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All Topic Areas 1 - 10 of 916  more >> Syndrome X Scheie syndrome Asperger's Syndrome Down Syndrome Trisomy 21 47,XX,+21 47,XY,+21 Marfan Syndrome Arachnodactyly MFS Articles 1 - 5 of 157  more >> Landau-Kleffner Syndrome Information Page Landau-Kleffner syndrome (LKS) is a rare, childhood neurological disorder characterized by the sudden or gradual development of aphasia (the inability to understand or express language) and an abnormal electro-encephalogram (EEG). LKS affects the parts of the brain that control comprehension and speech. The disorder usually occurs in children between the ages of 5 and 7 years. Typically, children with LKS develop normally but then lose their language skills for no apparent reason. While many of... National Institute of Neurological Disorders and Stroke Aicardi Syndrome Information Page Aicardi Syndrome is a rare genetic disorder characterized by the partial or complete absence of the structure that links the two hemispheres of the brain, the corpus callosum. The disorder affects only girls. Onset of Aicardi Syndrome generally begins between the ages of 3 and 5 months with infantile spasms, a type of childhood seizure. Symptoms include seizures, mental retardation and lesions on the retina of the eye that are specific to the disorder. Aicardi Syndrome may be associated with... National Institute of Neurological Disorders and Stroke Angelman Syndrome Information Page Angelman syndrome is a chromosomal (gene-linked) disease that causes neurological problems. The physician Harold Angelman first identified the syndrome in 1965, when he described several children in his practice as having "flat heads, jerky movements, protruding tongues, and bouts of laughter." Infants with Angelman syndrome appear normal at birth, but begin to have feeding problems at 1-2 months and noticeable developmental delays by 6 to 12 months. Seizures may often begin before the age of 3... National Institute of Neurological Disorders and Stroke Asperger Syndrome Information Page Asperger syndrome (AS) is a developmental disorder.  It is an autism spectrum disorder (ASD), one of a distinct group of neurological conditions characterized by a greater or lesser degree of impairment in language and communication skills, as well as repetitive or restrictive patterns of thought and behavior.  Other ASDs include:  classic autism, Rett syndrome, childhood disintegrative disorder, and pervasive developmental disorder not otherwise specified (usually referred to as... National Institute of Neurological Disorders and Stroke Barth Syndrome Information Page Barth syndrome is a rare congenital metabolic and neuromuscular disorder that affects boys. It is passed from mother to son through the sex-linked, or X, chromosome. Symptoms affect multiple systems of the body and may include changes to metabolism, motor delays, hypotonia (reduced muscle tone), delayed growth, cardiomyopathy (leading to a poorly functioning heart), weakened immune system, chronic fatigue, lack of stamina, hypoglycemia (low blood sugar), mouth ulcers, diarrhea, and varying... National Institute of Neurological Disorders and Stroke Organizations 1 - 5 of 35  more >> Angelman Syndrome Foundation - http://www.asclepius.com/angel/ Lowe Syndrome Association, Inc. - http://www.lowesyndrome.org/ National Association for Down Syndrome - http://www.nads.org/ National Down Syndrome Congress - http://www.ndsccenter.org/ National Down Syndrome Society - http://www.ndss.org/ News 1 - 5 of 887  more >> Down Syndrome Brain Function Improved In Mice MedicalNewsToday - Mon, 26 Feb 2007 08:00 EST Human Factors/ergonomics Research Can Help Workers Avoid Carpal Tunnel Syndrome MedicalNewsToday - Fri, 02 Mar 2007 02:00 EST Pharmacist-Driven Outreach Lowers Metabolic Syndrome Rates MedicalNewsToday - Sun, 04 Mar 2007 10:00 EST Pharmacist-driven Outreach Lowers Metabolic Syndrome Rates ScienceDaily - Wed, 28 Feb 2007 04:00 EST Drug may treat mental symptoms of Down syndrome Reuters - Sun, 25 Feb 2007 06:13 EST Clinical Trials 1 - 5 of 1776  more >> Jugular Vein Sampling for Hormone Levels for the Diagnosis of Cushing Syndrome ClinicalTrials.gov Identifier: NCT00001453 - Active, not recruiting Cushing's Syndrome Study of Hypercortisolism in Cushing's Syndrome and Stress-Induced Pseudo-Cushing's Syndrome ClinicalTrials.gov Identifier: NCT00004343 - Active, not recruiting Cushing's Syndrome IGF-I/IGFBP-3 Therapy in Children and Adolescents With Growth Hormone Insenitivity Syndrome (GHIS) Such as Laron Syndrome ClinicalTrials.gov Identifier: NCT00368173 - Active, not recruiting Growth Hormone Insensitivity Syndrome (GHIS); Laron Syndrome Amifostine in Treating Patients With Myelodysplastic Syndrome ClinicalTrials.gov Identifier: NCT00003048 - Active, not recruiting Previously Treated Myelodysplastic Syndrome; secondary myelodysplastic syndrome; de novo myelodysplastic syndrome Study of Genetic and Molecular Defects in Primary Immunodeficiency Disorders ClinicalTrials.gov Identifier: NCT00004341 - Active, not recruiting X-linked agammaglobulinemia; X-linked hyper IgM syndrome; Wiskott-Aldrich Syndrome; Leukocyte Adhesion Deficiency Syndrome

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