41. Aase Syndrome - SWMC Serving Vancouver Washington Portland Oregon aase syndrome Online Medical Encyclopedia courtesy of Southwest WashingtonMedical Center, a Top 100 Hosptital award winner locacted in Vancouver, http://www.swmedicalcenter.com/110401.cfm

@import url(default.css); Health Information Manager Back to Health Library Print This Page Email to a Friend Aase syndrome Definition: 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. Symptoms: Mildly slowed growth Pale skin Delayed closure of fontanelles (soft spots) Narrow shoulders Triple jointed thumbs, absent or small knuckles, decreased skin creases at finger joints Inability to fully extend the joints from birth (congenital contractures) Cleft palate Deformed ears Droopy eye lids 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). X-rays will show skeletal abnormalities as described above.

42. - 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

@import url(default.css); Health Information Manager provided by Articles 1-10 of 1596 currently displayed. Use the Search, Topic and A-Z options below to refine your search further. Search Articles Within Current Results Search Tips Back to Health Library Complete Index Injury ... Medical Tests All A B C D ... Aarskog syndrome 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 .

43. Health/Conditions And Diseases/Genetic Disorders/Aase Syndrome -- The Doctors Lo Ask the doctor. Get free medical consultation and advice. Choose a medicalspecialist and post your question! Doctors in all medical fields are available. http://www.thedoctorslounge.net/dir/Health/Conditions_and_Diseases/Genetic_Disor

Advertisement Powered by Careerbuilder Search for: Home Humor Advertising Contact ... Links Specialties Cardiology Chest diseases Dermatology Endocrinology ... Urology Other Sections Membership Research Tools Medical Tutorials Medical Software ... Specialized Centers Headlines: The Medical Website Directory Popular Categories Popular Links Web Sites Adam.com: An Overview A definition of Aase syndrome with a brief discussion on causes, incidence and risk factors. url: www.nlm.nih.gov/medlineplus/ency/article/001662.ht... NORD: Aase Syndrome A look at the alternate names, a general discussion and resources. url: www.rarediseases.org/search/rdbdetail_abstract.htm... Pediatric Database A definition of Aase syndrome,the epidemiology, pathogenesis, clinical features, investigations and management. url: www.icondata.com/health/pedbase/files/AASESYND.HTM mozilla.org url: mozilla.org/ More Search All the Web AltaVista Gigablast Google USENET ... Yahoo In association with ODP Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor Are you a physician or a nurse?

44. 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

Medical Directory - Information about Aase syndrome About Us FAQs Home Home ... Disease . Aase syndrome Information about Aase syndrome 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 Mildly slowed growth Pale skin Delayed closure of fontanelles (soft spots) Narrow shoulders Triple jointed thumbs, absent or small knuckles, decreased skin creases at finger joints Inability to fully extend the joints from birth (congenital contractures) Cleft palate Deformed ears Droopy eye lids 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).

45. EMedicine - Holt-Oram Syndrome : Article By Craig T Basson, MD, PhD aase syndrome Fanconi anemia Roberts syndrome Thrombocytopenia with absence ofradius syndrome Vertebral defects, anal atresia, tracheoesophageal fistula http://www.emedicine.com/med/topic2940.htm

(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 Holt-Oram Syndrome 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 Author: Craig T Basson, MD, PhD , Director of Molecular Cardiology Laboratory, Assistant Professor, Department of Internal Medicine, Division of Cardiology, New York Hospital, Cornell University

46. EMedicine - Hand, Congenital Hand Deformities : Article By D Glynn Bolitho, MD, aase syndrome Triphalangeal thumb and aplastic anemia. Nager syndrome - Preaxialaplasia associated with mandibulofacial dysostosis (Treacher Collins http://www.emedicine.com/plastic/topic298.htm

(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 Hand, Congenital Hand Deformities 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 Author: D Glynn Bolitho, MD, PhD, FACS

47. 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

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

48. 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

Snowfox Home Automated Web Directory Powered by the Snowfox Relevance Engine root health medicine Aase syndrome Snowfox alphabetic index

49. 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

50. 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

51. 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

Health News Health Library Health Topics Healthy Living ... Nutrition Information on diseases and health concerns, including symptoms, treatment options, and prevention. Aase Syndrome Synonyms Disorder Subdivisions General Discussion Resources ... For a Complete Report Important 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. Synonyms Aase-Smith Syndrome II Congenital Anemia and Triphalangeal Thumbs Hypoplastic Anemia-Triphalangeal Thumbs, Aase-Smith Type Disorder Subdivisions None General Discussion 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. Resources March of Dimes Birth Defects Foundation 1275 Mamaroneck Avenue White Plains, NY 10605

52. 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

53. 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

54. 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

55. 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

56. 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

57. 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

58. TheFetus.net - Heart-hand Syndrome, Type 1 -Kathleen Helton, MD*, Luis F. Gonça Thrombocytopenia with absent radii (TAR) syndrome. aase syndrome. Trisomy 18.VACTERL association. Radial raychoanal atresia. Baller-Gerold syndrome http://www.thefetus.net/page.php?id=419

59. 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

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.uwcm.ac.uk/uwcm/mg/search/6118451.html NORD - Dyschondrosteosis 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) .. http://www.netnet.net/mums/mum_k-l.htm

60. Smith’s Recognizable Patterns Of Human Malformation, 6th Edition AdamsOliver Syndrome Holt-Oram Syndrome Levy-Hollister Syndrome FanconiPancytopenia Syndrome Radial Aplasia–Thrombocytopenia Syndrome aase syndrome http://www.intl.elsevierhealth.com/catalogue/title.cfm?ISBN=0721606156

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

Page 3     41-60 of 98    Back | 1  | 2  | 3  | 4  | 5  | Next 20