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         Joubert Syndrome:     more detail
  1. Genodermatoses: Turner Syndrome, Joubert Syndrome, Neurofibromatosis, Von Hippel-lindau Disease, Tuberous Sclerosis, Freeman-Sheldon Syndrome
  2. Shannadoah: A Journey of Discovery About Dandy Walker, Joubert Syndrome, Helpful Resources and More by Shelley Boulet, 2003-04
  3. The Official Parent's Sourcebook on Joubert Syndrome: A Directory for the Internet Age by Icon Health Publications, 2005-01-30
  4. Joubert syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Kevin, MS, CGC Sweet, 2005
  5. Joubert syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Neurological Disorders</i> by Kevin, MS, CGC Sweet, Rosalyn, MD Carson-DeWitt, 2005
  6. Malformation Du Système Nerveux: Spina Bifida, Lissencéphalie, Malformations Congénitales Du Système Nerveux Central, Syndrome de Joubert (French Edition)
  7. Fibrocystic Diseases of the Liver (Clinical Gastroenterology)

41. Ocular Motor Apraxia: Joubert Syndrome
joubert syndrome. The results showed that her cerebellum, specifically her fourthventricle, exhibited a typical formation, characteristic of joubert syndrome.
http://wwweb.org/oma/messages/668.html
OMA Message Board message
Ref: http://wwweb.org/oma/messages/668.html Look at replies to this message Reply to this message Return to OMA Message Board Index Page ... Help file
joubert syndrome
From: T Jung, e-mail: tjung@tklp.com
Date: 05 Jun 2000 at 18:08
Replying to: message 645.html
I have a twenty-month-old daughter. She was diagnosed with OMA when she was a year old. We were then refereed to see a neuro optomologist who recommended a MRI. The results showed that her cerebellum, specifically her fourth ventricle, exhibited a typical formation, characteristic of Joubert syndrome. Typical behavioral characteristics associated with Joubert syndrome are poor balance, OMA, muscular hypotonia, slow speech development and behavioral problems. There is currently no genetic testing for Joubert. My daughter is doing fine and does not suffer from the above-described Joubert symptoms other than OMA. She started walking when she was 15 month old; however, her balance, although much improved, is at times tenuous. She is starting to utter sentences. Following is the link about Joubert Syndrome: http://www.ninds.nih.gov/patients/disorder/joubert/joubert.htm

42. Ocular Motor Apraxia: Re: Joubert Syndrome
Re joubert syndrome. From Lilians Canepa, email lilianscanepa@arnet.com.arDate 06 Sep 2002 at 0506 Replying to message 668.html
http://wwweb.org/oma/messages/1385.html
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Re: joubert syndrome
From: Lilians Canepa, e-mail: lilianscanepa@arnet.com.ar
Date: 06 Sep 2002 at 05:06
Replying to: message 668.html
Hola
Soy de la argentina y he estado explorando en busca de ayuda, quiero saber la posibilidad de algun lugar residencia o cualquier tipos de albergue que esté disponible para irnos con el bebé pues a él le detectaron sindrome joubert y antes queremos que el dr. chances le haga los estudios geneticos por lo que estamos realizando toda la documentacion correspondiente. Muchas gracias. Replies to this message: Reply to this message: The subject or title of the message that you would like to send (required):
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43. Joubert Syndrome : Meddie Health Search
ITEMS LINKS joubert syndrome Information sheet compiled by NINDS.(Rating 0.00 Votes 0) Rate It. joubert syndrome Foundation
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44. Joubert Syndrome
Subscribe now . joubert syndrome. joubert syndrome is a rare, genetic disorderthat affects the area of the brain that controls balance and coordination.
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Joubert Syndrome
Joubert syndrome is a rare, genetic disorder that affects the area of the brain that controls balance and coordination. The disorder is characterized by absence or underdevelopment of a part of the brain called the cerebellar vermis and a malformed brain stem. The most common features include ataxia (lack of muscle control), an abnormal breathing pattern called hypernea, sleep apnea, abnormal eye and tongue movements, and hypotonia. Other malformations such as extra fingers and toes, cleft lip or palate, tongue abnormalities, and seizures may also occur. There may be mild or moderate retardation. Treatment for Joubert syndrome is symptomatic and supportive. Infant stimulation and physical, occupational, and speech therapy may benefit some patients. Infants with abnormal breathing patterns should be monitored. The prognosis for individuals with Joubert syndrome varies. Some patients have a mild form with minimal motor disability and good mental development, while others may have severe motor disability and moderate mental retardation.

45. JOUBERT SYNDROME FOUNDATION 1025
joubert syndrome FOUNDATION 1025 6931 South Carlinda Avenue Columbia, MD 21046Tel (410) 9978084 Fax (410) 992-9184 E-Mail joubertduquette@home.com URL
http://www.faseb.org/genetics/ashg/ann-meet/2000-exlst/2000-ex-121a.htm

46. Joubert Syndrome
joubert syndrome. joubert syndrome is a rare, genetic disorder that affectsthe area of the brain that controls balance and coordination.
http://brandt.kurowski.net/projects/lsa/wiki/view.cgi?doc=961

47. WebMD -
Tap medicaltest-topic Jonston's Alopecia nord Joseph Disease shc Joseph'sDisease nord joubert syndrome joubert syndrome nord joubert syndrome
http://my.webmd.com/content/healthwise/152/37747.htm

48. Health Library - Joubert Syndrome
Your Health. Search. joubert syndrome. Self Help Clearinghouse. joubert syndromeFoundation. International network. 7 chapters. Founded 1992.
http://yourhealth.stlukesonline.org/Library/HealthGuide/SelfHelp/topic.asp?hwid=

49. Health Library - Joubert Syndrome
Your Health. Search. joubert syndrome. Cerebellarparenchymal Disorder IV; CerebelloparenchymalDisorder IV Familial; Chorireninal Colobomajoubert syndrome;
http://yourhealth.stlukesonline.org/Library/HealthGuide/IllnessConditions/topic.

50. Health Library - Joubert Syndrome
Advanced Search. joubert syndrome. Self Help Clearinghouse. JoubertSyndrome Foundation. International network. 7 chapters.
http://www.stjudemedicalcenter.org/Library/HealthGuide/SelfHelp/topic.asp?hwid=s

51. Health Library - Joubert Syndrome
Advanced Search. joubert syndrome. Cerebellarparenchymal Disorder IV; CerebelloparenchymalDisorder IV Familial; Chorireninal Colobomajoubert syndrome;
http://www.stjudemedicalcenter.org/library/healthguide/IllnessConditions/topic.a

52. 1Up Health > Joubert Syndrome - Birth Defects & Genetic Disorders
joubert syndrome . Read detailed information about joubert syndrome . 1Up Health Diseases Conditions Birth Defects Genetics joubert syndrome.
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53. 1Up Health > Health Links Directory > Conditions And Diseases: Genetic Disorders
Conditions and Diseases Genetic Disorders joubert syndrome . Uncover Sites.joubert syndrome Information sheet compiled by NINDS. Joubert
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... Genetic Disorders : Joubert Syndrome Description
Sites Joubert Syndrome
Information sheet compiled by NINDS.
Joubert Syndrome Foundation
Organization, conferences and contact details. FAQs about the disease, information center and resources. National Library of Medicine: Joubert syndrome Synonyms, a summary and a list of major features for this disorder. Readers Digest Health A brief discussion about joubert syndrome, its alternate names and further resources. TheFetus.net A detailed look at joubert syndrome starting with a definition, etiology, prenatal diagnosis, clinical findings, genetics and prognosis. Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor Parts of the directory made available on 1UpHealth have been modified. External Web site links provided on this site are meant for convenience and for informational purposes only; they do not constitute an endorsement. Search: The information provided herein should not be used during any medical emergency or for the diagnosis or treatment of any medical condition. A licensed physician should be consulted for diagnosis and treatment of any and all medical conditions. Call 911 for all medical emergencies. Links to other sites are provided for information only they do not constitute endorsements of those other sites.

54. Searchalot Directory For Joubert Syndrome
Related Web Sites. joubert syndrome Foundation Organization, conferences andcontact details. joubert syndrome - Information sheet compiled by NINDS.
http://www.searchalot.com/Top/Health/ConditionsandDiseases/GeneticDisorders/Joub
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55. Syndroom Van Joubert
Vermis Aplasia Cerebellarparenchymal Disorder IV Cerebelloparenchymal Disorder IVFamilial Chorireninal Colobomajoubert syndrome Hyperpnea Episodic-Abnormal
http://www.erfocentrum.nl/zena/joube.php
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... Ziekten en aandoeningen Syndroom van Joubert
Syndroom van Joubert Synoniemen
Cerebellar Vermis Agenesis
Hypernea
Episodic-Eye Moves-Ataxia-Retardation
Cerebellar Vermis Aplasia
Cerebellarparenchymal Disorder IV
Cerebelloparenchymal Disorder IV Familial
Chorireninal Coloboma-Joubert Syndrome Hyperpnea
Episodic-Abnormal Eye Movement
Joubert-Bolthauser Syndrome Kidneys Cystic-Retinal Aplasia Joubert Syndrome Polydactyly-Joubert Syndrome Retinal Aplastic-Cystic Kidneys-Joubert Syndrome Vermis Aplasia Vermis Cerebellar Agenesis Korte beschrijving Het syndroom is een bijzonder zeldzame neurologische aandoening. De hersenstructuur is onvoldoende ontwikkeld, wat een verminderde spierspanning, ontwikkelingsachterstand, abnormale ademhaling en abnormale oogbeweging als gevolg heeft. Diagnose De diagnose kan worden gesteld door intensief neurologisch onderzoek. Behandeling Er is geen behandeling bekend voor het syndroom van Joubert. Voorkomen Extreem zeldzaam.

56. Joubert Syndrome Support Group
joubert syndrome Support Group 76/78 Coniston Avenue Little Hulton WorsleyManchester M38 9WZ Tel 0161 9500749 Helpline 0161 7992502
http://www.dialdoncaster.co.uk/supgrops/natgroup/nat179.htm
Home Support Organisations Fact Sheets Information Sheets ... Help using this site
Joubert Syndrome Support Group 76/78 Coniston Avenue
Little Hulton
Worsley
Manchester
Tel:
Helpline:
Description:
Works to promote awareness of Joubert Syndrome.
Provides support for families effected by Jourbert Syndrome.
Whilst all the information given in this document was correct at the time of going to press, DiAL Doncaster cannot be held responsible for any subsequent changes. Return to National Support Organisations starting with J

57. Joubert Syndrome
joubert syndrome PubMed Medline search on joubert syndrome joubert syndrome factsheetNational Institute for Neurological Disorders and Stroke. Support Groups.
http://www.ion.ucl.ac.uk/library/patient/joubert.htm
Joubert syndrome PubMed Medline search on Joubert Syndrome
Joubert Syndrome
factsheet: National Institute for Neurological Disorders and Stroke Support Groups Joubert Syndrome Foundation

12348 Summer Meadow Rd. Rock, MI, 49880, USA
Tel: 906-359-4707
Email: joubertfoundation@joubertfoundation.com
This is an international network of parents who share knowledge, experience, and emotional support. The group offers a networking list, newsletter, and a biannual conference. The US based website has an information centre and FAQ's.

58. Mioti: Medical Condition
not available. NINDS joubert syndrome Information Page....... Condition joubert syndrome. Neuromuscular joubert syndrome.
http://www.mioti.com/cat/condition/condition.asp?Cat=JoubertSyndrome

59. Service Page - Pathologie Information
joubert syndrome is an autosomalrecessive disorder characterized by cerebellar hypoplasia,hypotonia, developmental delay, abnormal respiratory patterns, and
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=475

60. Health Library - Joubert Syndrome
SEARCH. joubert syndrome. Self Help Clearinghouse. joubert syndrome Foundation.International network. 7 chapters. Founded 1992.
http://www.muskogeehealth.com/Library/HealthGuide/SelfHelp/topic.asp?hwid=shc29j

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