61. Hand Radiographs In Russell-Silver Syndrome -- Herman Et Al. 79 (5): 743 -- Pedi Hand radiographs in russellsilver syndrome. TE Herman, JD Crawford, RH Clevelandand DC Kushner. Left-hand radiographs were analyzed for bone age of 15 http://pediatrics.aappublications.org/cgi/content/abstract/79/5/743

QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: This Article P Rs: Submit a response Alert me when this article is cited Alert me when P ... Alert me if a correction is posted Services E-mail this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Download to citation manager PubMed PubMed Citation Articles by Herman, T. E. Articles by Kushner, D. C. Hand radiographs in Russell-Silver syndrome TE Herman, JD Crawford, RH Cleveland and DC Kushner Left-hand radiographs were analyzed for bone age of 15 patients with Russell-Silver syndrome. No single finding was pathognomonic. However, in children between 2 and 10 years of age, the concordance of significantly delayed maturation, clinodactyly, fifth middle or distal phalangeal hypoplasia, ivory epiphyses, and a second metacarpal pseudoepiphyses is suggestive and should prompt a search for the well- recognized clinical features of this condition. Volume 79, Issue 5, pp. 743-744, 05/01/1987

62. Database Search Results Searched keywords for russellsilver syndrome. Human Growth Foundation MAGIC Foundation for Children s Growth NHIC Home Page. http://www.health.gov/nhic/NHICScripts/Hitlist.cfm?Keyword=Russell-Silver Syndro

63. Hoeven Signs Bill To Increase Coverage For Those Diagnosed With Russell-Silver S Laikyn Zietz was diagnosed with russellsilver syndrome shortly after birth. russell-silver syndrome is a rare, inherited metabolic disorder that http://www.governor.state.nd.us/media/news-releases/2005/04/050408.html

Current News News Release Archive Trade Missions Governor's Collection of Speeches, Testimonials, Articles and Interviews ... Printer friendly version April 8, 2005 For further information, please Contact the Governor's Office Hoeven Signs Bill To Increase Coverage For Those Diagnosed With Russell-Silver Syndrome BISMARCK, N.D. - Gov. John Hoeven today signed into law Senate Bill 2395 at a bill signing attended by Sens. Judy Lee and Dwight Cook, Reps. RaeAnn Kelsch and Dwight Wrangham, members of the Senate Human Services Committee and the Zietz family. Laikyn Zietz was diagnosed with Russell-Silver Syndrome shortly after birth. SB 2395 was passed by the North Dakota Legislature to provide funding for medical food and growth hormone treatment for those diagnosed with Russell-Silver Syndrome. The bill authorizes the Department of Human Services to provide up to $50,000 per child each biennium to cover prescription and dietary expenses for individuals through the age of 18, regardless of income and at no cost to them. Russell-Silver Syndrome is a rare, inherited metabolic disorder that prevents the body from producing growth hormones. The body is unable to metabolize amino acids essential to building proteins, affecting growth and development.

64. Geneticalliance.org russellsilver syndrome Support Groups. 2 organization(s) found. previous Page1 of 1 next . MAGIC Foundation 6645 West North Avenue Oak Park, IL 60302 http://www.geneticalliance.org/ws_display.asp?filter=support_groups_by_disease&t

65. Russell-Silver Syndrome Children with russellsilver syndrome are born small and generally achieve lessthan 5 feet There is no specific treatment for russell-silver syndrome. http://www.shands.org/health/information/article/001209.htm

Disease Injury Nutrition Poison ... Z Russell-Silver syndrome Definition: 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. Alternative Names: Silver-Russell syndrome; Silver syndrome Causes, incidence, and risk factors: Genetic problems are thought to cause this syndrome, although the specific gene(s) remain to be discovered. The pattern of inheritance has not been determined, but in most cases it seems to occur without any family history of the condition. Children with Russell-Silver syndrome are born small and generally achieve less than 5 feet at adult height. Side-to-side asymmetry is fairly common. For example, a left body part may be larger than the right counterpart. This asymmetry may occur anywhere including the face. Other characteristics include excessive sweating , a small triangular face that makes the skull look large by comparison, inward curving 5th fingers, and colored spots on the skin called cafe-au-lait spots Symptoms: slow growth before birth short stature throughout childhood and at final height cafe-au-lait (coffee with milk) colored spots severe feeding problems in childhood (reflux disease, food aversion, failure to thrive)

66. Trisomy 7 Mosaicism (1997) Molecular studies in 37 silverrussell syndrome patients frequency andetiology of uniparental disomy. Human Genetics 100415-9. PubMed http://www.medgen.ubc.ca/wrobinson/mosaic/trisomy7.htm

chromosomal Mosaicism HOME TABLE OF CONTENTS SEARCH BACKGROUND ... GLOSSARY Chromosome specific Trisomy TRISOMY 7 MOSAICISM Complete trisomy 7 has never been reported in a liveborn child. Trisomy 7 is one of the most common aneuploidies detected on chorionic villus sampling . In general, prenatal detection of trisomy 7 is associated with a good outcome. However maternal UPD 7 is strongly associated with severe growth restriction placenta (CPM) appears to be primarily of mitotic origin, resulting from somatic duplication of chromosome 7. This explains the generally good outcome in the majority of cases. Given the mitotic origin the risk of fetal UPD 7 is low. Kalousek et al (1996) showed that CPM for trisomy 7 with biparental inheritance has no adverse effect on fetal growth. Thus, CVS alone is a poor predictor of pregnancy outcome for trisomy 7. When CVS is combined with DNA studies to reveal the origin of CPM (mitotic or meiotic) and parental origin of the chromosome 7s, a more reliable prediction for pregnancy outcome can be discussed (Kalousek et al, 1996). X Y Monosomy X Triploidy / Tetraploidy Trisomy 7 detected on CVS Sachs et al (1990) reported on 5 cases of trisomy 7 mosaicism. In these cases the percentage of abnormal cells measured on CVS direct studies ranged from 5%-68%. In all 5 cases the pregnancies resulted in a normal outcome.

67. Clinical Dysmorphology - Abstract: Volume 13(2) April 2004 P 95-98 Severe Hemihy russellsilver syndrome is a genetically heterogeneous condition. Her phenotypeactually was quite consistent with russell-silver syndrome. http://www.clindysmorphol.com/pt/re/mcd/abstract.00019605-200404000-00008.htm

LWWOnline LOGIN eALERTS REGISTER ... Archive Severe hemihypotrophy in a female... ARTICLE LINKS: Fulltext PDF (142 K) Permissions Severe hemihypotrophy in a female infant with mosaic Turner syndrome: a variant of Russell-Silver syndrome? Clinical Dysmorphology. 13(2):95-98, April 2004. Li, Chumei C. a b; Chodirker, Bernard N. a b; Dawson, Angelika J. a b c; Chudley, Albert E. a b Abstract: Subscribe to RSS feed utrdc-pt02 Release 4.0

68. Clinical Dysmorphology - UserLogin A diagnosis of russellsilver syndrome was advanced on the basis of growthretardation, russell-silver syndrome. J Med Genet (1988) 25 557-560. http://www.clindysmorphol.com/pt/re/mcd/fulltext.00019605-200104000-00007.htm

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69. Russell-Silver Syndrome russellsilver syndrome is another type of dwarfism, although less common. Sometimes doctors refer to russell-silver syndrome as silver-russell syndrome http://www.buradley.com/rss/rssstory.htm

Russell-Silver Syndrome - A Story I created this article for two distinct purposes. First, I wanted to have a way to inform those who were unaware of Russell-Silver syndrome. Second, and most important, I wanted to create an informative and concise summary of Russell-Silver syndrome for parents with newly born or diagnosed RSS children. I intend this article to an overview of the syndrome. If you want more detailed information on this subject, You can research more on your own. The bibliography located at the end of this manual can get you started on the right track. If, in the course of reading this manual, you run across words you don't know, please refer to the glossary at the end. You may wish to glance over the glossary first is you are unfamiliar with medical terminology related to dwarfism and Russell-Silver syndrome. Defining Russell-Silver Syndrome When the average American thinks of a dwarf, they usually picture a person with a normal sized torso and head, but with shortened limbs, looking like the characters from the movie Willow . This type of dwarfism, known as Acondroplasia, is only one of the nearly 300 diagnosable dwarfisms known to modern medicine. Russell-Silver syndrome is another type of dwarfism, although less common. Both Dr. A. Russell and Dr. H. K. Silver first diagnosed Russell-Silver syndrome (abbreviated RSS) separately in the mid 1960's. The two doctor's findings were later combined to one diagnoses. Sometimes doctors refer to Russell-Silver syndrome as Silver-Russell syndrome. I will get into the differences in these names later.

70. What Is Russell-Silvers Syndrome? As a result, the syndrome received its name. russellsilver syndrome (RSS) isalso known as silver-russell syndrome, silver syndrome, and russell syndrome. http://www.buradley.com/rss/desc.htm

Russell-Silver Syndrome In 1953 and 1954, respectively, Dr. H. K. Silver and Dr. A. Russell independently described a special group of IUGR (Intrauterine Growth Retardation) children with short stature along with a small triangular face, low-set ears, incurved fifth fingers, and other characteristics. Their independent and varied findings were eventually determined to be a variation of the same syndrome. (A syndrome is a group of physical signs and symptoms which make up a specific disease or disorder.) As a result, the syndrome received its name. Russell-Silver Syndrome (RSS) is also known as Silver-Russell Syndrome, Silver Syndrome, and Russell Syndrome. One of the interesting and at the same time unsettling aspects of this syndrome is the very wide variation of its characteristics. Some individuals with RSS have many of the documented traits, while others have very few. Mental retardation is not characteristic of this disorder.

71. Online And Offline Support: R Please note Children, teens, and adults with russellsilver syndrome have specificfacial Association for Children with russell-silver syndrome, Inc. http://www.widesmiles.org/support/r.html

R Robinow Syndrome Robinow Syndrome Foundation People served: Individuals and families dealing with Robinow Syndrome Services provided: Information and support Address: P.O. Box 1072, Anoka MN 55303 Phone number: (763) 434-1152 Email Address: kmkruger@comcast.net Contact person: Karla Kruger Romberg Syndrome/Parry-Romberg Syndrome The Rombergs Connection and The Romberg's Connection Annex People served: Individuals dealing with Rombergs Syndrome Services provided: Information and support Email address: rombergs@hotmail.com Main Website: http://www.geocities.com/HotSprings/1018/ Annex Website: http://www.geocities.com/HotSprings/Spa/4818/ Rubinstein-Taybi Syndrome Please note: Children, teens, and adults with Rubinstein-Taybi Syndrome have specific facial features that do not require reconstructive surgery. Rubinstein-Taybi Parent Group (RTPG) People served: Parents of children with Rubinstein-Taybi Syndrome Services provided: Support, parent-matching, information, and newsletter Address: PO Box 146, Smith Center KS 66967 Phone number: (785) 697-2984 Contact people: Garry and Lorrie Baxter Email address: lbaxter@ruraltel.net

72. GEMdatabase - Selected Title TITLE, russellsilver syndrome. DESCRIPTION, This review focuses on the diagnosis, CONDITIONS, russell-silver syndrome. SUBJECTS. AVAILABILITY http://www.gemdatabase.org/GEMDatabase/TitleDetailsOne.asp?TitleID=993

73. Healthfinder® - Russell-Silver Syndrome Carefully selected government and nonprofit health information on russellSilverSyndrome. http://www.healthfinder.gov/Scripts/SearchContext.asp?topic=760

74. Healthfinder® - Russell-Silver Syndrome Carefully selected government and nonprofit health information on russellSilverSyndrome. http://www.healthfinder.gov/Scripts/SearchContext.asp?topic=760&refine=1

75. Entrez PubMed The silverrussell syndrome (SRS) is characterised by severe intrauterine growthretardation, with a preserved head circumference, leading to a lean body http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=1

76. Entrez PubMed russellsilver syndrome (RSS) is a form of congenital short stature characterizedby severe growth retardation and variable dysmorphic features. http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=1

77. Disease - Russell-Silver Syndrome - Detroit, Michigan Disease russell-silver syndrome - courtesy of Henry Ford Health System ofDetroit, Michigan. http://www.henryfordhealth.org/12233.cfm

3D Tour of the Vattikuti Institute About the Institute The Vattikuti Institute Prostatectomy Prostate Cancer ... Health Encyclopedia Health Encyclopedia Back to main Health Information page Disease - Russell-Silver syndrome Definition: 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. Alternative Names: Silver-Russell syndrome; Silver syndrome Causes And Risk: Genetic problems are thought to cause this syndrome, although the specific gene(s) remain to be discovered. The pattern of inheritance has not been determined, but in most cases it seems to occur without any family history of the condition. Children with Russell-Silver syndrome are born small and generally achieve less than 5 feet at adult height. Side-to-side asymmetry is fairly common. For example, a left body part may be larger than the right counterpart. This asymmetry may occur anywhere including the face. Other characteristics include excessive sweating , a small triangular face that makes the skull look large by comparison, inward curving 5th fingers, and colored spots on the skin called cafe-au-lait spots Symptoms: slow growth before birth short stature throughout childhood and at final height cafe-au-lait (coffee with milk) colored spots severe feeding problems in childhood (reflux disease, food aversion, failure to thrive)

78. Silver-Russell Dwarfism: Information From Answers.com silverrussell dwarfism, also called silver-russell syndrome or russell-silversyndrome is a growth disorder occurring in approximately 1/75000 births. http://www.answers.com/topic/silver-russell-dwarfism

showHide_TellMeAbout2('false'); Business Entertainment Games Health ... More... On this page: Wikipedia Mentioned In Or search: - The Web - Images - News - Blogs - Shopping Silver-Russell dwarfism Wikipedia Silver-Russell dwarfism Silver-Russell dwarfism , also called Silver-Russell syndrome or Russell-Silver syndrome is a growth disorder occurring in approximately 1/75000 births. It is a genetic anomaly, and there are no tests to determine if this is what a child has. Symptoms are (IUGR) combined with some of the following: Often a diagnosis of Small for Gestation Age (SGA) at birth Feeding problems, the baby is uninterested in feeding and takes only small amounts with difficulty. Excessive sweating as a baby, especially at night, and a greyness or pallor of the skin. This may be a symptom of low blood sugar in the blood ( hypoglycemia Triangular shaped face with a small jaw and a pointed chin. The mouth tends to curve down. A blue tinge to the whites of the eyes in younger children Head appears large - the head circumference may be of normal size which means it can appear large in comparison to a small body size. Wide and late closing fontanelle Clinodactyly, the little finger on each hand may be small and curve inwards.

79. %180860 SILVER-RUSSELL SYNDROME; SRS silverrussell syndrome (SRS) was reported independently by silver et al. (1992) observed severe russell-silver syndrome in a girl with translocation http://srs.sanger.ac.uk/srsbin/cgi-bin/wgetz?[omim-ID:180860] -e

80. *601523 GROWTH FACTOR RECEPTOR-BOUND PROTEIN 10; GRB10 However, the role of GRB10 in russellsilver syndrome was cast in doubt by thereports of Hannula et al. (2001), Hitchins et al. (2001), and McCann et al. http://srs.sanger.ac.uk/srsbin/cgi-bin/wgetz?[omim-ID:601523] -e

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