Pierre-Robin Syndrome pierrerobin syndrome. This article submitted by Indiana Parent InformationNetwo on 1/31/97. Author's Email ipin@indy.net looking http://neuro-www.mgh.harvard.edu/neurowebforum/GeneralFeedbackArticles/1.31.9712
Pierre Robin, Syndrome : Arborescences MeSH Translate this page pierre robin, syndrome. pierre robin, syndrome C05.500.460.606 page CISMeFdu motclef prognathisme C05.500.460.655 page CISMeF du motclef http://www.chu-rouen.fr/navimesh/navipierrerobinsyndrome.html
Robin's Syndrome (www.whonamedit.com) the tongue, and an absent gag reflex. Also known as pierre robinssyndrome,robin's anomalad,robins sequence. Who named it? http://www.whonamedit.com/synd.cfm/1291.html
Extractions: A very rare congenital malformation syndrome characterized by unusual smallness of the jaw combined with cleft palate, downward displacement of the tongue, and an absent gag reflex. The affected child is in serious danger because of difficulty in breathing and feeding. The abnormality may occur in isolation or as a variable component of many genetic syndromes. Inheritance is autosomal recessive.
Pierre Robin (www.whonamedit.com) pierre robin French dental surgeon, 18671950. Associatedwith robin's syndrome,Stickler's syndrome. Who named it? http://www.whonamedit.com/doctor.cfm/1233.html
Extractions: Pierre Robin, in his time the doyen of French dental surgeons, was best known for his contributions to orthodentistry, but published on many aspects of dentistry and oral hygiene. His main interest was glossoptisis, on which he wrote more than 20 articles and a monograph. He was professor at the French School of Stomatology, and from 1914, with Nogue, he was editor-in-chief of the Revue de Stomatologie.
Intubation Et Syndrome De Pierre Robin Translate this page INTUBATION D'UN ENFANT DE UN MOIS, PORTEUR D'UN syndrome DE pierre robin.F. Semjen, A Didier. Hôpital des Enfants - CHU de Bordeaux. http://www.airwaysud.com/cas_e_5/cas.htm
Extractions: INTUBATION D'UN ENFANT DE UN MOIS, PORTEUR D'UN SYNDROME DE PIERRE ROBIN L'association d'un par hypoplasie mandibulaire et d'une fente palatine Choisissez-vous une intubation : Une induction par voie intraveineuse Vous faites une laryngoscopie directe pour intuber Vous effectuez une intubation fibroscopique Que faites-vous pour faciliter le geste? ... Retour Menu
Le Syndrome De Pierre-Robin Translate this page robin. Maladies rares. Le syndrome de pierre-robin. Chaque année,un enfant sur 8 000 naît porteur dun syndrome de pierre-robin. http://www.essentielsante.net/Html/MaladiesRares/cadre/120060400.htm
Pierre Robin PO Box 11082, * Chattanooga, TN 37401. 800, 332-2373. pierre robin.What is pierre robin? pierre robin is not a syndrome or a disease. http://www.faces-cranio.org/Disord/PierreRobin.htm
Extractions: The National Craniofacial Association P. O. Box 11082 * Chattanooga, TN 37401 Pierre Robin What is Pierre Robin? Pierre Robin is not a syndrome or a disease. It is usually referred to as Pierre Robin Sequence, although it is also know as "Pierre Robin Malformation Sequence", "Robin Anomalad", and "Cleft Palate, Micrognathia and Glossoptosis." It is the name given to the following birth defects if they appear together: Why did this happen? Doctos do no know exactly why Pierre Robin occurs. They do not believe it is the result of anything the mother did or did not do during pregnancy. Will this happen to children I have in the future? Pierre Robin does not tend to run in families. The chances of you having another child with Pierre Robin are very small. What kinds of problems could my child have? In addition to the physical characteristics common to Pierre Robin, your child may have the following problems:
Pierre Robin Sequence/Syndrome Frequently Asked Questions About pierre robin Sequence/syndrome. Whatis pierre robin Sequence? This is a condition named after the http://www.jpanchal.com/PierreRobinSequenceSyndrome.htm
Extractions: What are the Special Concerns with Pierre Robin? The infant with Pierre Robin Sequence will get better over time. While we wait for your baby to grow stronger, certain supportive care measures will be required. The most important aspect of care for your baby is to assure that breathing is adequate. Various supports for opening the breathing passages may be necessary. These include a soft plastic tube placed into the windpipe, a tube through the nostril past the back of the tongue, and positioning the baby on the abdomen or side. Most care, including diaper changes, feedings, and baths, will be done while your baby is lying on the tummy. How Long Will My Baby Be in the Hospital? The length of the hospital stay depends upon how severe the breathing and feeding problems are. The infants must have their breathing monitored until obstructions are no longer as frequent or severe as in the immediate newborn period. Your baby may be discharged with the feeding tube in place. You will be taught how to manage the tube and the bottle feedings and will have plenty of time to practice. Your baby will also go home with a monitor which will sound an alarm if your baby has trouble breathing while at home.
Page 2 pierrerobin syndrome/Sequence Garland Neal's PRS Story pierre robinNetwork National Organization of Rare Disorders Ped Database. http://members.tripod.com/~Craniofacial/page2.htm
Extractions: The Craniofacial Disorders indexed on this page are: Jackson-Weiss, Langer-Geidon, Parry-Rombergs, Pfeiffer, Pierre-Robin, Russell-Silver, Saethre-Chotzen, Sagittal Synostosis, Shprintzen-Goldberg, Stickler, and Treacher-Collins. Page 1 includes Antley-Bixler, Apert, Arhinia, Baller-Gerold, Carpenter, Craniosynostosis, Crouzon and Goodman. Jackson-Weiss
Lycos MultiMania Pages Perso - Hébergement Gratuit syndrome de pierre robin, Aide. syndrome DE pierrerobin, http//membres.lycos.fr/pierrevandaele/. Forum administré http://forums.multimania.lycos.fr/use/tremplin/46459/index.phtml
Extractions: Sujet Auteur Date pierre robin et déficit auditif un visiteur RE: pierre robin et déficit auditif Pierre Vandaele conseils pratiques un visiteur RE: conseils pratiques un visiteur RE: conseils pratiques Pierre Vandaele pierre robin et allaitement un visiteur RE: pierre robin et allaitement Pierre Vandaele tetine pierre robin avec aillette un visiteur RE: tetine pierre robin avec aillette Pierre Vandaele Chirurgien Plasticien pédiatrique...
PIERRE ROBINS SEQUENCE congestive heart failure. · 40% of infants with pierre robin haveStickler syndrome (see additional information). · 15% of infants http://www.forwardface.org/misc_text/conditions/robins.htm
Extractions: PIERRE ROBIN SEQUENCE (PRS) Pierre Robin is a sequence instead of a syndrome because it is caused by a series of events that take place in fetal development. Beginning with a defect of the lower fetal jaw (abnormally small jaw or micrognathia), the tongue becomes abnormally placed in the back of the throat ( glossoptosis ) and, in turn, causes a cleft palate (hole in the roof of the mouth). The too small lower jaw does not leave room to accommodate the tongue. The tongue therefore accommodates by forming farther back and higher up in the mouth. Not only does this placement of the tongue inhibit the airways, it also prevents the full closure of the developing soft palate; hence the cleft. Infants with breathing difficulties as a result of tongue placement, also have difficulty swallowing (dysphagia). With swallowing problematic, these children often fail to thrive and may even temporarily stop breathing. In turn, these breathing problems could lead to enlargement of part of the heart, lung malfunctioning, high blood pressure and even congestive heart failure. Pierre Robin sequence occurs in 1:8,000 live births with the cause being either genetic or external.
Hannah Isabella Snyder Diagnosis pierrerobin syndrome Also had Spastic Quadriplegia, Cerebral Palsy, Hydrocephalus,Panhypopituitarism Hypothyroidism, Neurofibromatosis and Seizures http://www.kidsneedprayer.net/hannah_s.html
Extractions: Corey has written a book about how he feels about his sister dying and he did a very good job. Please pray that we can get this book published I believe that it will be helpful to kids and adults. God willing we will get it out there City/State: Alexander, NC Diagnosis: Pierre-Robin Syndrome Also had Spastic Quadriplegia, Cerebral Palsy, Hydrocephalus, Panhypopituitarism Hypothyroidism, Neurofibromatosis and Seizures, Heart and Respiratory Problems Age: 3 Years Old
PRN Fact Sheet pierre robin Network. Fact Sheet. pierre robin Network (PRN) is a not for profitgroup for those who have a common interest in pierre robin Sequence. http://www.pierrerobin.org/PRNFactSheet.htm
Extractions: Home Ab out Us What's New here ... Stickler Syndrome Stories to Share Our Kids' Stories Adult Stories Tips from our Parents Safety Tips Trach Tips Cleft Repair - coming soon Jaw Distraction - coming soon G-tube - coming soon Pierre Robin Network Fact Sheet Pierre Robin Network (PRN) is a not for profit group for those who have a common interest in Pierre Robin Sequence. We are parents of children with PRS, caregivers, adults with PRS and medical professionals. We network with each other to provide support to each other and educate ourselves about PRS and the issues it brings with it. We share our experiences. We do not offer medical advice, please contact your health care provider for all medical advice. The goal of our group is to reach as many people as possible and allow them to network with each other. There is not much information available about PRS, we want to change that. Pierre Robin Sequence was first discovered in 1923 by physician Pierre Robin. Characteristics generally include micrognathia (small jaw), cleft palate, glossoptosis (downward placed tongue) and airway obstruction. The chin is recessed which causes the tongue to fall back and obstruct the airway. PRS children should be seen by an experienced craniofacial or cleft palate team, in addition to the pediatrician. PRS can be secondary to other conditions and we feel it is best to have every child with PRS seen by a pediatric geneticist to check for any other conditions.
Extractions: fente palatine 1. Wheatley RS, Stainthorp SF. Intubation of a one-day-old baby with the Pierre-Robin syndrome via a laryngeal mask. Anaesthesia 1994;49:733 2. Hansen TG, Joensen H, Henneberg SW et al. Laryngeal mask airway guided tracheal intubation in a neonate with the Pierre Robin syndrome. Acta Anaesthsiol Scand 1995;39:129-131
Articles From LEAVEN: Pierre Robin Sequence There are over 180 other abnormalities associated with Velocardio-facialsyndrome (pierre robin Network 2001). How Leaders Can Help. http://www.lalecheleague.org/llleaderweb/LV/LVOctNov01p111.html
Extractions: From: L EAVEN , Vol. 37 No. 5, October-November 2001, pp. 111-112. It is eight o'clock in the morning and you have just served breakfast to your children when the phone rings. Answering the phone, you hear a tearful mother on the other end: "My baby has just been diagnosed with Pierre Robin Sequence. Can you help me? Will I still be able to breastfeed?" As La Leche League Leaders accustomed to helping mostly healthy mothers and babies work through common breastfeeding difficulties, this question might leave many of us speechless and scrambling for information. Although encountered rarely, Pierre Robin Sequence has its own implications for breastfeeding and infant care, making it important for Leaders to have a basic understanding of the condition. What is Pierre Robin Sequence?
Extractions: Pierre Vandaele Syndrome de Pierre Robin par le Dr Véronique Abadi e Extrait de l'ouvrage "112 maladies génétiques, maladies rares" édité par Allo-Gènes, Centre national d'information sur les maladies génétiques, sous la direction du Pr Marie-Louise Briard, grâce au soutien financier de la CNAMTS. Sommaire : Définition clinique Evolution Génétique Géne ... Glossaire Définition clinique Le syndrome de Pierre Robin se définit par l'association d'une fente palatine postérieure romane médiane, d'un rétrognathisme et d'une glossoptose . Les trois éléments de la triade sont liés entre eux par un lien de cause à effet. Sa dénomination rappelle la description faite par Pierre Robin, dans les années 20, de nourrissons atteints de détresse respiratoire obstructive par glossoptose et rétromandibulie. Au moment de la croissance anatomique de la cavité orale de l'embryon, la fente se constitue en raison de la persistance de la langue en position verticale lors de la fusion antéropostérieure et latéromédiane des processus palatins secondaires, au cours de la 7e semaine de vie intra-utérine. La langue reste en position verticale postérieure du fait de l'insuffisance de tonus de sa base et d'un défaut de croissance de la mandibule. Ce
Listings Of The World Health Conditions And Diseases Rare Listings World Health Conditions and Diseases Rare Disorders PierreRobin syndrome. Listings World, Over 2 million http://listingsworld.com/Health/Conditions_and_Diseases/Rare_Disorders/Pierre_Ro
Katalog - Wirtualna Polska Serwis Katalog w Wirtualna Polska S.A. pierwszy portal w Polsce. http://katalog.wp.pl/DMOZ/Health/Conditions_and_Diseases/Rare_Disorders/Pierre_R
