- SWMC Serving Vancouver Washington Portland Oregon Health Information Encyclopedia, aase syndrome 05/20/2004 aase syndrome is arare, inherited disorder characterized by anemia with some joint and skeletal http://www.swmedicalcenter.com/110441.cfm
Extractions: Aarskog syndrome is an inherited disease characterized by short stature , facial abnormalities, musculoskeletal, and genital anomalies. Causes, incidence, and risk factors: Aarskog syndrome is an x-linked recessive genetic disorder. This disorder affects mainly males, although females may have a milder manifestation of some of the features. It is caused by mutations in a gene called FGDY1 found on the X chromosome. Aase syndrome Aase syndrome is a rare, inherited disorder characterized by anemia with some joint and skeletal deformities. Alternative Names: Aase-Smith syndrome Causes, incidence, and risk factors: Aase syndrome is thought to be an autosomal dominant inherited disorder. The genetic basis of the disease is not known. The anemia is caused by underdevelopment of the bone marrow, which is where blood cells are formed. Abdominal aortic aneurysm Abdominal aortic aneurysm is an abnormal ballooning of the abdominal portion of the aorta, which is the major artery from the heart. Alternative Names: Aneurysm - aortic Causes, incidence, and risk factors: Abdominal aortic aneurysm involves a dilation, stretching, or ballooning of the aorta. The exact cause is unknown, but risk factors include atherosclerosis and hypertension .
Medical Directory - Information About Aase Syndrome Medical Directory Information about aase syndrome. About Us Privacy Policy FAQs Home. Home . Medical Directory . Disease . aase syndrome http://www.sainetsympa.com/ListingMedicalDirectory-A-1647.htm
Extractions: Alternative names Aase-Smith syndrome Definition Aase syndrome is a rare, inherited disorder characterized by anemia with some joint and skeletal deformities. Causes, incidence, and risk factors Aase syndrome is thought to be an autosomal dominant inherited disorder. The genetic basis of the disease is not known. The anemia is caused by underdevelopment of the bone marrow, which is where blood cells are formed. Symptoms Signs and tests A CBC (complete blood count) will show anemia and a decrease in the white blood cell count An echocardiogram may reveal heart defects (ventricular septal defect is most common).
Extractions: (advertisement) Home Specialties Resource Centers CME ... Patient Education Articles Images CME Patient Education Advanced Search Consumer Health Link to this site Back to: eMedicine Specialties Medicine, Ob/Gyn, Psychiatry, and Surgery Cardiology Last Updated: June 4, 2004 Rate this Article Email to a Colleague Synonyms and related keywords: heart-hand syndrome, hand-heart syndrome, heart hand syndrome, hand heart syndrome, congenital heart defect, congenital cardiac defect, atrial septal defect, ASD, ventricular septal defect, VSD, thumb abnormality, heart malformation, upper limb malformation, pseudothalidomide syndrome, carpal bone malformation, carpal bone fusion, carpal bone abnormality, inherited cardiovascular disease, inherited heart disease, inherited cardiac disease, Eisenmenger syndrome AUTHOR INFORMATION Section 1 of 11 Author Information Introduction Clinical Differentials ... Bibliography
Extractions: (advertisement) Home Specialties Resource Centers CME ... Patient Education Articles Images CME Patient Education Advanced Search Consumer Health Link to this site Back to: eMedicine Specialties Plastic Surgery Hand Last Updated: October 21, 2002 Rate this Article Email to a Colleague Synonyms and related keywords: limb anomaly, apical ectodermal ridge, AER, radial dysplasia, constriction bands, Holt-Oram syndrome, VATER syndrome, Fanconi syndrome, TAR syndrome, Aase syndrome, Nager syndrome, Treacher Collins syndrome, Roberts syndrome, intercalated phocomelia, amelia, phocomelia, acheiria, adactyly, absence of hand, absence of fingers, preaxial deficiency, cleft hand, syndactyly, Apert syndrome, Poland syndrome, acrosyndactyly, symphalangism, radioulnar synostosis, flexion deformities, camptodactyly, arthrogryposis, clinodactyly, delta phalanx, duplication, mirror hand, ulnar dimelia, macrodactyly, arthrogryposis multiplex congenita AUTHOR INFORMATION Section 1 of 8 Author Information Embryology And Incidence Dysmorphology Classification ... Bibliography
Myringotomy All you need to know about aase syndrome. Service descriptions, data base, prices,procedures, links, recommondations, etc will help you to make your http://www.civoc.com/aase.htm
Extractions: var sc_project=269223; var sc_invisible=1; Aase syndrome Cosmetic Surgery Index Reconstructive Surgery General Surgery Anesthesia ... Thoracotomy CIVOC provides easy to understand information for common and specific surgical procedures and organizes the information so that you and your family can understand each procedure and help you ask your physician questions. Web www.civoc.com Aase syndrome is a rare genetic disorder that may be detected during early infancy. The disorder is primarily characterized by the presence of three bones (phalanges) within the thumbs (triphalangeal thumbs) rather than the normal two and abnormally reduced production of red blood cells (hypoplastic anemia). In some instances, additional abnormalities may be present. The exact cause of Aase syndrome is unknown. However, most evidence suggests that the disorder is inherited as an autosomal recessive trait. Recommended Web Sites Prices Pictures Before and After
Automated Web Directory: Aase Syndrome root health medicine branches_of_medicine_and_dentistry conditions_and_diseases aase syndrome. Snowfox alphabetic index http://www.snowfox.com/topictrees/English/root/health/medicine/branches_of_medic
Rare Diseases Terms - Office Of Rare Diseases Additional information about aase syndrome is available from.http//www.nlm.nih.gov/medlineplus/ency/article/001662.htm http://ord.aspensys.com/asp/diseases/diseaseinfo.asp?ID=2
Rare Diseases Terms - Office Of Rare Diseases Synonyms, Ripperger aase syndrome. Links to disease information are being addedon a regular basis, so please check back often. The following databases may http://ord.aspensys.com/asp/diseases/diseaseinfo.asp?ID=2227
Aase Syndrome Synonyms, Eastern Carolina aase syndrome Synonyms University Health Systems of Eastern Carolina servestarboro, ahoskie, edento, winsor, maxhead, dear county, outebanks counties in http://www.uhseast.com/111875.cfm
Extractions: It is possible that the main title of the report Aase Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Aase syndrome is a rare genetic disorder that may be detected during early infancy. The disorder is primarily characterized by the presence of three bones (phalanges) within the thumbs (triphalangeal thumbs) rather than the normal two and abnormally reduced production of red blood cells (hypoplastic anemia). In some instances, additional abnormalities may be present. The exact cause of Aase syndrome is unknown. However, most evidence suggests that the disorder is inherited as an autosomal recessive trait. March of Dimes Birth Defects Foundation
Opera Directory A definition of aase syndrome with a brief discussion on causes, NORD AaseSyndrome. A look at the alternate names, a general discussion and resources. http://portal.opera.com/directory/?cat=524987
Medisurf - Medisurf's Categories aase syndrome / About aase syndrome. Alternative Names, Definition, Causes,Incidence, And Risk Factors. Abetalipoproteinemia, IowaClinic http://www.medisurf.com/Category/category.asp?GENE_NO=D025
Geneticalliance.org National Organization for Rare Disorders (NORD) aase syndrome MEDLINEplus -aase syndrome Pediatric Database - aase syndrome http://www.geneticalliance.org/ws_display.asp?filter=resources_by_disease&keywor
Geneticalliance.org Online Mendelian Inheritance in Man (OMIM) aase syndrome Online MendelianInheritance in Man (OMIM) - Aase-Smith syndrome http://www.geneticalliance.org/ws_display.asp?filter=resources_by_disease&keywor
Aase Syndrome D Translate this page Base de données sur les maladies rares et les médicaments orphelins. http://www.orpha.net/static/FR/aase_syndrome_d.html
Dorlands Medical Dictionary aase syndrome (aase syndrome) (ahz) Jon Morton Aase, American pediatrician, born1936 see under syndrome. AAV (AAV) adenoassociated virus; http://www.merckmedicus.com/pp/us/hcp/thcp_dorlands_content.jsp?pg=/ppdocs/us/co
Leri Weill Search Results (January 2000) Database RDB 5 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 5 5Oxoprolinuria A Aarskog Syndrome aase syndrome Ablepharon Macrostomia Syndrome http://www.ilizarov.org.uk/leri.htm
Extractions: The following is a list of sites discovered relating to Leri Weill Syndrome and other aspects of dwarfism. SHOX - Short stature homeobox Gene symbol : SHOX Location : Xp Mutations in this gene were first reported in 1997 Rao (1997) Nat Genet 16, 54 Number of entries by mutation type Click on the respective mutation type to view detailed information about the... http://www.stepstn.com/nord/rdb_sum/888.htm NHGRI Homeodomain Resource: Mutation Submission Form - Homeodomain Home Submit Mutation Data Protein Name Mutation Name Map Location Nucleotide Position Codon Number Exon Number Intron Number Wild type DNA sequence at above postion Mutated DNA sequence at above postion At DNA/RNA level Deletion, in... http://genome.nhgri.nih.gov/homeodomain/submission MUMS: List of Disorders - "K - L" - MUMS: List of Disorders K - L Kabuki Make-up Syndrome (13) * Kallmann Syndrome (DeMorisier Dysplasia Olfactorgenitalis) (1) * Kartagener Syndrome (5)Kasabach-Merritt (1) Kawasaki Disease (8) Kearns-Sayre Syndrome (5)Keratoconus (cornea disorder) ..
