Home  - Health_Conditions - Sotos Syndrome

Books Baby Camera Phones Computers Games DVD Electronics Kitchen Magazines Music Garden Software Tools Toys Video Apparel & Accessories Jewelry & Watches Musical Instruments Health & Personal Care Beauty Sports & Outdoors Office Products

e99.com Bookstore

Images

Newsgroups

41-60 of 91    Back | 1  | 2  | 3  | 4  | 5  | Next 20

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

Sotos Syndrome:     more detail

The Official Parent's Sourcebook on Soto's Syndrome: Directory for the Internet Age by Icon Health Publications, 2005-01-31 Sotos syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Cindy, CGC Hunter, 2005 Sotos syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Neurological Disorders</i> by Cindy, CGC Hunter, 2005 Sotos Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-20 Sotos syndrome: A handbook for families by Rebecca Rae Anderson, 2000 Sotos Syndrome by John Ed. Anderson, 1999-01 The Physical Lincoln Complete by John G. Sotos, 2008-09-26 Consanguineous Marriages in the American Population by George B. Louis Arner, 2010-08-10 Anomalies And Curiosities Of Medicine- George M. Gould, A.M., M.D. by A.M., M.D. George M. Gould, 2010-02-17

lists with details

41. Trisomy 18.... 1995
    Translate this page Titre/Title, sotos syndrome. Editeur/Editor, MacKeith Press.Lieu/Place, London, UK. Date, 1995. Collation/Series, p.186-88.  
    http://www.cidg.com/~marienf/k/i/n/m003111.htm
    
    Extractions: # Mono.: S0002812 Cote/Call Number Auteur/Author Udwin, Orlee Dennis, Jennifer Titre/Title Trisomy 18. Editeur/Editor MacKeith Press Lieu/Place London, U.K. Date Collation/Series p.194-95 Descripteurs/Descriptors Trisomie 18 Phenotype comportemental Coll.: Clinics in Developmental Medicine, No 138 Demande par

42. AD HOC BIBLIO - INDEX SUJETS LETTRE S Compilé Le 14/01/03
    sotos syndrome Cerebral gigantism .a; Parent guide to sotos syndrome a;Psychological characteristics of sotos syndrome .a;  
    http://www.cidg.com/~marienf/k/i/mid5s.htm

43. Healthfinder® — What Is Sotos Syndrome?
    What is sotos syndrome? internet URL. http//www.well.com/user/sssa/whatisit.htm.sponsoring agency. sotos syndrome Support Association. description.  
    http://www.healthfinder.gov/Scripts/ShowDocDetail.asp?doc=2278&lang=1

44. Healthfinder® — Sotos Syndrome Support Association - SSSA
    The sotos syndrome Support Association (SSSA) was organized in 1988 to providea support network for families and individuals affected by the syndrome.  
    http://www.healthfinder.gov/orgs/HR2419.htm
    
    Extractions: Wheaton, IL 60187 888-246-7772 (Voice - Toll-free) The Sotos Syndrome Support Association (SSSA) was organized in 1988 to provide a support network for families and individuals affected by the syndrome. Sotos syndrome, also known as cerebral gigantism, is a neurological brain-based disorder resulting in physical and mental developmental delays in children. The goals of the SSSA are to provide a social support environment for families and individuals with Sotos syndrome; increase public awareness and education about the disorder; and provide opportunites for professionals working with affected individuals to collect and share data for research. The SSSA has members across the United States, Canada and Great Britain, and sponsors an annual conference. What is Sotos Syndrome?

45. GeneCards Disorder Information: Sotos Syndrome
    GeneCards Disorder Information sotos syndrome Search different databasescontaining disease information by clicking on the buttons below.  
    http://www.rzpd.de/cgi-bin/cards/disodisp?Sotos syndrome

46. Perinnöllisyysklinikan Tietolehtiset Sekä Tilauslomake
    Sotosin oireyhtymästä Avainsanat (synonyymit) Sotos, Sotosin oireyhtymä, Sotosinsyndrooma, sotos syndrome, cerebral gigantism. Cole TRP. sotos syndrome.  
    http://www.vaestoliitto.fi/toimintayksikot/perinnollisyysklinikka/sisaltosivut/s
    
    Extractions: Väestöliiton perinnöllisyysklinikka 2002 Sotosin oireyhtymästä Avainsanat (synonyymit): Sotos, Sotosin oireyhtymä, Sotosin syndrooma, Sotos syndrome, cerebral gigantism Sotosin oireyhtymälle hyvin tyypillisiä ulkonäköpiirteitä ovat kupera, leveä ja korkea otsa, pitkänomainen kallon muoto, pitkä ja kärkeensä kapeneva leuka, ylöskaartuvat kulmakarvat ja hiukan alaspäin suuntautuvat luomiraot. Hiusraja on tavallista ylempänä ja nuorempana tukka on etenkin ohimoseudussa harvaa ja heikkokasvuista. Nenän, leuan ja poskien ihopunotus yleistä. Sotosin oireyhtymässä kasvu on nopeinta varhaislapsuudessa. Kasvulle ominaista on vartaloon nähden suhteellisesti pitkät raajat ja pituuteen nähden usein isot kämmenet ja jalkaterät. Vaikka lopullinenkin pituus on usein keskimääräistä suurempi ei odotettavissa kuitenkaan ole jättikasvua. Sotos tytöillä kuukautiset näyttävät tulevan hiukan keskimääräistä nuorempana kun taas Sotos-pojilla murrosikäkehitys näyttää alkavan keskimääräistä myöhemmin. Tutkittua tietoa Sotos-henkilöitten hedelmällisyydestä ei ole, harvinaisista yksittäistapauksista kertova tieto ei puhu normaaleja lapsensaantimahdollisuuksia vastaan. Sisäelinten rakennepoikkeavuudet kuten sydänviat ovat Sotosin oireyhtymässä vain vähän yleisempiä kuin väestössä keskimäärin. Varhaislapsuudessa välikorva- ja hengitystietulehdukset ovat tavallisia. Ruoansulatuselimistön tavallisia oireita ovat lisääntynyt ruokahalu ja juominen sekä ummetus. Virtsatulehduksia ja virtsan takaisinvirtausta rakosta virtsanjohtimiin (ns vesikoureteraalinen refluks, VUR) on esiintynyt noin viidenneksellä. Hoitoa vaativaa lattajalkaisuutta ja selän ryhtivirheitä voi kehittyä. Noin puolella Sotos-lapsista on epilepsiaa tai kuumekouristuksia. Nämä kohtausoireet eivät yleensä ole suuri hoito-ongelma. Silmien taittovirheet ovat tavallisia, mutta näkövammaisuus hyvin poikkeuksellista. Kuulovammaisuuskaan ei ole yleistä Sotosissa.

47. ORPHANET® : Sotos Syndrome
    Translate this page ORPHANET. ORPHANET database access. sotos syndrome. Directaccess to details Alias Cerebral gigantism. Home Page.  
    http://www.orpha.net/static/GB/sotos.html

48. Error Page
    DISEASE Vasquez hurst sotos syndrome, Synonym(s) X linked hypogonadismgynecomastia mental retardation, MIM 309590, Sign(s) of the disease (27),  
    http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=3423

49. Sotos
    sotos syndrome Infantile Giantism,. the recent scientific literature. TITLETumors and nontumors in sotos syndrome letter. AUTHOR(S) CohenMM Jr.  
    http://www.indiana.edu/~pietsch/sotos.html
    
    Extractions: return to Shufflebrain main menu A search of MEDLINE conducted at Indiana University , Bloomington, Indiana web contact: pietsch@indiana.edu The following items were compiled from MEDLINE using SilverPlatter and are presented with the latter organization's generous co-operation and permission. ( See SilverPlatter's Worldwide Library for bibliographic search information Sotos syndrome infantile (cerebral) giantism is a pre- and post-natal condition of in which a child's head and muscles grow at abnormally rapid rates and become unusually large. The cause is unknown. Record 1 of 41 in MEDLINE EXPRESS (R) 1999/01-1999/10 TITLE: Tumors and nontumors in Sotos syndrome [letter] AUTHOR(S): Cohen-MM Jr SOURCE (BIBLIOGRAPHIC CITATION): Am-J-Med-Genet. 1999 May 21; 84(2): 173-5 INTERNATIONAL STANDARD SERIAL NUMBER: 0148-7299 PUBLICATION YEAR: 1999 LANGUAGE OF ARTICLE: ENGLISH COUNTRY OF PUBLICATION: UNITED-STATES MINOR MESH HEADINGS: Adolescence-; Adult-; Child-; Child,-Preschool; Diagnosis,-Differential; Infant-; Nevus-diagnosis; Syndrome-

50. Syndrome - S
    sotos syndrome  
    http://www.erzwiss.uni-hamburg.de/personal/hoffmann/syndrome/syn-s.html
    
    Extractions: Uni Hamburg FB Erziehungswissenschaft Institut 05 Suche ... Links S YNDROME - S Symbole: = Homepage; = Aufsatz, Artikel, Monographie; = Kurzinformation. Saethre Chotzen Syndrom Schizophrenie Silver Russel Syndrom Smith Lemli Opitz Syndrom Smith Magenis Syndrom Sneddon Syndrom (Livedo Racemosa) Sotos Syndrom Spastische Spinalparalyse Spina bifida Sudeck Syndrom (Algodystrophie, Complex Regional Pain Syndrome I) Uni Hamburg FB Erziehungswissenschaft Institut 05 ... Links

51. Soto('s) Syndrome
    sotos syndrome; Soto's Syndrome; sotos syndrome; SOTOS Association;Is anyone out there dealing with a condition called sotos syndrome?  
    http://www.bdid.com/soto.htm

52. IV SPECIFIC DISABILITIES (continued)
    SMITHMAGENIS SYNDROME. PRISMS Parents Researches Interested in Smith-MagenisSyndrome. sotos syndrome. sotos syndrome USA Support Association.  
    http://www.pourhouse.com/ramp/ramp4.htm

53. Connexion
    Citations for STO 1, Haploinsufficiency of NSD1 causes sotos syndrome. 2, No evidencefor uniparental disomy as a common cause of sotos syndrome. Smith M, et al.  
    http://www.dsi.univ-paris5.fr/genatlas/tbiblio.php?symbol=STO

54. National Support Groups / Information Sites
    SmithMagenis Syndrome. PRISMS USA sotos syndrome sotos syndromeSupport Association; Families of Spinal Muscular Atrophy Home Page.  
    http://www.mostgene.org/support/s-t.htm
    
    Extractions: As scientific findings and medicine are changing rapidly, we urge you to note the date of publication of all material you view. Please consult with your health care provider regarding how any information found on the Internet may apply to your own situation. - S - Sanfilippo syndrome At the CDGS Family Network Schizencephaly 'Schiz Kidz Buddies' Scleroderma Scleroderma Research Foundation

55. Health Library - Sotos Syndrome
    Topics. Search. sotos syndrome. Self Help Clearinghouse. sotos syndromeSupport Association. International network. Founded  
    http://uhcs.universityhealth.org/library/healthguide/selfhelp/topic.asp?hwid=shc

56. Kprones BannayanID10044
    Arch Path 1971; 92 15. Medline 71233629. sotos syndrome with intestinal polyposisand pigmentary changes of the genitalia. Ruvalcaba RHA, Myhre S, Smith DW.  
    http://www.infobiogen.fr/services/chromcancer/Kprones/BannayanID10044.html
    
    Extractions: Home Genes Leukemias Solid Tumours ... NA Identity Other names Bannayan-Zonana syndrome Riley-Smith syndrome Ruvalcaba-Myhre-Smith syndrome Macrocephaly, pseudopapilledema, multiple hemangiomata Macrocephaly, multiple lipomas, hemangiomata Inheritance autosomal dominant; existence of sporadic cases Clinics Note Bannayan-Riley-Ruvalcaba syndrome is an overgrowth syndrome / hamartomatous polyposis condition with an increased risk of benign and malignant tumours; other overgrowth syndromes at (known) risk of tumourigenesis are : Beckwith-Weideman syndrome Sotos syndrome (cerebral gigantism), Hemihyperplasia (hemihypertrophy), and Simpson Golabi Behemel syndrome Phenotype and clinics onset in chilhood (in contrast with Cowden disease , although an allelic disorder, see below); more often found in male patients (lower penetrance in female patients).

57. 1917 Molecular Definition Of Del (2) (q14.1q21) In A Patient
    Molecular definition of del (2) (q14.1q21) in a patient with a Marfanoid body habitus,early features reminiscent of sotos syndrome and an attention deficit  
    http://www.faseb.org/genetics/ashg99/f1917.htm

58. Untitled
    Program Nr 2140 No evidence for PTEN mutations as a common cause ofsotos syndrome or autosomal dominant macrocephaly. S. Tomkins  
    http://www.faseb.org/genetics/ashg00/f2140.htm

59. CancerGene ARA267
    Cole TR;Rahman N NSD1 mutations are the major cause of sotos syndrome and occurin some cases of Weaver syndrome but are rare in other overgrowth phenotypes.  
    http://caroll.vjf.cnrs.fr/cancergene/CG1830.html
    
    Extractions: GDB SwissProt LocusLink Atlas of Genetics and Cytogenetics in Oncology and Haematology : Class TRANSLOC Keywords NSD gene family; PHD-finger motif; SET domain; transcriptional intermediary factor Diseases Leukemia, Myelocytic, Acute Comments The proteins of the NSD gene family [NSD1, NSD2 ( CG:971 ) , and NSD3 ( CG:1991 )] are highly similar within a block of about 700 amino acids. This block contains several conserved domains, such as the SET domain and the PHD finger, present in proteins involved in development and/or chromatin reorganization. First to be isolated was the murine Nsd1 ( UI:98292459 GenBank:AF064553 ) in a search for proteins that interact with the ligand-binding domain of retinoic acid receptor alpha (RARA, CG:158 ). NSD1, a novel 2588 amino acid mouse nuclear protein interacts directly with the ligand-binding domain (LBD) of several nuclear receptors (NRs). In addition to the conserved domains (a SET domain and multiple PHD fingers) found in both positive and negative Drosophila chromosomal regulators, NSD1 contains two distinct NR interaction domains, NID-L and NID+L, that exhibit binding properties of NIDs found in NR corepressors and coactivators, respectively. The human homologue of the mouse Nsd1 gene was isolated by Jaju et al. (2001

60. Health Library - Sotos Syndrome
    TOLL FREE. sotos syndrome. Self Help Clearinghouse. sotos syndrome SupportAssociation. International network. Founded 1984  
    http://hvlib.integris-health.com/Library/HealthGuide/SelfHelp/topic.asp?hwid=shc

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

41-60 of 91    Back | 1  | 2  | 3  | 4  | 5  | Next 20