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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

81. OMIM - SOTOS SYNDROME
    http://www3.ncbi.nlm.nih.gov/entrez/dispomim.cgi?cmd=framedSynopsis&id=117550

82. Universiteit Van Tilburg
    1999). Unique case of sotos syndrome in an identical twin neuropsychologicalfindings of a three year followup. Paper presented  
    http://www.uvt.nl/webwijs/pub.html?anr=751995

83. J Med Genet -- KOK Et Al. 36 (4): 346
    EDITOR Involvement of region 3p21 of chromosome 3 in the development ofsotos syndrome is suggested by two patients who have been described.  
    http://www.jmedgenet.com/cgi/content/full/36/4/346
    
    Extractions: Genetics J Med Genet 346-347 ( April ) E DITOR Involvement of region 3p21 of chromosome 3 in the development of Sotos syndrome is suggested by two patients who have been described. One is a Sotos syndrome patient carrying an apparently balanced translocation t(3;6)(p21;p21). The other is a non-smoking female with Sotos syndrome who died of small cell lung cancer at 22 years of age. This type of cancer is characterised by a consistent loss of heterozygosity at 3p21.3. We were able to set up an EBV immortalised lymphoblastoid cell line from a blood sample from the patient with the t(3;6) and show by fluorescent in situ

84. ADC -- YULE 80 (5): 493
    Letters to the editor. Cancer in sotos syndrome. NonHodgkin s lymphomahas also been reported in three other patients with sotos syndrome.  
    http://adc.bmjjournals.com/cgi/content/full/archdischild;80/5/493b
    
    Extractions: Download to Citation Manager Arch Dis Child 493 ( May ) E DITOR We greatly enjoyed reading the article by Cole on overgrowth disorders in childhood. While the article alluded to the increased risk of malignant disease among children with Beckwith-Wiedeman syndrome (BWS) no mention was made of the increased risk of cancer in Sotos syndrome. We recently treated a 3 year old boy with Sotos syndrome for abdominal B cell lymphoblastic lymphoma (Murphy stage III) in accordance with United Kingdom children's cancer study group protocol 9002. Although his lymphoma exhibited only a partial response to standard chemotherapy, he remains disease free two years later following second look surgery and subsequent high dose treatment with autologous bone marrow rescue.

85. J Med Genet -- Abstracts: Rio Et Al. 40 (6): 436
    ABSTRACT sotos syndrome is an overgrowth syndrome characterised by pre and postnatalovergrowth, macrocephaly, advanced bone age, and typical facial features.  
    http://jmg.bmjjournals.com/cgi/content/abstract/40/6/436
    
    Extractions: Sotos syndrome is an overgrowth syndrome characterised by pre- and postnatal overgrowth, macrocephaly, advanced bone age, and typical facial features. Weaver syndrome is a closely related condition characterised by a distinctive craniofacial appearance, advanced carpal maturation, widened distal long bones, and camptodactyly. Haploinsufficiency of the gene has recently been reported as the major cause of Sotos syndrome while point mutations accounted for a minority of cases. We looked for

86. J Med Genet -- Abstracts: Cole And Hughes 31 (1): 20
    ARTICLES. sotos syndrome a study of the diagnostic criteria and natural history. Homepage S. P Robertson and A. Bankier sotos syndrome and cutis laxa J. Med.  
    http://jmg.bmjjournals.com/cgi/content/abstract/31/1/20
    
    Extractions: Institute of Medical Genetics, University Hospital of Wales, Heath Park, Cardiff, UK. Seventy-nine patients with a provisional diagnosis of Sotos syndrome were clinically assessed, and their photographs between the ages of 1 and 6 years evaluated. These photographs, together with photographs of first degree relatives, also at ages 1 to 6 years, were reviewed by four clinical geneticists. Forty-one probands (but no first degree relatives) were identified in whom the facial gestalt was thought to be characteristic of Sotos syndrome. Comparison of anthropometric measurements, bone age, and

87. Human Protein: Q96L73 - Nuclear Receptor Binding SET Domain Containing Protein 1
    HA, Kinoshita,A., Mizuguchi,T., Yoshiura Ki,K., Ohta,T., Kishino,T., Fukushima,Y.,Niikawa,N., Matsumoto,N., Haploinsufficiency of NSD1 causes sotos syndrome.  
    http://harvester.embl.de/harvester/Q96L/Q96L73.htm
    
    Extractions: UniProt ensEMBL Entrez RZPD ... EBI-Hinxton-"Uniprot-Swissprot-TrEMBL" database General information Entry name Accession number Created Rel. 42, 10-OCT-2003 Sequence update Rel. 42, 10-OCT-2003 Annotation update Rel. 43, 29-MAR-2004 Description and origin of the Protein Description Nuclear receptor binding SET domain containing protein 1 (NR-binding SET domain containing protein) (Androgen receptor-associated coregulator 267). Gene name(s) NSD1 OR ARA267. Organism source Homo sapiens (Human). Taxonomy Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Primates; Catarrhini; Hominidae; Homo. NCBI TaxID References Wang,X., Yeh,S., Wu,G., Hsu,C.-L., Wang,L., Chang,T., Yang,Y., Guo,Y., Chang,C.,

88. Sotos' Syndrome (www.whonamedit.com)
    sotos syndrome A syndrome of excessive growth during the first 4 to 5 years oflife, cerebral gigantism, acromegalic features, and mild mental retardation  
    http://www.whonamedit.com/synd.cfm/2464.html
    
    Extractions: This survey of medical eponyms and the persons behind them is meant as a general interest site only. No information found here must under any circumstances be used for medical purposes, diagnostically, therapeutically or otherwise. If you, or anybody close to you, is affected, or believe to be affected, by any condition mentioned here: see a doctor. Cerebral gigantism, cerebral gigantism in childhood, constitutional gigantism, gigantismus cerebralis, gigantismus constitutionalis, gigantismus idiopathicus, hypothalamic gigantism, macrostomia-mental retardation syndrome, mental retardation-overgrowth sequence, pituitary gigantism, prenatal gigantism with macrocephaly. A syndrome of excessive growth during the first 4 to 5 years of life, with cerebral gigantism and generalised large muscles in childhood, acromegalic features, and a nonprogressive cerebral disorder with nonprogressive mild mental retardation and defective coordination. After early childhood growth seems to approach normal, remaining, however, two standard deviations above means for chronological age. Birth weight and length greater than normal. Other principal features are dolicocephaly, macrocrania, hypertelorism, antimongoloid palpebral slant, high-arched palate, frontal bossing, mandibular prognathism, and precocious dentition. Occasionally, obesity, convulsions, abnormal dermatoglyphic pattern. Both sexes. Most cases are sporadic but some are transmitted as an autosomal dominant trait.

89. Sotos' Syndrome - General Practice Notebook
    sotos syndrome. sotos syndrome presents in childhood with developmentaldelay, high forehead, large hands and feet and tall for age.  
    http://www.gpnotebook.co.uk/cache/1167720489.htm

90. ORPHANET - Maladies Rares - Médicaments Orphelins
    Translate this page Version pour Impression, MALADIE sotos, syndrome de, Synonyme(s) Gigantismecérébral, CIM Q87.3, Le syndrome de sotos est une affection  
    http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=821

91. ORPHANET® : Sotos, Syndrome De
    Translate this page ORPHANET. Accès à la base de données Orphanet. sotos, syndromede. Accès direct aux détails Résumé Le syndrome de sotos est  
    http://www.orpha.net/static/FR/sotos.html

92. En Masse Sotos (syndrome De)
    Translate this page sotos (syndrome de) Voir également macrocéphalie, microcéphalie, dolicocéphalie,hypothalamus, facteur de croissance, hypertélorisme, prognathisme  
    http://www.vulgaris-medical.net/texts/sotos.htm
    
    Extractions: Hypertélorisme : malformation du crâne et du visage se caractérisant par un agrandissement de la petite aile du sphénoïde (os horizontal situé à l'intérieur du crâne, derrière les orbites, à sa partie moyenne), entraînant un agrandissement de la distance séparant les deux orbites contenant les yeux, et de la racine du nez.

93. Cerebral Gigantism (Sotos Syndrome).
    Graded Specialist (Paediatrics), INHS Dhanvantari, Port Blair. Cerebral gigantism(sotos syndrome). Medical Journal Armed Forces India. 1996 July; 52(3) 2001.  
    http://medind.nic.in/imvw/imvw11615.html

94. Sotos' Syndrome
    sotos syndrome. Author s Email cadou@trenton.edu I am asking anyoneout there who knows more1information about sotos syndrome (ie.  
    http://neuro-www.mgh.harvard.edu/neurowebforum/GeneralFeedbackArticles/SotosSynd
    
    Extractions: I am asking anyone out there who knows more1information about Sotos' Syndrome (ie. support groups for1or in France, growth and mental development expectations,1sensory-motor developement, psycho-social development, etc)1Basically, I'm interested in everything about the syndrome1and it's effects on the people and environment around them.1If *anyone* has information I would appreciate a response!1Thank you! Next Article

95. Search Results
    April 2004, (PubMed). Carlo W, et al. Cervical instability in sotossyndrome a case report. Spine. 2004 Apr 16; 29(7), pp. E1536  
    http://www.mypubmed.com/search/Search.cgi/SearchResult?Database=PubMed&IR_FreeTe

96. Redirect
    http://www.ncbi.nlm.nih.gov/htbin-post/Omim/dispmim?117550

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