Ultrasound Med. This Article Abstract Full Text (PDF) 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 PubMed PubMed Citation Articles by Weisz, B. Articles by Zalel, Y. To view this item, select one of the options below: Sign In User Name Sign in without cookies. Can't get past this page? Help with Cookies. Need to Activate? Password Forgot your user name or password? Purchase Short-Term Access Pay per Article - You may access this article (from the computer you are currently using) for 2 days for US$12.00 Pay for Admission - You may access all content in Journal of Ultrasound in Medicine Online (from the computer you are currently using) for 30 days for US$25.00.

69. URMC Press Release Austin was born with what is called vater syndrome, a group of birth defects Children who have vater syndrome usually are born with at least two of the http://www.urmc.rochester.edu/pr/news/archive/ithaca.html

Press Room Home News Home May 30, 2001 For more information contact: Travis Anderson (716) 273-1757 Ithaca Baby Beats "Condition Incompatible with Life" His family will share its heartwarming story during Miracle Weekend Hours after Austin Lamb was born, doctors at Children's Hospital at Strong in Rochester described the premature baby's condition as grave. Without specialized surgery, the newborn would die. That was in August 2000. Less than a year later, Austin Lamb has undergone four major re-constructive surgeries to make his gastrointestinal system - among other parts of his body - function as it should. His physicians expect him to make a full recovery. As part of its Miracle Weekend celebration May 31 to June 3, Children's Hospital at Strong is honoring five children - including Austin - as Miracle Kids. Each child overcame significant health problems while being treated at Children's Hospital at Strong. Austin's Story On Aug. 16, 2000, some two months before she was due to give birth to her first child, Sally Lamb suddenly went into labor. Because she wasn't due until October, Lamb was transferred from Cayuga Medical Center in Ithaca to Arnot-Ogden Hospital in Elmira, where she delivered a baby boy.

70. Welcome To The TEF / Vater® Web Site! which was abbreviated as vater syndrome (or VATER association) by Quan and This syndrome is also currently being termed as VACTERL, the C referring http://www.tefvater.org/trachea.html

Cardiac Home How The Heart Works PDA = Patent Ductus Arteriosis Coarctation of the Aorta ... TOF = Tetrology of Fallot AVC = Atrioventricular Canal TOA = Transposition of Great Arteries Dextrocardia HPLHS = Hypo-plastic Left Heart Syndrome Pacemaker Cardiac Catheterization Other Heart Defects Congenital Heart Defect or Disease Anal Home IA= Imperforate Anus High Imperforate Anus Low Imperforate Anus Colostomy Ileostomy Jejunostomy Cecumostomy Ace Malone Procedure Bowel Continence Bowel Incontinence Surgeries Radial Home Radial Aplasia Radial Dysplasia Missing Finger or fingers Ulnar defects Multiple Fingers (more than 5) Duplication of Fingers Duplication of Hands Pollicization Operation Ilzarod Operation Hand,arm, leg and foot defects Personal Stories Renal Home Polycystic Kidney Horseshoe kidney Kidney Reflux Ureters Bladder problems UTI- Urinary Tract Infection Bladder Exstrophy Cloaca Cloaca Exstrophy Hypospadia Epispadia Omphacele Testicle problems Male Female Oesophagus Home Oesophageal Atresia First report of EA 1670 First operation Anastamosis of Esophagus Cervical Esophagostomy Gastric Tube Replacement Intercolon Position Gastric Pullup Stretching of Esophagus Dilations of Esophagus Gastrostomy Feeding GERD=Gastro-esophageal Reflux Nissen Fundoplications Medications ... History of Oesophageal Atresia Nursing a baby with Esophageal Atresia Interview about Oesophageal Atresia First Survivors Family Stories

71. Pediatric Pearls vater syndrome (anomalies of vertebrae, anus {imperforate}, tracheosophagealregion and radii); Fanconi’s anemia; congenital thrombocytopenia (TAR syndrome) http://home.coqui.net/myrna/pportho.htm

Pediatric Pearls Orthopedics What entities are associated with absent radii? What is Sprengel’s deformity? Congenital elevation of the scapula is a failure of scapular descent during fetal life, resulting is an elevated, hypoplastic scapula. The affected side of the neck is shorter and fuller and gives the appearance of torticollis. It is associated with congenital scoliosis and renal anomalies. What is the pathophysiology of Osgood-Schlatter disease? The entity consists of painful swelling of one or both tibial tubercles at the insertion of the patellar tendon. The disease is very common in adolescents, usually beginning between the ages of 11 and 15. Vigorous exercise results in stressful pulling of the patellar tendon. Although the tubercles do enlarge from this repetitive strain, the primary problem appears to be a low-grade tendinitis and subsequent new heterophil bone formation in the distal tendon itself. Ossicles have been found in the tendon separate from the tubercle and their removal provides relief. Fortunately, this entity rarely requires surgery. Restriction of activity for two to three weeks and gradual resumption of activity usually diminishes the symptoms. What are the osteochondroses?

72. ICD-9-CM Disease Index: V Vater s ampulla=see condition; vater syndrome 759.89; Vegetation, vegetative.adenoid (nasal fossa) 474.2; consciousness (persistent) 780.03 http://www.dmi.columbia.edu/hripcsak/icd9/2indexv.html

ICD-9-CM Index to Diseases: V Vaccination complication or reaction=see Complications, vaccination not done (contraindicated) V64.0 because of patient's decision V64.2 prophylactic (against) V05.9 arthropod-borne viral disease NEC V05.1 encephalitis V05.0 chicken pox V05.4 cholera (alone) V03.0 with typhoid-paratyphoid (cholera TAB) V06.0 common cold V04.7 diphtheria (alone) V03.5 with poliomyelitis (DTP polio) V06.3 tetanus V06.5 pertussis combined [DTP] V06.1 typhoid-paratyphoid (DTP TAB) V06.2 disease (single) NEC V05.9 bacterial NEC V03.9 specified type NEC V03.89 combination NEC V06.9 specified type NEC V06.8 specified type NEC V05.8 encephalitis, viral, arthropod-borne V05.0 Hemophilus influenzae, type B [Hib] V03.81 hepatitis, viral V05.3 influenza V04.8 with Streptococcus pneumoniae [pneumococcus] V06.6 lileieshmaniasis V05.2 measles (alone) V04.2 with mumps-rubella (MMR) V06.4 mumps (alone) V04.6 with measles and rubella (MMR) V06.4 pertussis alone V03.6 plague V03.3 poliomyelitis V04.0 with diphtheria-tetanus-pertussis (DTP polio) V06.3 rabies V04.5

73. MT Desk: Word Lists - Neonatal Terms VACTERL syndrome; vacuum extraction; vater syndrome (vertebral defects,imperforate anus, WAGR syndrome (Wilms tumor, aniridia, gonadoblastoma, http://www.mtdesk.com/lists_neonatal.shtml

Neonatal Terms Click here to return to the list of word lists. ABO incompatibility ABO hemolytic disease of the newborn ACPS (acrocephalopolysyndactyly) acne neonatorum acrocephaly acrocephalic acrocephalosyndactyly acrocephalopolysyndactyly (ACPS) adiponecrosis subcutanea neonatorum adjusted gestational age AENNS (Albert Einstein Neonatal Developmental Scale) AFP (alpha-fetoprotein) AGA (appropriate for gestational age) AIHA (autoimmune hemolytic anemia) alar flaring Albert Einstein Neonatal Developmental Scale (AENNS) alobar holoprosencephaly alpha-1 antitrypsin deficiency alpha-fetoprotein (AFP) aminophylline amnionic band syndrome ampicillin and gentamicin ("amp&gent") anencephaly aneuploidy aniridia Apgar score APIB (Assessment of Preterm Infant’s Behavior) apnea neonatorum apnea of prematurity appropriate for gestational age (AGA) Apt test arachnodactyly arrhinencephaly Arnold-Chiari deformity Arnold-Chiari malformation Arnold-Chiari syndrome ASD (atrioventricular septal defect) ASD (atrioseptal defect) atrioseptal defect (ASD) atrioventricular septal defect (ASD) autosome Babinski reflex BABYbird II respirator BABYbird II ventilator Babyflex ventilator BAER test (brain stem auditory-evoked response) bag-and-mask ventilation Bair Hugger® warmer blanket - Augustine Medical, Inc.

74. Pediatric Problems - Keep Kids Healthy Sudden Infant Death Syndrome Stuttering. Thyroid gland problems. Tourette syndrome vater syndrome. Vesicoureteral Reflux New! Wilms tumor http://www.keepkidshealthy.com/pediatric_problems.html

Search this site: Advanced Search Site Map Contact Us About Us ... What's New? Main Menu Ask the Pediatrician Useful Tools Index of Topics Pediatric Problems ... Web Links Online Resources What's New Reviews Growth Charts Online Forums ... Height Calculator Newsletters: Subscribe to get free news, tips and updates. Recommend Us tell a friend about us or email this page to a friend Common Problems Diseases/Conditions Common Infections Functional Abdominal Pain Acne Allergies Anemia ... Child Abuse New! Colic Constipation Crossed eyes Dental Health ... Food allergies New! Gastroenteritis Gynecomastia New! Hay fever Headaches Hearing loss Heart murmur ... Suicide New! Sunburn Swimmer's Ear New! Toilet Training Toilet training resistance New! Torticollis Undescended testicles Urinary Tract Infections Vision problems ... Aicardi Syndrome AIDS Anxiety Disorders New! Arrhythmias Arthritis Asperger's syndrome Attention Deficit Hyperactivity Disorder Autism Beckwith Weidemann syndrome ... Celiac Disease New! Cerebral palsy Cleft lip and palate Congenital Adrenal Hyperplasia (CAH) Congenital Heart Disease Craniosynostosis Crohn disease Cystic fibrosis Depression ... Fragile X syndrome Galactosemia Gilberts syndrome Glomerulonephritis Guillain Barre Syndrome Hematuria Hemophilia Hemolytic Uremic Syndrome Henoch-Schonlein purpura Hereditary Hemochromatosis Hirschsprungs disease Horner syndrome Hydrocephalus Hypertension Hypospadias and Chordee Inflammatory bowel disease Irritable Bowel Syndrome New!

75. Medicine Online Medical Reference Medical Information, Symptoms And Signs Medica vater syndrome Support this site is a useful way to get information on where youcan find support if you or a love one is afflicted with vater syndrome. http://www.medicineonline.com/Default.asp?SubCatID=47&Main=1

76. Core Curriculum - POSNA anomalies, hematologic problems, and vater syndrome. Poland s syndrome includeshypoplasia of the pectoralis major. Failure of transverse formation is a http://www.posna.org/index?service=page/coreCurriculum&article=congenitalDeficie

77. Link Directory - Finnish Information Center On Mental Retardation QuanSmith syndrome. VATER ASSOCIATION, OMIM, Victor A. McKusick VACTERL ASSOCIATIONWITH HYDROCEPHALUS, OMIM, Net - Health_Conditions vater syndrome http://www.saunalahti.fi/kup/engl/webs_q.html

Finnish Information Center on Mental Retardation English links A B C D ... Z Qazi-Markouizos syndrome PUERTO RICAN INFANT HYPOTONIA SYNDROME, OMIM, Victor A. McKusick A syndrome of hypotonia, psychomotor retardation, seizures, delayed and dysharmonic skeletal maturation, and congenital fibre type disproportion, Qazi QH, Markouizos D, Rao C, Sheikh T, Beller E, Kula R, J Med Genet. 1994 May;31(5):405-9 - PubMed Qazi markouizos syndrome, Orphanet Quan-Smith syndrome VATER ASSOCIATION, OMIM, Victor A. McKusick VACTERL ASSOCIATION WITH HYDROCEPHALUS, OMIM, Victor A. McKusick PHOSPHATASE AND TENSIN HOMOLOG; PTEN, Victor A. McKusick, Clair A. Francomano et al. VACTERL Association, NORD ... Kaufman's syndrome I (www.whonamedit.com) Quintuple-X syndrome chromosome XXXXX syndrome, Multiple Congenital Anomaly/Mental Retardation (MCA/MR) Syndromes Penta X Syndrome, WebMD X pentasomy: a case and review, Archidiacono N, Rocchi M, Valente M, Filippi G, PubMed Pentasomy X: report of patient and studies of X-inactivation, Funderburk SJ, Valente M, Klisak I, PubMed ... Penta X syndrome: a case report with review of the literature, Kassai R, Hamada I, Furuta H, Cho K, Abe K, Deng HX, Niikawa N, PubMed QM gene and Wilms disease RIBOSOMAL PROTEIN L10; RPL10, OMIM, Victor A. McKusick

78. Christchurch School Of Medicine & Health Sciences, The Developmental Genetics Re The adriamycin–induced rat model of VATER association has presented the opportunity consistent with the vater syndrome with remarkable reproducibility. http://www.chmeds.ac.nz/research/dgrg/projects.htm

Research The Developmental Genetics Research Group People Projects ... Home The Developmental Genetics Research Group Projects Developmental Genetics Some aspects of the embryogenesis of organs derived from the foregut (e.g. oesophagus and trachea) and of the hindgut-cloaca related organs (anorectum, and urogenital tract) are poorly understood. As a consequence, there is an incomplete understanding of the pathomorphogenesis of some of the more common congenital abnormalities requiring surgical correction, such as oesophageal atresia with tracheo-oesophageal fistula (OA-TOF), and anorectal malformations (ARMs). We have been using an adriamycin-induced OA-TOF rat model and an ETU-induced ARMs rat model to look into the embryogenesis and morphogenesis of these congenital malformations. Our studies have shown that development of OA-TOF or ARMs results not only from abnormal septation of the foregut or the cloaca by the tracheo-oesophageal septum and the anorectal septum, respectively, but also from the changes in the normal temporal and spatial patterns of apoptosis (programmed cell death) in the key structures during early embryogenesis. In both models, there was always an abnormal notochord (the notochord is the central organizer during early embryogenesis) despite the use of different teratogens and presence of different congenital malformations.

79. NSF Forums - Post Surgery-SMA Syndrome Reload this Page Post SurgerySMA Syndrome My son had congenital scoliosisthat we have been following since birth (vater syndrome). http://www.scoliosis.org/forum/showthread.php?goto=newpost&t=2262

80. Login Translate this page Skeletal anomalies in the vater syndrome in human embryos. vater syndromehypothesis and report of two further cases. Teratology. http://www.dimed.com/specialista/secure/database/docsmanager/dbidparam/1330.aspx

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