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Russell Silver Syndrome: more detail

Silver-Russell Syndrome - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References by Icon Health Publications, 2004-06-09
Russell-Silver syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Paul Johnson, 2005
Growth Disorders: Achondroplasia, Dwarfism, Acromegaly, Primordial Dwarfism, Psychosocial Short Stature, Midgetville, Silver-russell Syndrome

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Non-Mendelian Inheritance Lesson 2: Genomic Imprinting
2.3.2 russellsilver syndrome. Characterized by intrauterine growth retardationwith postnatal growth deficiency. Individuals have proportionately short
http://152.16.198.53/GeneticsModules/Design/Print.asp?CourseNum=2&LessonNum=2
Silver-Russell Syndrome
silverrussell syndrome. RSS. russell-silver syndrome The spectrum ofsilver-russell syndrome a clinical and molecular genetic study and new diagnostic
http://www.gfmer.ch/genetic_diseases_v2/gendis_detail_list.php?cat3=472
The Health Library Genetics And Birth Defects
russellsilver syndrome. russell-silver syndrome (RSS)NORD russell-silversyndromeMAGIC russell-silver syndromeGeneReviews. Seckel syndrome
http://healthlibrary.stanford.edu/resources/internet/bodysystems/genetic_dwarfis

Extractions: Diseases and Disorders Use these links to jump directly to your topic of interest in Genetics and Birth Defects: Genetics: General Genetics Gene Therapy Genetic Counseling Genetic Testing ... Genetics of Specific Diseases Birth Defects: General Birth Defects Cardiovascular Defects Connective Tissue Disorders Craniofacial Anomalies ... S - W Dwarfism (Jump to: General Information 3-M Syndrome Achondroplasia Chondrodysplasia ... Other Types of Dwarfism General Information Frequently Asked Questions (about Dwarfism):Little People of America The MAGIC Foundation Kathryn and Alan C. Greenberg Center for Skeletal Dysplasias, Johns Hopkins Dwarfism:MedlinePlus 3-M Syndrome 3-M Syndrome:Madisons Foundation 3-M Syndrome:GeneReviews Achondroplasia Achondroplasia:March of Dimes Achondroplasia:Human Growth Foundation Patient Guide to Achondroplasia:Johns Hopkins Orthopaedic Surgery Achondroplasia:Greenberg Center for Skeletal Dysplasias ... SADDAN:Genetics Home Reference, NLM Chondrodysplasia Overview Chondrodysplasia:Merck Manual Chondrodysplasia Punctata Chondrodysplasia Punctata, Autosomal Dominant:OMIM, NCBI
Russell-Silver Syndrome
,?russellsilver syndrome?russell-silversyndrome(RSS)?silver-russell syndrome?silver syndrome?
http://www.vghtpe.gov.tw/~ped/new_page_131.htm

Extractions: Russell-Silver syndrome ¦¦b Silver Âå®v¤Î Russell Âå®v¤À§O³ø§i¤F¤@¸s¦b¤l®c¤º¥Íªø¿ðº¢ ( IUGR, intrauterine growth retardation ) ªº¨àµ£¡A¦P®É¨ã¦³¨§÷¸G¤p¡BÁy¤p§e¤T¨¤§Î¡B§C¦ì¦Õ¡B²Ä¤¤â«üÅs¦±µ¥¯S¼xªº¯e¯f¡A¦]¦¹©R¦W¬° Russell-Silver syndrome ¡C Russell-Silver syndrome( RSS) ¤SºÙ¬° Silver-Russell syndrome Silver syndrome ¡C RSS P¯fì¦]¤Î¿ò¶Ç¼Ò¦¡ RSS ¦³¦hºØ¿ò¶Ç¼Ò¦¡¡A³q±`¨S¦³®a±Ú¥v¡A´¶¹M¤W§¡¬O®a±Ú¤¤ªº³æ¤@®×¨Ò¡C¦ôp¦³ RSS ±wªÌ¬O¦]¬°²Ä ¹ï¬V¦âÅé¥À·½³æ¿Ë¤GÅé¯g (maternal uniparental disomy) ¡A¥t¦³¤Ö©ó RSS ±wªÌ¦b¬V¦âÅé RSS ªº¤À¤l¿ò¶Ç¾÷¨î¤´¥¼©ú®Ô¡A´XÓ¹s¬PÓ®×Åã¥Ü¥i¯à©M¦ì©ó²Ä¤C¹ï¬V¦âÅé¤W 7p11.2 ¡V p12 GRB10 (human growth factor receptor-bound protein 10) ªº°ò¦]¦³ö¡C¥Dn¦³¤U¦C¤TºØ¿ò¶Ç¼Ò¦¡¡G ¨âÓ²Ä¤C¹ï¬V¦âÅé§¡¨Ó¦Û©ó¥À¿Ë¡A§Y©Ò¿×ªº¥À·½³æ¿Ë¤GÅé¯g (maternal uniparental disomy ¡AÂ²ºÙ UPD) ¡A¤j¬ù ªº®×¨ÒÄÝ©ó³oºØ¿ò¶Ç¼Ò¦¡¡C¦ýµ´¤j¦h¼Æ§¡¬°°¸µo©Ê¡A´X¥G©Ò¦³®×¨Ò§¡¬O®a±Ú¤¤°ß¤@ªºÓ®×¡C YÄÝ©ó¦¹ºØ¼Ò¦¡¡A«h®a±Ú¦¨ûµo¥Í¤§¾÷²v¦p¤U¡G (a) Ó®×¤§¤÷¥À¡G¤÷¥ÀÂù¤è§¡¥¼±w¯f¡C (b) Ó®×¤§¥S§Ì©n©f¡G¥S§Ì©n©fµo¯f¤§¾÷²v»P¤@¯ë¤HµL²§¡C (c) Ó®×¤§¤l¥N¡G¤l¥N¦Aµo¤§¾÷²v¤£°ª¡A¥Ø«e¨µL¥ô¦ó¤l¥N¦Aµo¾÷²v¤§¼Æ¾Ú¡C (d) ¨ä¥L¤§®a±Ú¦¨û¡Gµo¯f¤§¾÷²v»P¤@¯ë¤HµL²§¡C °£¦¹¤§¥~ªºÓ®×«h¬O¦h«ì¦]©Ò³y¦¨¡C¦b¸ß°Ý®a±Ú¥v®É¥²¶·¥]¬A¤÷¥À¤Î¥S§Ì©n©f¥X¥Í®Éªº¨°ªÅé«¡AY®a±Ú¤¤§¡µL¨ä¥L¤H±w¯f¡A«h§¡ÄÝ°¸µo©Ê¡C
Syndrome De Silver Russell
Translate this page Le syndrome de silver Russel description et prise en charge. Service de PédiatrieCliniques St Luc Bruxelles.
http://www.pediatrie.be/Silver_ Russel.htm

Extractions: Dr. D. Hermans , L.Beauport A . Définition et Incidence Le syndrome de Silver Russell associe un retard de croissance intra-utérin sans croissance de rattrapage postnatale, avec plusieurs caractéristiques morphologiques et une asymétrie des membres. On ne connaît pas précisément lincidence de ce syndrome mais elle se situe entre 1/50.000 à 1/100.000 naissances vivantes et plus de 500 cas sont rapportés dans la littérature (1). B. Symptomatologie De nombreuses caractéristiques ont été décrites dans le syndrome de Silver Russell et expliquent la grande diversité phénotypique qui le caractérise (2,3). Les signes suivants se retrouvent dans la majorité des enfants présentant cette maladie: Petit poids à la naissance avec absence de rattrapage de croissance pendant les deux premières années de la vie Un rapport poids/taille insuffisant mais avec un périmètre crânien généralement normal pour lâge Une insuffisance ou une absence total dappétit lié à un fonctionnement anormal des récepteurs à la sérotonine au niveau du système nerveux central Asymétrie corporelle Visage triangulaire front large et bombé , pseudohydrocéphalie, hypoplasie du menton et du milieu de la face, coins de la bouche tournés vers le bas et lèvre supérieure mince, palais ogival, microdontie, oreilles bas implantées et en rotation postérieure ou oreilles saillantes (cfr photos
Russell-Silver Syndrome, Eastern Carolina
russellsilver syndrome - University Health Systems of Eastern Carolina servestarboro, ahoskie, edento, winsor, maxhead, dear county, outebanks counties in
http://www.uhseast.com/117964.cfm

Extractions: Information about national and local self-help organizations and support groups. This information is provided as a resource and does not constitute an endorsement for any group. It is the responsibility of the reader to decide whether a group is appropriate for his/her needs. For evidence-based information on diseases, conditions, symptoms, treatment and wellness issues, continue searching this site. National network. Founded 1989. The above information was "verified" as correct on the date at the end of each entry. Since American Self-Help Group Clearinghouse's database is extensive but staffing is limited and information for these organizations can change, it is not possible to keep every entry in American Self-Help Group Clearinghouse database completely current and accurate. Please check with the organizations listed for the most current information.
Rarelink.net - Diagnoselisten Silver-Russells Syndrom (Russell
silverrussells syndrom (russell-silver syndrome) silver-russell syndrome;russell-silver syndrome; SRS, silver-russells syndrom
http://www.rarelink.no/diagnosedetail.jsp?diagnoseId=248&synonymId=443
Laran.waisman.wisc.edu/fv/www/lib_rss.htm
silverrussells syndrom - Små och mindre kända handikappgrupperCraniofacial and dental characteristics of silver-russell syndrome. Growth hormone therapy in silver russell syndrome 5 years experience of the
http://laran.waisman.wisc.edu/fv/www/lib_rss.htm
Rarelink.net - Diagnoselisten Silver-Russell Syndrom (Russell
silverrussell syndrom (russell-silver syndrome) silver-russell syndrome;russell-silver syndrome; SRS, silver-russells syndrom
http://www.rarelink.dk/diagnosedetail.jsp?diagnoseId=248&synonymId=443
Swiss Society Of Neonatology
We present the case of a girl with suspected silverrussell syndrome (SRS). russell-silver syndrome. In Smith s Recognizable Patterns of Human
http://www.neonet.ch/cotm/html/body_case-june03.html

Extractions: Clinic of Neonatology, University Hospital Zurich, Switzerland We present the case of a girl with suspected Silver-Russell syndrome (SRS). SRS is a rare, clinically and genetically heterogeneous disorder involving intra-uterine and post-natal growth retardation with a wide spectrum of additional dysmorphic features. Because of the clinical heterogeneity, diagnosis can be rather subjective and is not always easy to confirm. Case presentation The girl, third child of a 30-years-old mother, was born prematurely at 31 6/7 weeks of gestation by caesarean section because of a pathologic CTG. Intrauterine growth retardation had been diagnosed at 26 6/7 weeks of gestation. At that time, amniocentesis and TORCH serologies were performed with inconspicuous results.
Musculoskeletal Diseases
About the russellsilver syndrome M Cowger - Magic Foundation (US). russell-silversyndrome - an overview - MedlinePlus/ADAM
http://www.mic.ki.se/Diseases/C05.html

Extractions: Diseases and Disorders Links pertaining to Musculoskeletal Diseases Alert! Patients and laypersons looking for guidance among the target sources of this collection of links are strongly advised to review the information retrieved with their professional health care provider. Start Page Contents: Achondroplasia Achondroplasia Acquired Hyperostosis Syndrome Acrocephalosyndactylia ... Tietze's Syndrome Musculoskeletal Diseases Textbook of Orthopaedics [CR Wheeless] Educational textbook syllabus [Borrill et al.] - Orthoteers (UK) The Belgian OrthoWeb - (BE) Site Map of the Orthopaedics and Sports Medicine resource at Univ of Washington, Seattle (US) The American Academy of Orthopaedic Surgeons A Musculoskeletal Atlas , an illustrated Musculoskeletal Glossary , and a set of educational cases (radiol.) - U of Washington (US) Ortho Supersite OrthoLinx WorldOrtho including A Simple Guide to Orthopaedics [RL Huckstep] - Nepean Hosp., Sydney (AU) A collection of Case discussions at OrthoGate.org
Human EGFR, A Candidate Gene For The Silver-Russell Syndrome, Is Biallelically E
The European Journal of Human Genetics is the official Journal of the EuropeanSociety of Human Genetics, publishing highquality, original research papers,
http://www.nature.com/doifinder/10.1038/sj.ejhg.5200179

Extractions: NATURE.COM NEWS@NATURE.COM NATUREJOBS NATUREEVENTS ... Help SEARCH my account e-alerts subscribe register ... Site features NPG Subject areas Access material from all our publications in your subject area: Biotechnology Cancer Chemistry NEW! Dentistry Development Drug Discovery Earth Sciences ... Physics March 1998, Volume 6, Number 2, Pages 158-164 Table of contents Previous Abstract Next PDF Original paper Human EGFR , a candidate gene for the Silver-Russell syndrome, is biallelically expressed in a wide range of fetal tissues Emma L Wakeling 1,2,a , Sayeda N Abu-Amero , Philip Stanier , Michael A Preece and Gudrun E Moore Action Research Laboratory for the Molecular Biology of Fetal Development, Division of Paediatrics, Obstetrics and Gynaecology, Imperial College School of Medicine, Queen Charlotte's and Chelsea Hospital, London, UK Institute of Child Health, University of London, UK a Correspondence: Dr E Wakeling, Action Research Laboratory for the Molecular Biology of Fetal Development, Division of Paediatrics, Obstetrics and Gynaecology, Imperial College School of Medicine, Queen Charlotte's and Chelsea Hospital, Goldhawk Road, London W6 0XG, UK. Fax: +44 181 383 1838; Tel: +44 181 383 3533;E-mail: e.wakeling@rpms.ac.uk Abstract Maternal uniparental disomy of chromosome 7 (mUPD7) has been reported in around 10% of cases of Silver-Russell syndrome (SRS). This suggests that at least one gene on chromosome 7 is imprinted and involved in the pathogenesis of this condition. One candidate is epidermal growth factor receptor (
Human Genetics - UPD Maternal Chromosome 7
(1995) Uniparental disomy 7 in silverrussell syndrome and primordial growthretardation. Hum Mol Genet 4( 4) 583-7 Abstract
http://genes.uchicago.edu/upd/upd7m.html

Extractions: Chromosome 7. The maternal chromosome is shown on the left. An imprinting effect is certain. Annotated UPD Reference List for Maternal Chromosome 7 Eggerding, F. A.;Schonberg, S. A.;Chehab, F. F.;Norton, M. E.;Cox, V. A.;Epstein, C. J. (1994): Uniparental isodisomy for paternal 7p and maternal 7q in a child with growth retardation. Am J Hum Genet 55( 2): 253-65 Abstract Eggermann, T.;Wollmann, H. A.;Kuner, R.;Eggermann, K.;Enders, H.;Kaiser, P.;Ranke, M. B. (1997): Molecular studies in 37 Silver-Russell syndrome patients: frequency and etiology of uniparental disomy. Hum Genet 100( 3-4): 415-9 Abstract Kalousek, D. K.;Langlois, S.;Robinson, W. P.;Telenius, A.;Bernard, L.;Barrett, I. J.;Howard-Peebles, P. N.;Wilson, R. D. (1996): Trisomy 7 CVS mosaicism: pregnancy outcome, placental and DNA analysis in 14 cases. Am J Med Genet 65( 4): 348-52 Abstract Kotzot, D.;Schmitt, S.;Bernasconi, F.;Robinson, W. P.;Lurie, I. W.;Ilyina, H.;Mehes, K.;Hamel, B. C.;Otten, B. J.;Hergersberg, M.;et al. (1995): Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation. Hum Mol Genet 4( 4): 583-7 Abstract Langlois, S.;Yong, S. L.;Wilson, R. D.;Kwong, L. C.;Kalousek, D. K. (1995): Prenatal and postnatal growth failure associated with maternal heterodisomy for chromosome 7.
Blackwell Synergy - Cookie Absent
The russell silver syndrome A Case Report and Brief Review of the Literature Abstract The russell -silver syndrome s phenotypic features consist of
http://www.blackwell-synergy.com/doi/abs/10.1046/j.1525-1470.2002.00230.x

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Prices for plastic cosmetic reconstructive surgery. Prices may varry from regionto region, doctor to doctor, clinic to clinic, the prices are just approx.
http://www.civoc.com/russel_silver_syndrome.htm

Extractions: var sc_project=269223; var sc_invisible=1; Russel Silver Syndrome Cosmetic Surgery Index Abdomen Acne Scar Removal Breast ... Wrinkle Correction Rusell-Silver syndrome is a congenital disease present at birth, characterized by short stature and, frequently, asymmetry in the size of the two halves or other parts of the body. Genetic problems are thought to cause this syndrome, although the specific genes remain to be discovered. There is no specific treatment for Russell-Silver syndrome. If treated properly, many will improve in growth and appearance. There is normal intelligence. Be sure to check out the Ultimate Mega-Commi$$ion Club - NoBSzone.com! They do the research, you profit! And, their unique "Matrix Shuffle" system ensures EVERYONE has the chance to earn! Web www.civoc.com Recommended Web Sites Before you pack your bags Prices ... Pictures Before and After
Syndrome De Silver-Russel - WikipÃ©dia
Translate this page Le syndrome de silver-Russel associe un retard de croissance commençant en périodefoetale et se continuant en période post natale associé à un dymorphisme
http://fr.wikipedia.org/wiki/Syndrome_de_Silver-Russel

Extractions: modifier La pr©valence est inconnue bien que plus de 500 observations existent. modifier L'enfant la naissance pr©sente une hypotrophie importante.Des hypoglyc©mies sont fr©quentes avec des sueurs abondantes. La croissance est harmonieuse mais la taille de l'adulte est de 150 centim¨tres chez les hommes et de 140 centim¨tres chez les femmes Chez les hommes existent souvent de petites anomalies g©nitales et les enfants pr©sentent souvent des troubles digestifs modifier modifier Retard de croissance apparaissant en p©riode foetale Poids de naissance inf©rieur deux d©rivations standards Taille de naissance inf©rieure deux d©rivations standards

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