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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

Sotos
TITLE Testicular yolk sac tumour in a patient with sotos syndrome. ABSTRACTThe cause of sotos syndrome is unknown but it usually occurs sporadically.
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-
Indian Pediatrics - Editorial
Abstract A case of cerebral gigantism (sotos syndrome) with West syndrome in a Cerebral Gigantism (sotos syndrome) is an uncommon syndrome of growth
http://www.indianpediatrics.net/july2003/july-673-675.htm

Extractions: P.D. Singhi From the Neurodevelopment Unit, Department of Pediatrics, Advanced Pediatric Center, Post Graduate Institute of Medical Education and Research, Chandigarh, India. Correspondence to: Dr. P.D. Singhi, Professor and Head, Neurodevelopment Unit, Department of Pediatrics, Post Graduate Institute of Medical Education and Research, Chandigarh 160 012, India. E-mail: medinst@pgi.chd.nic.in * Psychologist **Anthropologist Manuscript received: May 22, 2002; Initial review completed: July 18, 2002; Revision accepted: January 20, 2003. Abstract: A case of cerebral gigantism (Sotos syndrome) with West syndrome in a one year old male child is reported. The case had a large stature, typical facies and neurodevelopmental delay along with infantile spasms, which were refractory to treatment with valproate and clonazepam. Cerebral Gigantism (Sotos syndrome) is an uncommon syndrome of growth accelera-tion; macrocephaly, acromegaloid features and delay in neuropsychomotor development during infancy. Syndrome delineation and differential diagnosis are based on evaluation of phenotypic characteristics and evolutive history of patients. Extensive search of literature revealed only one reported case of Sotos syndrome with West syndrome till date(1). We hereby report another case of Sotos syndrome presenting with rare manifestation of West syndrome, the first such report from India.
Department Of Human Genetics - Clinical Laboratory And Patient Services
Kurotaki et al., Haploinsufficiency of NSD1 causes sotos syndrome (2002) Nature Douglas et al., NSD1 mutations are the major cause of sotos syndrome and
http://genes.uchicago.edu/clinic/SotosTest.html

Extractions: Thank you for your inquiry regarding NSD1 analysis for individuals with a clinical diagnosis of Sotos syndrome. Microdeletions, identifiable by FISH analysis, and mutations of the NSD1 gene have recently been identified in patients with Sotos syndrome1,2. These preliminary findings suggest that about 77% of patients with a clinical diagnosis of Sotos syndrome have either a deletion or mutation in the NSD1
Entrez PubMed
Haploinsufficiency of NSD1 causes sotos syndrome. Kurotaki N, Imaizumi K, HaradaN, Masuno M, Kondoh T, Nagai T, Ohashi H, Naritomi K, Tsukahara M,
http://www.facultyof1000.com/pubmed/11896389

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Faculty Of 1000 Biology | Haploinsufficiency Of NSD1 Causes Sotos Syndrome.
Haploinsufficiency of NSD1 causes sotos syndrome. Kurotaki N, Imaizumi K, , NiikawaN, Matsumoto N Nat Genet 2002 Apr 30(4)3656
http://www.facultyof1000.com/article/11896389
Sotos Syndrome
NSD1 Mutations Are the Major Cause of sotos syndrome and Occur in Some Cases ofWeaver Syndrome but Are Rare in Other Overgrowth Phenotypes
http://www.gfmer.ch/genetic_diseases_v2/gendis_detail_list.php?cat3=473
Arquivos De Neuro-Psiquiatria -
ABSTRACT sotos syndrome or cerebral gigantism is characterized by The mainclinical finding in sotos syndrome is prenatal and postnatal overgrowth.
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2002000200009
Arquivos De Neuro-Psiquiatria -
ABSTRACT sotos syndrome or cerebral gigantism is characterized by Bone ageis also significantly advanced in most cases of sotos syndrome,
http://www.scielo.br/scielo.php?pid=S0004-282X2002000200009&script=sci_arttext&t
Sotos Syndrome - FISH Analysis
The Kleberg Cytogenetics Laboratory offers a fluorescence in situhybridization (FISH)based assay for identifying the microdeletion of the NSD1gene (5q35)
http://www.bcmgeneticlabs.org/tests/cyto/sotos.html

Extractions: Sotos syndrome is characterized by overgrowth in infancy and early childhood, dysmorphic facial features, advanced bone age and developmental delay. The dysmorphic features typically include macrocephaly, frontal bossing, prominent jaw and down-slanting palpebral fissures. The phenotype is variable, with some individuals having major cardiac, central nervous system and urinary system anomalies. Sotos syndrome is presumed to be autosomal dominant, with the majority of cases due to new mutations. Reasons for Referral:
Soto's Syndrome
How is a Diagnosis of Soto Syndrome Made? sotos syndrome Support Association ofCanada (also in French); Other Syndromes or Disorders That are Related to
http://www.noah-health.org/en/bns/disorders/other/soto.html
What Is Sotos Syndrome? - Healthfinder®
This minifact sheet provides basic consumer information about this geneticdisorder, also known as cerebral gigantism because of the distinctive head shape
http://mentalhealth.about.com/library/h/docs/bld02278.htm

Extractions: zJs=10 zJs=11 zJs=12 zJs=13 zc(5,'jsc',zJs,9999999,'') zfs=0;zCMt='a14' About Mental Health Resources Mental Health Essentials ... Help zau(256,140,140,'el','http://z.about.com/0/ip/417/C.htm','');w(xb+xb+' ');zau(256,140,140,'von','http://z.about.com/0/ip/496/7.htm','');w(xb+xb); Sign Up Now for the Mental Health Resources newsletter!
Sotos Syndrome
Complete online version of The Encyclopaedia of Medical Imaging including textand images from The Encyclopaedia of Medical Imaging s eight book volumes
http://www.amershamhealth.com/medcyclopaedia/medical/Volume VII/SOTOS SYNDROME.a

Extractions: financial services our commitment our company Search Medcyclopaedia for: Search marked text (mark text before you click) Browse entry words starting with: A B C D ... amershamhealth.com Sotos' syndrome, (Juan Fernandez Sotos, born 1927, Spanish-born American paediatrician), the association of mental retardation with poor motor co-ordination and behavioural problems, a large head and high birth weight, and rapid growth in height and weight. Radiologically, there is a large dolichocephalic skull, large hands and feet, and an advanced bone age. There may also be kyphoscoliosis.
Resources For Genetic Counselors - Sotos Syndrome
Ø characteristic facial appearance specific to sotos syndrome Gene mutationfound in a number of Japanese patients with sotos syndrome
http://www.genesoc.com/counseling2/article153.html

Extractions: Posted on Thursday, February 10 @ 00:02:24 CST by debi Sotos Syndrome Incidence: Diagnosis: o alters in childhood and adolescence o in newborn period (macrocephaly, high bossed forehead, dolichocephaly, high palate, appearance suggestive of hypertelorism) o face lengthens, jaw becomes more prominent, dolichocephaly (tall narrow skull) and frontal bossing (prominent forehead) become more obvious
Sotos Syndrome - St. Joseph Mercy, Ann Arbor Michigan
sotos syndrome St. Joseph Mercy Health System Hospitals serving Ann Arbor, SEMichigan, Washtenaw County, Livingston County, Wayne County, Oakland County,
http://www.sjmercyhealth.org/15673.cfm
Spine - UserLogin
sotos syndrome, a rare overgrowth syndrome with slightly more than 300 cases A previously unreported cervical spine instability in sotos syndrome is
http://www.spinejournal.com/pt/re/spine/fulltext.00007632-200404010-00023.htm
Spine - Abstract: Volume 29(7) April 1, 2004 P E153-E156 Cervical Instability In
Cervical Instability in sotos syndrome A Case Report. sotos syndrome, a rareovergrowth syndrome with slightly more than 300 cases reported in the
http://www.spinejournal.com/pt/re/spine/abstract.00007632-200404010-00023.htm

Extractions: Study Design. A case report on cervical instability detected in a patient with Sotos syndrome, along with a review of the literature on Sotos syndrome and associated spinal findings. Objective. To present the case of a patient with a C3-C4 anterolisthesis occurring in the setting of Sotos syndrome and explore a possible association between the two. Summary of Background Data. Sotos syndrome, a rare overgrowth syndrome with slightly more than 300 cases reported in the English literature to date, is characterized by a unique constellation of symptoms and signs including musculoskeletal findings such as scoliosis, pes planus, generalized ligamentous laxity, and increased growth rates. Cervical instability as part of this syndrome is unreported and rarely presents as a C3-C4 anterolisthesis. Methods. A case report detailing the evaluation and treatment of a cervical instability in a 3-year-old with Sotos syndrome.
GeneReviews: Sotos Syndrome
Your browser does not support HTML frames so you must view sotos syndrome in aslightly less readable form. Please follow this link to do so.
http://genetests.org/profiles/sotos/
Child Growth Foundation Sotos
Two of these conditions are Marfan syndrome and sotos syndrome. sotos syndrome,or gigantism, usually presents in early childhood.
http://www.childgrowthfoundation.org/Sotos.htm

Extractions: London W4 1P W Registered Charity No: 274325 Tall Stature Children with tall stature, i.e. above the 99.6 th centile, are usually so because of genetic reasons - they simply have tall parents! This is referred to as constitutional tall stature. However, tall stature may also be associated with various paediatric syndromes that require specialist assessment. Two of these conditions are Marfan syndrome and Sotos syndrome. Tall stature in childhood usually presents less initial concern than short stature because, at least in early childhood, being tall can be advantageous. However, excessive tall stature can cause problems, particularly at school. It may be difficult to remember that a five-year old child who has the stature of an eight-year-old only has the educational and emotional development of a five-year old. Their size can seem inappropriate for their classroom peers and so very tall children may be labelled as clumsy or aggressive. Other treatments that reduce growth hormone secretion are being evaluated through clinical trials. As a final option, a surgical reduction of leg length is a possibility.
Clinical Dysmorphology - Abstract: Volume 13(4) October 2004 P 199-204 Clinical
In this review we will present the clinical features of sotos syndrome cases withproven This has allowed redefinition of sotos syndrome as a condition
http://www.clindysmorphol.com/pt/re/mcd/abstract.00019605-200410000-00001.htm
Clinical Dysmorphology - UserLogin
Two patients with sotos syndrome who developed a severe scoliosis are described . sotos syndrome is characterized by early overgrowth and characteristic
http://www.clindysmorphol.com/pt/re/mcd/fulltext.00019605-200204000-00009.htm

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