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61. TheFetus.net - Pierre Robin Anomalad-Moshe Bronshtein MD
200207-08-11 pierre robin syndrome © Bronshtein www.TheFetus.net. Pierre Robin anomalad. Moshe Bronshtein MD. Department Obstetrics
http://www.thefetus.net/page.php?id=888

62. Alexa Web Search - Subjects > Health > Conditions And Diseases > Rare Disorders
pierre robin syndrome Subjects Health Conditions and Diseases Rare Disorders pierre robin syndrome. Sort by Most Popular.
http://www.alexa.com/browse/general?catid=523654&mode=general

63. 06/16/1997 - Association Between Toluene And Pierre Robin Syndrome.
Standard Interpretations 06/16/1997 Association between toluene and pierre robin syndrome.
http://www.osha.gov/pls/oshaweb/owadisp.show_document?p_table=INTERPRETATIONS&p_

64. PillSupplier.com - Conditions And Diseases/Rare Disorders/Pierre Robin Syndrome
Category pierre robin syndrome. HOME ABOUT US ORDER STATUS BMI CALCULATOR FAQ CONTACT US. Conditions and Diseases/Rare Disorders/pierre robin syndrome.
http://www.pillsupplier.com/dir/968/
Category: Pierre Robin Syndrome
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65. Jenny And Trevor's Story: SEDC And Complications At Birth - KSG Page
In Our Own Words A child with SED and Complications at Birth. Written by Jenny, a parent of Trevor with SED and pierre robin syndrome.
http://www.ksginfo.org/trev_prs.html
In Our Own Words:
A child with SED and Complications at Birth
Written by Jenny, a parent of Trevor with SED and Pierre Robin Syndrome . Trevor is now twelve years old. He had a vent until age three, trach tube until age eight.
I'll try to remember everything. Trevor was born full term by c-section, in the early 1990's. We did not know he was a dwarf, or that he had any medical problems until he was born.
He had severe respiratory problems, was intubated and put on a ventilator at birth, diagnosed with SED the next day. The docs tried to extubate, but it did not work. Bronchoscopy revealed severe tracheal, laryngeal and bronchial malasia and stenosis. He was trached at 5 days.
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.

66. Kniest And Spondyloepiphyseal And Spondylometaphyseal Dysplasia Page Medical Inf
Top of page. Links for pierre robin syndrome The Pierre Robin Network, a helpful site for new parents http//www.pierrerobin.org/;
http://www.ksginfo.org/info.html
Information about Kniest, SED, and SMD
Please click on the condition
you want to learn more about.

67. Pierre Robin Syndrome
Home Up . Click Here! pierre robin syndrome. Click Here! Musice.net Just-recipes.net EnvyMag.com Scholarships-4u.com Shesearch
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68. [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
Date Prev Date Next [Chronological] [Thread] ... [Top]
[DYSPHAGIA] Pediatric Pierre Robin Syndrome
http://www.new-vis.com

69. [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
Date Prev Date Next [Chronological] [Thread] ... [Top]
[DYSPHAGIA] Pediatric Pierre Robin Syndrome -Reply

70. Conditions And Diseases: Rare Disorders: Pierre Robin Syndrome| Treasure Coast H
Information on Conditions and Diseases, Rare Disorders, pierre robin syndrome and much more Treasure Coast Health. Treasure Coast
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71. OMIM - PIERRE ROBIN SYNDROME

http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=261800

72. OMIM - Online Mendelian Inheritance In Man
pierre robin syndrome. pierre robin syndrome AND OLIGODACTYLY. pierre robin syndrome WITH CONGENITAL HEART MALFORMATION AND CLUBFOOT.
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=PureSearch&db=omim&details_ter

73. Pierre Robin Syndrome
pierre robin syndrome Directory Guide to pierre robin syndrome sites on the internet. pierre robin syndrome.
http://www.directory.net/Health/Conditions_and_Diseases/Rare_Disorders/Pierre_Ro
Pierre Robin Syndrome Directory: Guide to Pierre Robin Syndrome sites on the internet. Search Engines: Google Yahoo MSN FindWhat ... City Guides
Pierre Robin Syndrome
Health Conditions and Diseases Rare Disorders Pierre Robin Syndrome Websites Pierre Robin Network http://www.pierrerobin.org
Provides general information about the condition, including genetics, issues and a glossary. Also offers an email group, message board, and personal accounts.
Contact a Family: Pierre Robin Syndrome
http://www.cafamily.org.uk/direct/p24.html
Main features of the condition and possible causes.
Chase's Story
http://www.pierrerobin.com
Personal account of one child's experience of this condition. Includes photographs.
NORD - Pierre Robin Syndrome
http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=pierre%20robin%20syndrome
Sample report, plus links to organisations. [Fee required for full report]
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74. Pierre Robin Syndrome From Linkspider UK Health Directory
pierre robin syndrome by Linkspider UK, pierre robin syndrome links and pierre robin syndrome topics from our Health directory.
http://linkspider.co.uk/Health/ConditionsandDiseases/RareDisorders/PierreRobinSy
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75. 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
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ajc store Gifts Photos/pages Browser tip  Make ajc.com  your homepage: ajc guides Schools Visitors Illustrated Health Encyclopedia Important notice 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

76. 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
Health Encyclopedia
Back to main Health Information page
Disease - Pierre Robin syndrome
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:
  • very small jaw with marked receding chin tongue appears large (is actually normal size but big relative to jaw) and is placed unusually far back in the oropharynx high arched palate cleft soft palate choking on tongue (a small opening in the roof of the mouth) natal teeth
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.

77. Medical Pierre Robin Syndrome
pierre robin syndrome. Mrs Jacqui Mitchell, pierre robin syndrome Contact group 83 Swallowfield road London SE7 7NT (Tel 0181 853 1811 evenings).
http://www.james.hopkins.easynet.co.uk/med_p1.html
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,
Pierre Robin Syndrome Contact group
83 Swallowfield road
London
(Tel: 0181 853 1811 evenings)
The Pierre robin contact group is a small Contact group. It offers:
  • Support especially for parents with new babies with the syndrome
  • Support and encouragement for parents with older children
Return to the Medical Index HOME EVENTS NEWS ... CONTACT US

78. Pierre Robin Syndrome
Tips for printing. pierre robin syndrome. Special Resources SOS Ask experts or consultants for information pierre robin syndrome.
http://ibis-birthdefects.org/start/piersyn.htm
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... Etchings Please Explore: 11 / 22 Translocation Stickler Syndrome Support Groups Professional Associations ... Key Information Sources Topics include Titles and Micrognathia Pierre Robin Syndrome Pierre Robin's sequence Retrognathia
Special Resources Pierre Robin Syndrome
A Selection of Internet Sites [*] Outstanding [P] For Professionals [S] Support Group [Dutch] [Norwegian] [Swedish] [Ukrainian] Pierre Robin syndrome [*][P] Pierre Robin Sequence [*][S] Information about Pierre Robin Sequence/Complex 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 ...

79. 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

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Disease - Pierre Robin syndrome
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:
  • very small jaw with marked receding chin tongue appears large (is actually normal size but big relative to jaw) and is placed unusually far back in the oropharynx high arched palate cleft soft palate choking on tongue (a small opening in the roof of the mouth) natal teeth
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.

80. 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
Disease Injury Nutrition Poison ... Infant hard and soft palates
Pierre Robin syndrome
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.
Alternative Names: Robin sequence
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.
Symptoms:
  • very small jaw with marked receding chin tongue appears large (is actually normal size but big relative to jaw) and is placed unusually far back in the oropharynx high arched palate cleft soft palate choking on tongue natal teeth

Signs and tests: Physical examination is usually sufficient for your health care provider to diagnose this condition.
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

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