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Syndrome - Articles Tagged Syndrome On Encyclocentral.com |
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Rett Syndrome Neuro Developmental Disorder Genetic Defect
Rett syndrome is a neuro developmental disorder. It is categorized as a pervasive developmental disorder by the DSM-IV. Many scientists consider this as a wrong categorization like such disorders as fragile X syndrome, tuberous sclerosis, or Down syndrome. All the above disorders display a kind of autistic features. The symptoms of this disorder are similar to those of Angelman syndrome and autism.
Posted on March 26, 2008 | Related Articles | Linked From
(296 Reads) tag Health Tags: autism, chromosome, defect, developmental, disorder, females, genetic, mecp, neuro, rett, symptoms, syndrome, Infant Small Feet Developmental Disorder, Developmental Of Genetic Defects, Wringing With Sensory Defect, What Is The Genetic Defect In Rett Syndrome, Videos Of Early Signs Of Rett Syndrome, Lazy Eye Syndrome Genetic Disorder
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Crigler Najjar Syndrome Infant Jaundice And Brain Damage
Crigler-Najjar syndrome is a rare hereditary disorder in infants. It is a defect of bilirubin metabolism that leads to non-haemolytic jaundice, ultimately resulting in brain damage. The syndrome exists in two forms- types I and II. The type II syndrome is also known as Arias syndrome. While inheritance in type I is autonomic recessive, in type II it plays a dominant role.
Posted on February 04, 2008 | Related Articles | Linked From
(268 Reads) tag Health Tags: bilirubin, brain, crigler, damage, disorder, infant, jaundice, najjar, syndrome, therapy, type, Brain Damage Infant Jaundice, Jaundice Brain Injury Diabetes, Rett Syndrome Pictures Of Infant, Nicole Kidman Baby Fragile X, Brain Damages Or Malfunctions During Early Childhood
Smith Lemli Opitz Syndrome Metabolism Disorder
Smith Lemli Opitz Syndrome is a disorder affecting the all round development and metabolism of a body. It is also known as 7-dehydrocholesterol reductase deficiency. It may result in a number of problems such as mental retardation, deformed facial features, learning difficulties and behavioral irregularities. Affecting approximately 1 in 20,000 to 40,000 the disorder is most common among Caucasians of European ancestry.
Posted on February 03, 2008 | Related Articles | Linked From
(229 Reads) tag Health Tags: cholesterol, dhcr, disorder, enzyme, lemli, metabolism, opitz, patients, production, slos, smith, syndrome, Smith Lemli Opitz Syndrome Estrada, Smith Lemli Opitz Kousseff, Smith Lemli Opitz Disorder, Scoring For Smith Lemli Opitz Syndrome, How To Diagnose Smith Lemli Opitz Syndrome, Pictures Of Smith Lemli Opitz Disorder, Life Expectancy In Opitz Syndrome, Habba Syndrome And Pancreas
Turner Syndrome Chromosomal Conditions
Turner syndrome consists of several chromosomal conditions that refer to complications in females. People with this syndrome have female characteristics but are generally underdeveloped and consist of females with a different chromosomal configuration.
Posted on December 25, 2007 | Related Articles | Linked From
(662 Reads) tag Health Tags: chromosomal, conditions, female, females, syndrome, turner, Pictures Of Turner Syndrome, Turner's Syndrome Pictures, Pictures Of Women With Turner Syndrome, What Genetic Treatments Are There For People Suffering From Turner Syndrome, Pictures Women With Turner Syndrome, Chromosomal Configuration In Females
Rhett Syndrome Neurodevelopmental Symptoms Hypotonia And Apraxia
Rhett Syndrome is a childhood disorder of the nervous development. A normal early development is usually followed by the loss of normal use of hand, distinctive hand movements, slow growth of head as well as the brain, abnormalities in the gait and ultimately mental retardation. The occurrence is almost entirely noticed in the females.
Posted on December 24, 2007 | Related Articles | Linked From
(1588 Reads) tag Health Tags: apraxia, child, disorder, genes, hypotonia, neurodevelopmental, normal, rhett, symptoms, syndrome, What Is Rhett Syndrome, What Is Rhetts Disorder, Hypotonia More Condition Symptoms, What Are The Symptoms Of Rhetts, Syndromes With Symptom Of Hypotonia, Early Signs Of Rhett Syndrome, Is Apraxia Related To Autism, Childhood Apraxia Is It Curable, Apraxia Brain Cancer Lung, Syndrome Small Feet Hypotonia
Habba Syndrome Gall Bladder Malady
Habba syndrome is a disease characterized by chronic diarrhea, caused due to a dysfunctional but intact gall bladder. This malady gets name from its discoverer Dr. Saad. F. Habba. Dr. Habba, M.D. is a graduate from the Royal College of Surgeons, Ireland is a practicing gastroenterologist for the last 30 years. He was Chief of Gasterointestinal Endoscopy at the University of Medicine and Dentistry of New Jersey and is currently in private practice in Summit New Jersey.
Posted on August 17, 2007 | Related Articles | Linked From
(5910 Reads) tag Health Tags: bile, bladder, diarrhea, gall, habba, malady, response, syndrome, Www Dateline Msnbc Com, Disida Scan With Cck Injection, Tp Www Google Com Pr, Dr Saad F Habba, Dr Habba New Jersey, Rett Syndrome Gallbladder Disorders, Gallbladder Malfunction And Diarrhea, Skin Malady On Bladder, Habba Syndrome And Lyme Disease
Downs Syndrome Recent Research Shows Increase In Number Of Afflicted Children
Eddie, a five year old son of Simon Barnes who is a Times journalist, has been suffering from Down's syndrome. It has been reported that more and more babies are born with this very disease. In the year 1989 a widespread screening was started that had lead to the fall of the new instances of Down’s syndrome.
Posted on November 24, 2008 | Related Articles | Linked From
(23 Reads) tag Health Tags: afflicted, child, children, disease, downs, increase, recent, research, shows, syndrome, Downs Syndrome Increase Numbers
Pretzel Syndrome Gene Disorder
William is an eight year old child. But he is different from other children in that he has a disproportionate head setting on his shoulders. He does not have friends because he is mentally not as active as them and he does not go to school because of his poor health conditions. He has a very abnormal posture, gets seizures frequently and his mother cannot take him out with her as he urinates frequently. He also has visionary problems. When he was taken to a hospital he was diagnosed as suffering from a disease called pretzel syndrome, a single gene disorder of the LYK5 gene.
Posted on October 30, 2007 | Related Articles | Linked From
(482 Reads) tag Health Tags: condition, disorder, gene, pretzel, syndrome, Lyk 5 Pretzel Syndrome, Wiki Weak Eye Muscles, What Is The Pretzel In Psychiatry, Skin Tags Infant Syndromes Low Tone Photos, Pretzels Causing Breathing Difficulties
All Syndrome Articles (31 stories on 4 pages)
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