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Topic: Marden Walker syndrome


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In the News (Wed 30 Dec 09)

  
  Marden Walker Syndrome
Marden-Walker Syndrome is a rare connective tissue disorder that is inherited as an autosomal recessive trait.
Cerebro-Oculo-Facio-Skeletal Syndrome is a genetic degenerative disorder of the brain and spinal chord that is present at birth.
Cerebro-Oculo-Facio-Skeletal Syndrome is inherited as an autosomal recessive trait.
hw.healthdialog.com /kbase/nord/nord895.htm   (987 words)

  
 Marden-Walker syndrome   (Site not responding. Last check: 2007-11-01)
Marden and Walker described in 1966 a female infant with blepharophimosis, joint contractures, arachnodactyly and growth and developmental delay, who died of pneumonia at 3 months.
MWS signs are mostly present in the neonatal period and the most frequent manifestations include multiple congenital joint contractures, dysmorphic features with a mask-like face, blepharophimosis, ptosis, micrognathia, cleft or high-arched palate, low-set ears, arachnodactyly, decreased muscular mass.
Initially described as a syndrome, this condition is more likely to be the phenotypic expression of various heterogeneous diseases and belongs to group II in the classification of arthrogryposis.
www.orpha.net /static/GB/mardenwalker_syndrome.html   (2320 words)

  
  Schwartz-Jampel syndrome: Encyclopedia of Genetic Disorders
Schwartz-Jampel syndrome (SJS) is a rare, inherited condition of the skeletal and muscle systems that causes short stature, joint limitations, and particular facial features.
First described in 1962, SJS is now a clearly defined syndrome that is divided into two types.
SJS is a very rare genetic syndrome that affects males and females in many ethnic backgrounds.
health.enotes.com /genetic-disorders-encyclopedia/schwartz-jampel-syndrome   (2091 words)

  
 :: Medical Information ::
It is possible that the main title of the report Marden Walker Syndrome is not the name you expected.
Marden-Walker syndrome is a rare connective tissue disorder that is inherited as an autosomal recessive trait.
Patients with this disorder typically have a distinct facial expression, a cleft or high-arched palate, small or receding jaw (micrognathia), bone joints in a fixed position, growth delay and limited control of muscle movement.
www.medical-health-care-information.com /encyclopedia/m/Marden-Walker-Syndrome.asp   (582 words)

  
 Avenues: A National Support Group for Arthrogryposis Multiplex Congenita | Medline Abstracts, Arthrogryposis, 1997-1998
Four children (18.2%) were found to suffer from functional complications (mild dumping syndrome, retrosternal pain, vomiting during episodes of asthma, dysphagia).
No gas bloat syndrome occurred within the follow-up interval and all children were able to belch and vomit.
Clasped thumb can be seen in conjunction with syndromes such as arthrogryposis and, in these cases, recognition of the abnormal anatomic structures is required to effect satisfactory reconstruction.
www.avenuesforamc.com /research/biblio.htm   (4739 words)

  
 Rare Pediatric Disease Database   (Site not responding. Last check: 2007-11-01)
Head and Neck: MWS is often associated with characteristic facial features such as small eyes, eyes that are wider apart then usual, a small mouth and jaw, a hole in the roof of the mouth (cleft palate) or a high roof of the mouth (high arched palate), and abnormally shaped ears.
In autosomal recessive diseases, when a person has two abnormal genes, he or she is affected with the disease; in this case, Marden-Walker syndrome.
It may vary from individual to individual depending on which areas of the body are affected and the severity of the defects.
www.madisonsfoundation.org /content/3/1/display.asp?did=487   (717 words)

  
 Indian Pediatrics - Editorial
Marden Walker Syndrome is an autosomal recessive disorder characterized by failure to thrive, marked motor and mental retardation, multiple malformations in the form of peculiar facies associated with small muscle mass, kyphoscoliosis and arachnodactyly.
Dandy Walker cyst and pulmonary hypoplasia have also been reported.
Schwartz-Jample syndrome sometimes simulates this condition, but is differentiated by generalized hypertrophy of muscles and continuous electrical activity in EMG.
www.indianpediatrics.net /sep2002/sep-878.htm   (183 words)

  
 Medical Dictionary: Marden Walker like syndrome - WrongDiagnosis.com
Marden Walker like syndrome is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH).
This means that Marden Walker like syndrome, or a subtype of Marden Walker like syndrome, affects less than 200,000 people in the US population.
They list Marden Walker like syndrome as a "rare disease".
www.wrongdiagnosis.com /medical/marden_walker_like_syndrome.htm   (294 words)

  
 Shannadoah.com   (Site not responding. Last check: 2007-11-01)
Dandy Walker is diagnosed with a presence of some or all of a variety of features.
Dandy Walker is described as Dandy Walker Variant, Dandy Walker Syndrome, Dandy Walker Malformation, and Dandy Walker Complex.
With Dandy Walker the cerebellum is not developed properly.
www.shannadoah.com /dandywalker.html   (450 words)

  
 Developmental and genetic diseases
Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness (Thiamine-responsive megaloblastic anemia syndrome [1])
Membranous obstruction of the inferior vena cava (Budd-Chiari syndrome [41])
Myotonic myopathy, dwarfism, chondrodystrophy, and ocular and facial abnormalities (Schwartz-Jampel syndrome [5])
www.gfmer.ch /genetic_diseases_v2/index.php?disinit=M   (1104 words)

  
 [No title]   (Site not responding. Last check: 2007-11-01)
He may be only 7 months old, but already Dakota Mankus has met with enough adversity to last a lifetime.
Born with a rare genetic condition, Marden Walker syndrome, Dakota is one of only 30 people diagnosed worldwide.
He was diagnosed with Marden Walker syndrome at 3 weeks.
www.rivertowns.net /news1999/hsorival/week41/frontpage/np/SPORB01.HTM   (478 words)

  
 Marden Walker Syndrome
It is possible that the main title of the report Marden Walker Syndrome is not the name you expected.
Patients with this disorder typically have a distinct facial expression, a cleft or high-arched palate, small or receding jaw (micrognathia), bone joints in a fixed position, growth delay and limited control of muscle movement.
Marden-Walker syndrome affects males more often than females.
www.seton.net /health_a_to_z/health_library/support_group/marden_walker_syndrome   (396 words)

  
 Marden Walker Like Syndrome
syndrome see Jaw-winking syndrome Marden-Walker syndrome Marfan like habitus see Marfanoid habitus Marfanoid habitus Marfan's syndrome...
Definition of Marden Walker like syndrome in an online ecyclopedia or dictionary.
We hope that this diseases directory has been of use in finding information regarding our illness or disease.
www.medicality.org.uk /diseases/marden-walker-like-syndrome.php   (137 words)

  
 Marden-Walker Syndrome - [Support Group] - Quest Diagnostics Patient Health Library
Marden-Walker Syndrome - [Support Group] - Quest Diagnostics Patient Health Library
This information is provided as a resource and does not constitute an endorsement for any group.
Healthwise disclaims any liability for the decisions you make based on this information.
www.questdiagnostics.com /kbase/shc/shc29maw.htm   (201 words)

  
 Marden Walker Syndrome - SJMMC, Ann Arbor, Michigan MI
Marden Walker Syndrome - SJMMC, Ann Arbor, Michigan MI Online Health Information
Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report.
To search for documents containing all of your keywords simply enter the words.
www.sjmercyhealth.org /14479.cfm   (390 words)

  
 Marden-walker Syndrome
Popular Searches: The National Marden Walker Syndrome Discussion Forum.
Welcome to the National Marden Walker Syndrome Discussion Forum.
Arch Pediatr Adolesc Med -- Abstract: Zollinger-Ellison syndrome...
www.medicality.org.uk /diseases/marden-walker-syndrome.php   (104 words)

  
 canine cushings syndrome
… Introduction: Often called simply "Cushing's Syndrome", hyperadrenocorticism describes the clinical signs referable to the excessive levels of serum …
Cushing’s syndrome is a condition in which there is an excess of cortisol (cortisone).
Canine Cushings syndrome or Hyperadrenocorticism Canine Cushing's syndrome or hyperadrenocorticism is caused by the production of too much adrenal hormone, in …
www.touchofclasscomfortinn.com /canine-cushings-syndrome.html   (205 words)

  
 Marden-Walker Syndrome - SJMMC, Ann Arbor, Michigan MI
This information is provided as a resource and does not constitute an endorsement for any group.
For evidence-based information on diseases, conditions, symptoms, treatment and wellness issues, continue searching this site.
Mutual support and education for families affected by Marden-Walker syndrome.
www.sjmercyhealth.org /14480.cfm   (225 words)

  
 The Marden-Walker syndrome -- King and Magenis 15 (5): 366 -- Journal of Medical Genetics
The Marden-Walker syndrome -- King and Magenis 15 (5): 366 -- Journal of Medical Genetics
growth and developmental delay of the Marden-Walker syndrome were present
Copyright © 1978 by the BMJ Publishing Group Ltd.
jmg.bmjjournals.com /cgi/content/abstract/15/5/366   (104 words)

  
 Genetic Health Services Victoria Useful Links
Foetal Alcohol Syndrome: National Organization on Fetal Alcohol Syndrome
Nager syndrome: Foundation for Nager and Miller Syndromes
Von Hippel-Lindau Syndrome : VHL Family Alliance and VHL Syndrome
www.genetichealthvic.net.au /pages/links.html   (129 words)

  
 Health Library
Mycosis fungoides and the sezary syndrome: Treatment - Health Professional Information [NCI PDQ]
Mycosis fungoides and the sezary syndrome: Treatment - Patient Information [NCI PDQ]
Myelodysplastic syndromes: Treatment - Health Professional Information [NCI PDQ]
www.wellspan.org /library/healthguide/en-us/IllnessConditions/SearchResults.asp?letter=M&module_name=Illnesses   (359 words)

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