Extractions: The names were derived from the specific illness/disease source directories. Therefore, there are some variations in the names. When ordering a list of URLs for your illness/disease, where possible, include the general usage, technical, acronym, and/or abbreviation names. C Syndrome C.F.S. CABG or "Cabbage" (Coronary Artery Bypass Graft Surgery) Cachexia CAD Cadmium Poisoning Caesarean Section Cafe-au-Lait Spots Caffeine Addiction Caffeine Intoxication Caisson Disease Calcaneus Calciferol Calcific Bursitis Calcific Tendonitis Calcification Calcitonin-Osteoporosis Calcium Channel Blockers Calcium Metabolism Disorders Calcium Pyrophosphate Deposition Disease (Pseudogout) Calculi Calculi, Biliary Calculus Calculus, Dental Caldwell-Luc Operation Caliper Callus Camptomelic Syndrome Campylobacter Campylobacter Enteritis Campylobacter Infection Campylobacteriosis Canaliculus Canalis Canavan Disease Cancer Cancer - New therapies in the pipeline Cancer (Reproductive Tract) Cancer and Aging Cancer antigen 125 (CA 125) for functional ovarian cysts Cancer Care Cancer Causes Cancer Center Cancer Concerns, Men
Extractions: Home About Links Index ... Editor's Choice Paid Advertisement (click above). Please see the privacy statement Endocrinology Growth Assorted Pages Delayed Growth Calculation of Growth Delay Growth Delay Onset Determination Achondroplasia ... Risser Sign Familial Short Stature Book Home Page Cardiovascular Medicine Dental Dermatology Emergency Medicine Endocrinology Gastroenterology General Medicine Geriatric Medicine Gynecology Hematology and Oncology HIV Infectious Disease Jokes Laboratory Neonatology Nephrology Neurology Obstetrics Ophthalmology Orthopedics Otolaryngology Pediatrics Pharmacology Prevention Psychiatry Pulmonology Radiology Rheumatology Sports Medicine Surgery Urology Chapter Endocrinology Index Adrenal Disease General Cardiovascular Medicine Diabetes Mellitus Examination Ophthalmology Geriatric Medicine Growth Hematology and Oncology Hypoglycemia Laboratory Metabolism Neonatology Obesity Obstetrics Parathyroid Disease Pediatrics Pharmacology Pituitary Disease Prevention Radiology Nephrology Sex Sports Medicine Surgery Symptom Evaluation Thyroid Disease Page Growth Index Short Short Calculation Short Onset Short Achondroplasia Short Constitutional Short Familial Tall Tall Cerebral Gigantism Signs Short parents Normal birth history and gestational weight Short stature Normal Linear Growth Velocity for age Bone age consistent with chronological age Normal age for the onset of Puberty Absence of organic or psychologic disease Search other websites for this topic Search National Library of Medicine PubMed for related articles Search Google for related
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Extractions: MSActiveSource - Click Here Information on Human Neurological Diseases Web sites providing information on human neurological diseases can be accessed via this section. Table of Contents of This Section Acid Maltase Deficiency Acquired Epileptiform Aphasia Acute Disseminated Encephalomyelitis ADHD Adrenoleukodystrophy Affective Disorders (Depression, Manic-Depression) Agenesis of the Corpus Callosum Agnosia Aicardi Syndrome AIDS - Neurological Manifestations Alcoholism Alexander Disease Alpers' Disease Alternating Hemiplegia of Childhood Alzheimer's Disease Amyotrophic Lateral Sclerosis (ALS) Anencephaly Aneurysm Angelman Syndrome Angiomatosis Anosmia Anoxia or Hypoxia Anxiety and Panic Disorders Aphasia Apraxia Arachnoid Cysts Arachnoiditis Arnold-Chiari Malformation Arteriovenous Malformation Asperger Syndrome Ataxia Atrophy Attention Deficit Disorder Autism Autonomic Disorders Back Pain and Disk Disease Batten Disease Behcet's Disease Bell's Palsy Benign Essential Blepharospasm Benign Focal Amyotrophy Benign Intracranial Hypertension Binswanger's Disease Blepharospasm Blindness Botulism Brachial Plexus Birth Injuries Brachial Plexus Injuries Brain Aneurysm Brain Injury Brain Tumors Brown-Sequard Syndrome Canavan Disease Carpal Tunnel Syndrome Causalgia Central Pain Syndrome Cephalic Disorders Cerebral Aneurysm Cerebral Arteriosclerosis Cerebral Atrophy Cerebral Gigantism Cerebral Palsy Cervical Dystonia Charcot-Marie-Tooth Disease Chiari Malformations Chorea Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)
GASNet Anesthesiology: Contents S - Z Smith. Smith Lemli - Opitz Syndrome. Sotos. Sotos's Syndrome (CerebralGigantism). Spatz. Hallervorden - Spatz Disease. Stevens. Erythema http://gasnet.med.yale.edu/pediatric-syndromes/s2z_br.php
Extractions: Contents S - Z - pediatric syndromes - Sachs Tay - Sachs Disease Saethre Saetre - Chotzen Syndrome Sanfilippo Sanfilippo Syndrome (Mucopolysaccharidosis Type III) Scheie Scheie Disease (Mucopolysaccharidosis Type V) Schönberg Albers - Schönberg Disease (Osteopetrosis, Marble Bone Disease) Schönlein Henoch - Schönlein Purpura Schuller Hand - Schuller - Christian Disease (Histiocytosis X) Schwartz Schwartz - Jampel Syndrome Scleroderma Scleroderma Senior Senior - Loken Syndrome Seip Seip - Lawrence Syndrome Sheldon Freeman - Sheldon Syndrome (Whistling Face Syndrome) Shone Shone Syndrome Shy Shy - Drager Syndrome Siemens Christ - Siemens - Touraine Syndrome (Anhydrotic Ectodermal Dysplasia) Silver Russell - Silver Syndrome Sipple Sipple's Syndrome (MEN - type II) Siwe Letterer - Siwe Disease (Acute Disseminated Histiocytosis) Smith Smith - Lemli - Opitz Syndrome Sotos Sotos's Syndrome (Cerebral Gigantism) Spatz Hallervorden - Spatz Disease Stevens Erythema Multiforme Major (Stevens - Johnson Syndrome) Steinert Myotonic Dystrophy (Steinert's Disease) Stickler Stickler Syndrome Still Still's Disease Strandberg Groenblad - Strandberg Syndrome (Pseudoxanthoma Elasticum) Streiff Hallerman - Streiff Syndrome Sturge Sturge - Weber Syndrome Sulzberger Bloch - Sulzberger Syndrome Sydenham Sydenham's Chorea System Lupus Erythematous System Lupus Erythematous Tangier Tangier Disease (Analphalipoproteinemia) TAR TAR Syndrome (Thrombocytopenia and Absent Radius) Tauri Tauri Disease (Glygogen Storage Disease Type VII) Tay Tay - Sachs Disease Taybi Rubenstein - Taybi Syndrome Telangiectasia
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Sotosin Oireyhtymä Kehitysvammahuollon tietopankki. Sotosin oireyhtymä. Serebraaligigantismi. Sotosinoireyhtymä on ilmeisesti sangen monimutkaisesti perinnöllinen sairaus. http://www.saunalahti.fi/kup/syndroma/sotos.htm
Extractions: Sotosin oireyhtymä on ilmeisesti sangen monimutkaisesti perinnöllinen sairaus. Se aiheuttaa liikakasvua ja useimmiten lievää tai keskitasoista kehitysvammaisuutta Sotosin oireyhtymässä lapset ovat jo syntyessään suurikokoisia. Pää on huomattavan iso, silmät etäällä toisistaan ja leuka eteentyöntynyt. Liikakasvu on varhaislapsuudessa merkittävää, mutta se tasaantuu vähitellen, joskin tautia sairastavat ovat myös aikuisiässä normaalia kookkaampia. Lapsuudessa saattaa esiintyä syömisvaikeuksia ja tavanomaista enemmän tulehduksia. Erityisesti korvat ovat arat. Sotosin oireyhtymää sairastavat ovat yleensä kömpelöitä. Lisäksi heillä esiintyy tavanomaista useammin epilepsiaa ja kasvaimia (mm. Wilmisin tuumoria Tautia sairastavien kuntoutumisedellytykset ovat yleensä verrattain hyvät. Taudista käytetään myös jättiläismäisyyteen viittaavaa nimitystä serebraaligigantismi. Tauti on harvinainen. Sairastuneita tunnetaan koko maailmassa vain noin 150. Keskeisten oireiden tilastollinen esiintyminen oireyhtymässä on seuraavanlainen: isokokoisuus 100% ulkoneva otsa (96%) korkea kitalaki (96%) etäällä toisistaan sijaitsevat silmät (91%) pitkät kädenvarret (91%) pitkänomainen kallo (90%) kehitysvammaisuus (keskim. ÄO = 72) - 84%
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