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*  Primordial dwarfism - Wikipedia
Silver-Russell dwarfism (Russell-Silver Syndrome). 180860. The final height of those with Russell-Silver syndrome often exceeds ... Like Russell-Silver syndrome, they usually exceed the height of those with Seckel syndrome and ODPDI and II. It is also known ... Some phenotypes (characteristics) of people who have Russell-Silver syndrome are inadequate catch-up growth in first 2 years, ... except in the case of Russell-Silver syndrome (RSS). Individuals with RSS respond favorably to growth hormone treatment. ...
https://en.wikipedia.org/wiki/Primordial_dwarfism
*  Molecular diagnostics - Wikipedia
... such as Silver-Russell syndrome. Molecular diagnostics are used to identify infectious diseases such as chlamydia, influenza ... "Epigenetic and genetic diagnosis of Silver-Russell syndrome". Expert Review of Molecular Diagnostics. 12 (5): 459-471. doi: ... For example, Lynch syndrome is a genetic disease that predisposes patients to colorectal and other cancers; early detection can ... Advances in molecular biology have helped show that some syndromes that were previously classed as a single disease are ...
https://en.wikipedia.org/wiki/Molecular_diagnostics
*  GRB10 - Wikipedia
Ramírez-Dueñas ML, Medina C, Ocampo-Campos R, Rivera H (1992). "Severe Silver-Russell syndrome and translocation (17;20) (q25; ... 1993). "Second observation of Silver-Russel syndrome in a carrier of a reciprocal translocation with one breakpoint at site ...
https://en.wikipedia.org/wiki/GRB10
*  MPLKIP - Wikipedia
"Molecular genetic studies of human chromosome 7 in Russell-Silver syndrome". Genomics. 79 (2): 186-96. doi:10.1006/geno. ...
https://en.wikipedia.org/wiki/MPLKIP
*  C12orf66 - Wikipedia
"Chromosomal rearrangements in patients with clinical features of Silver-Russell syndrome". American Journal of Medical Genetics ... "The 12q14 microdeletion syndrome: six new cases confirming the role of HMGA2 in growth". European Journal of Human Genetics. 19 ... "Refinement of the 12q14 microdeletion syndrome: primordial dwarfism and developmental delay with or without osteopoikilosis". ...
https://en.wikipedia.org/wiki/C12orf66
*  MESTIT1 (gene) - Wikipedia
MESTIT1 is unlikely to cause Russell-Silver syndrome as there is a lack of mutations in this gene in Russell-Silver syndrome ... 1998). "Evidence against a major role of PEG1/MEST in Silver-Russell syndrome". Eur J Hum Genet. 6 (2): 114-20. doi:10.1038/sj. ... 2001). "No evidence of PEG1/MEST gene mutations in Silver-Russell syndrome patients". Am J Med Genet. 104 (3): 225-31. doi: ... Meyer E, Wollmann HA, Eggermann T (2003). "Searching for genomic variants in the MESTIT1 transcript in Silver-Russell syndrome ...
https://en.wikipedia.org/wiki/MESTIT1_(gene)
*  MEST (gene) - Wikipedia
1998). "Evidence against a major role of PEG1/MEST in Silver-Russell syndrome". Eur. J. Hum. Genet. 6 (2): 114-20. doi:10.1038/ ... 2002). "No evidence of PEG1/MEST gene mutations in Silver-Russell syndrome patients". Am. J. Med. Genet. 104 (3): 225-31. doi: ... 2000). "Maternal chromosome 7 hetero/isodisomy in Silver-Russell syndrome and PEG1 biallelic expression". Clin. Dysmorphol. 9 ( ...
https://en.wikipedia.org/wiki/MEST_(gene)
*  ZFP57 - Wikipedia
"Screening for genomic variants in ZFP57 in Silver-Russell syndrome patients with 11p15 epimutations". Eur J Med Genet. 52 (6): ...
https://en.wikipedia.org/wiki/ZFP57
*  IGF2BP3 - Wikipedia
2002). "Characterisation of the growth regulating gene IMP3, a candidate for Silver-Russell syndrome". J. Med. Genet. 39 (8): ...
https://en.wikipedia.org/wiki/IGF2BP3
*  Hemihypertrophy - Wikipedia
Hemihyperplasia is seen in several congenital syndromes including Beckwith-Wiedemann syndrome and Russell-Silver syndrome. ... acmg.net Silver, H. K.; Kiyasu, W; George, J; Deamer, W. C. (1953). "Syndrome of congenital hemihypertrophy, shortness of ... Some of the other syndromes associated with hemihyperplasia may also follow this tumor surveillance protocol. The recommended ... a tumor screening protocol that is recommended for all children with isolated hemihyperplasia and Beckwith-Wiedemann Syndrome. ...
https://en.wikipedia.org/wiki/Hemihypertrophy
*  Epigenetics of human development - Wikipedia
Russell-Silver Syndrome, caused by abnormal lack of methylation in the paternal ICE region, causing Igf2 repression. Symptoms ... "Russel Silver Syndrome." Genetics Home Reference. US National Library of Medicine, Apr. 2008. Web. 09 May 2015. "Prader Willi ... ICF syndrome, caused by a mutation in the DNA methyltransferase 3b gene or DNA hypomethylation, which causes lack of DNA ... Prader-Willi Syndrome, caused by missing paternal expression of the region which UBE3A expression inhibits. Symptoms include ...
https://en.wikipedia.org/wiki/Epigenetics_of_human_development
*  Hirschsprung's disease - Wikipedia
... maternal uniparental heterodisomy 7 and Hirschsprung's disease in a child with Silver-Russell syndrome". European Journal of ... Bardet-Biedl syndrome, Waardenburg-Shah syndrome, Mowat-Wilson syndrome, Goldberg-Shprintzen megacolon syndrome, cartilage-hair ... Bardet-Biedl syndrome Cartilage-hair hypoplasia Congenital central hypoventilation syndrome MEN2 Mowat-Wilson syndrome Smith- ... Lemli-Opitz syndrome Trisomy 21 (Down syndrome) Waardenburg syndrome During normal prenatal development, cells from the neural ...
https://en.wikipedia.org/wiki/Hirschsprung's_disease
*  Insulated neighborhood - Wikipedia
"Disruption of genomic neighbourhood at the imprinted IGF2-H19 locus in Beckwith-Wiedemann syndrome and Silver-Russell syndrome ... or Silver-Russell syndrome (when both alleles have the maternal type of insulated neighborhood). Insulated neighborhoods aid in ... at an imprinted CTCF-binding site near IGF2/H19 form aberrant Insulated Neighborhoods and develop Beckwith-Wiedemann syndrome ( ...
https://en.wikipedia.org/wiki/Insulated_neighborhood
*  Combined bisulfite restriction analysis - Wikipedia
2009). "Diagnosis of Russell-Silver syndrome by the combined bisulfite restriction analysis-denaturing high-performance liquid ... denaturing high performance liquid chromatography in the diagnosis of the genetic imprinting disorder Russell-Silver syndrome ... syndrome, and characterizing DNA methylation patterns in the genome during development in mammals". European Journal of Human ...
https://en.wikipedia.org/wiki/Combined_bisulfite_restriction_analysis
*  Triangular face - Wikipedia
... but has also been described in Russell-Silver syndrome and Turner syndrome. Page 82 in: Elizabeth D Agabegi; Agabegi, Steven S ...
https://en.wikipedia.org/wiki/Triangular_face
*  Chromosome 7 (human) - Wikipedia
Pendred syndrome Romano-Ward syndrome[citation needed] Shwachman-Diamond syndrome Schizophrenia[citation needed] Silver-Russell ... Eggermann T, Begemann M, Binder G, Spengler S (2010). "Silver-Russell syndrome: genetic basis and molecular genetic testing". ... Ehlers-Danlos syndrome hemochromatosis, type 3 Hereditary nonpolyposis colorectal cancer HNPCC4 Lissencephaly syndrome, norman- ... mucopolysaccharidosis type VII or Sly syndrome Muscular dystrophy, limb-girdle, type 1D myelodysplastic syndrome Myotonia ...
https://en.wikipedia.org/wiki/Chromosome_7_(human)
*  CPA5 - Wikipedia
... an imprinted candidate for Silver-Russell syndrome". J. Med. Genet. 40 (4): 249-56. doi:10.1136/jmg.40.4.249. PMC 1735416 . ...
https://en.wikipedia.org/wiki/CPA5
*  H19 (gene) - Wikipedia
... as well as Silver-Russell syndrome. The H19 gene contains 3 Sp1 binding sites, however these 3 sites are present in a part of ... H19 is also known as BWS because aberrant H19 expression can be involved in Beckwith-Wiedemann Syndrome ("BWS"), ...
https://en.wikipedia.org/wiki/H19_(gene)
*  Henry Silver - Wikipedia
Another growth disorder, Russell-Silver syndrome, is named in part after him. He was the co-author of a 1990 study which ... "Silver-Russell Syndrome". Swedish Information Centre for Rare Diseases. Retrieved May 11, 2013. "The High Cost of Doctoring". ... In 1957, Silver joined the University of Colorado School of Medicine. From 1978 to his death, Silver served as the medical ... Henry Silver was born in Philadelphia in 1918. He attended medical school at the University of California at Berkeley. Silver ...
https://en.wikipedia.org/wiki/Henry_Silver
*  Seipin - Wikipedia
Common Therapies in Lipodystrophy Treatment Silver-Russell syndrome Endoplasmic Reticulum Stress in Beta Cells Muscle Weakness ... Additionally, mutations of BSCL2 have been recently linked to the Silver-Syndrome and Celia's Encephalopathy. The seipin gene ... Silver syndrome and autosomal-dominant distal hereditary motor neuropathy type V. CGL (congenital generalized lipodystrophy) is ... "BSCL2 N88S mutation in A Portuguese patient with the Silver syndrome". Muscle & Nerve. 51 (3): 456-458. doi:10.1002/mus.24455. ...
https://en.wikipedia.org/wiki/Seipin
*  Silver-Russell syndrome - Wikipedia
Silver-Russell syndrome (SRS), also called Silver-Russell dwarfism or Russell-Silver syndrome (RSS) is a growth disorder ... In the United States it is usually referred to as Russell-Silver syndrome, and Silver-Russell syndrome elsewhere. It is one of ... Angelman syndrome, and Beckwith-Wiedemann syndrome), Silver-Russell syndrome may be associated with the use of assisted ... "Silver-Russell Syndrome; SRS". OMIM.. *^ Butler, M. G. (2009). "Genomic imprinting disorders in humans: A mini-review". Journal ...
https://en.wikipedia.org/wiki/Russell-Silver_syndrome
*  RSS (disambiguation) - Wikipedia
Russell-Silver syndrome Recombination signal sequences, genes used to generate antibodies and T-cell receptors in immunology ...
https://en.wikipedia.org/wiki/RSS_(disambiguation)
*  Microdontia - Wikipedia
... syndrome Focal dermal hypoplasia Silver-Russell syndrome Williams syndrome Gorlin-Chaudhry-Moss syndrome Coffin-Siris syndrome ... Congenital hypopituitarism Ectodermal dysplasia Down syndrome Ionizing radiation to the jaws during tooth development ( ... neuroectodermal and dermo-odontodysplasia syndromes. Unerupted microdonts may require surgical removal to prevent the formation ... odontogenesis) Chemotherapy during tooth development Marshall syndrome Rieger ...
https://en.wikipedia.org/wiki/Microdontia
*  MAGIC Foundation - Wikipedia
McCune-Albright Syndrome, Russell-Silver Syndrome (also known as Silver-Russell Syndrome), Optic Nerve Hypoplasia, Septo Optic ... McCune-Albright syndrome, Turner syndrome, Russell-Silver syndrome, thyroid disorders (both congenital and acquired), optic ...
https://en.wikipedia.org/wiki/MAGIC_Foundation
*  Leschke syndrome - Wikipedia
Silver-Russell syndrome List of cutaneous conditions Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). ... Leschke syndrome is a condition characterized by growth retardation and intellectual disability. The syndrome is named after ...
https://en.wikipedia.org/wiki/Leschke_syndrome