Extractions: Bottling was very difficult, and caused severe respiratory distress, so he got a GT at about a week of age, and never bottled or nursed. Trevor's airway was very fragile and any little thing caused respiratory distress. They tried lots of things including CPAP, but ended up with a vent at a pretty high rate and pressure to keep the airway open. His respiratory doc said the airway was the worst he had ever seen in a child that lived. One thing that we had problems with was keeping the ventilator humidity high enough. At the time, the NICU only had regular vent tubing, and the rainout was severe. At 9 months he moved to M. Children's Chronic Care Program, and they had heated wire vent tubing. The vent humidity was then able to get turned up enough. What this did was keep the mucous thinner, and prevented a lot of episodes with mucous plugs.
Pierre Robin Syndrome Home Up . Click Here! pierre robin syndrome. Click Here! Musice.net Just-recipes.net EnvyMag.com Scholarships-4u.com Shesearch http://www.health-server.com/pierre_robin_syndrome.htm
[DYSPHAGIA] Pediatric Pierre Robin Syndrome Date PrevDate Next Chronological Thread Top DYSPHAGIA Pediatric pierre robin syndrome. Subject DYSPHAGIA Pediatric pierre robin syndrome; http://list.dysphagia.com/dysphagia/1999-May/msg00157.html
[DYSPHAGIA] Pediatric Pierre Robin Syndrome -Reply Date PrevDate Next Chronological Thread Top DYSPHAGIA Pediatric pierre robin syndrome Reply. Subject DYSPHAGIA Pediatric http://list.dysphagia.com/dysphagia/1999-May/msg00146.html
Extractions: Date Prev Date Next [Chronological] [Thread] ... [Top] Subject [DYSPHAGIA] Pediatric Pierre Robin Syndrome -Reply From FriedmaM@allkids.org (Margie Wells-Friedman) Date: Mon, 24 May 1999 09:36:56 -0400 Prev by Date: [DYSPHAGIA] Re: Cleaning nasoendoscopes Next by Date: [DYSPHAGIA] pediatric swallowing problems Index(es): Chronological Thread
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Welcome To AJC! pierre robin syndrome. Causes and Risks. The specific causes of pierre robin syndrome are unknown; it can be part of many genetic syndromes. http://www.ajc.com/health/healthfd/shared/health/adam/ency/article/001607.html
Extractions: Subscribe ... Register Now It's Free! Log in E-mail preferences Site Index Search: Site Yellow Pages Customer care ajc.com Nation/World Metro ... Personals ajc services Archives Advertise online Advertise in print Obituaries ... Sitemap Print edition Today This week A1 image E-mail News Sign up for our Ency. home Disease P Pierre Robin syndrome Overview Symptoms Treatment Prevention Alternative names: Robin sequence Definition: A group of abnormalities marked primarily by a very small lower jaw with a tongue that falls back and downward. The syndrome may include a high arched palate or cleft palate. Causes and Risks The specific causes of Pierre Robin syndrome are unknown; it can be part of many genetic syndromes. The lower jaw develops slowly over the first few months of fetal life but catches up over the first year after birth. Posterior placement of the tongue may cause choking episodes, feeding difficulty and
Disease - Pierre Robin Syndrome - Detroit, Michigan Disease pierre robin syndrome - courtesy of Henry Ford Health System of Detroit, Michigan. page Disease - pierre robin syndrome. http://www.henryfordhealth.org/12557.cfm
Extractions: Back to main Health Information page Infant hard and soft palates Definition: Pierre Robin syndrome (also called Pierre Robin complex or sequence) is a condition present at birth that is characterized by a very small lower jaw (micrognathia). The tongue tends to fall back and downward (glossoptosis) and there is cleft soft palate. Alternative Names: Robin sequence Causes And Risk: The specific causes of Pierre Robin syndrome are unknown. It can be part of many genetic syndromes. The lower jaw develops slowly over the first few months of fetal life but catches up over the first year after birth. Posterior placement of the tongue may cause choking episodes, feeding difficulty and breathing difficulties, especially while asleep. Prevention: Prevention of the syndrome is unknown. Treatment may reduce the number of episodes of breathing problems and choking. Symptoms: Signs And Tests: A physical examination is usually sufficient for your health care provider to diagnose this condition. A genetics consultation can rule out other associated anomalies and syndromes.
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Extractions: Pierre Robin Syndrome The condition is characterised by a small mandible (jaw bone), lack of tongue control with a high arched or cleft palate. Obstruction of the airway can occur due to the position of the tongue. Associated problems are feeding and breathing difficulties may be severe. However, the jaw continues to grow after birth and the condition improves with age. Inheritance Patterns : Most are sporadic events; some cases may be due to Stickler Syndrome which has autosomal dominant inheritance. Pre-Natal Diagnosis : Where a cleft palate is present it may be able to identify this using ultrasound scanning. Further information available from: Mrs Jacqui Mitchell,
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Extractions: Cleft Palate Foundation Publications Pierre Robin Sequence or Complex (pronounced "Roban") is the name given to a birth condition that involves the lower jaw being either small in size (micrognathia) or set back from the upper jaw (retrognathia). As a result, the tongue tends to be displaced back towards the throat, where it can fall back and obstruct the airway (glossoptosis). Most infants, but not all, will also have a cleft palate, but none will have a cleft lip Frequency estimates range from 1 in 2,000 to 30,000 births, based on how strictly the condition is defined. In contrast, cleft lip and/or palate occurs once in every 700 live births Parents who have had one child with isolated Robin Sequence probably have between a 1 and 5% chance of having another child with this condition. There have not yet been enough large-scale studies to make more accurate predictions ...
Disease - Pierre Robin Syndrome, North Carolina Disease pierre robin syndrome, Online Medical Encyclopedia courtesy of University Health Systems of Eastern Carolina serving 29 counties in eastern North http://www.uhseast.com/12049.cfm
Extractions: Back Email Us Search Centers of Excellence ... Disease Management Infant hard and soft palates Definition: Pierre Robin syndrome (also called Pierre Robin complex or sequence) is a condition present at birth that is characterized by a very small lower jaw (micrognathia). The tongue tends to fall back and downward (glossoptosis) and there is cleft soft palate. Alternative Names: Robin sequence Causes And Risk: The specific causes of Pierre Robin syndrome are unknown. It can be part of many genetic syndromes. The lower jaw develops slowly over the first few months of fetal life but catches up over the first year after birth. Posterior placement of the tongue may cause choking episodes, feeding difficulty and breathing difficulties, especially while asleep. Prevention: Prevention of the syndrome is unknown. Treatment may reduce the number of episodes of breathing problems and choking. Symptoms: Signs And Tests: A physical examination is usually sufficient for your health care provider to diagnose this condition. A genetics consultation can rule out other associated anomalies and syndromes.
Pierre Robin Syndrome pierre robin syndrome. Definition The specific causes of pierre robin syndrome are unknown; it can be part of many genetic syndromes. http://www.shands.org/health/information/article/001607.htm
Extractions: Causes, incidence, and risk factors: The specific causes of Pierre Robin syndrome are unknown; it can be part of many genetic syndromes. The lower jaw develops slowly over the first few months of fetal life but catches up over the first year after birth. Posterior placement of the tongue may cause choking episodes, feeding difficulty and breathing difficulties , especially while asleep. Treatment: Infants must be kept prone (face down), which allows gravity to pull the tongue forward and keep the airway open. These problems abate over the first few years as the lower jaw grows and assumes a more normal size. In moderate cases, the patient requires placement of a nasopharyngeal airway (a tube placed through the nose and into the airway) to avoid airway blockage. In severe cases, surgery is indicated for recurrent upper