Structured Summary
Abstract
Genetically and clinically heterogeneous disorder characterized by low birth weight, postnatal growth retardation, facial dysmorphism, bilateral body asymmetry, and clinodactyly of the fifth fingers. Alterations in GENETIC IMPRINTING are involved. Hypomethylation of IGF2/H19 locus near an imprinting center region of chromosome 11p15 plays a role in a subset of Silver-Russell syndrome. Hypermethylation of the same chromosomal region, on the other hand, can cause BECKWITH-WIEDEMANN SYNDROME. Maternal UNIPARENTAL DISOMY for chromosome 7 is known to play a role in its etiology.
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Synonyms
12 entry terms
- Russell Silver Syndrome
- Russell-Silver Syndrome
- Silver Russell Dwarfism
- Silver-Russell Dwarfism
- Dwarfism, Silver Russell
- Dwarfism, Silver-Russell
- Russell-Silver Syndromes
- Silver Russell Syndrome
- Syndrome, Russell Silver
- Syndrome, Russell-Silver
- Syndrome, Silver-Russell
- Syndromes, Russell-Silver
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Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
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History Note
2010
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Previous Indexing
- Growth Disorders (1970-2009)
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AMA Style
References
- National Library of Medicine. Silver-Russell Syndrome. Medical Subject Headings (MeSH). 2026. Unique ID D056730. http://id.nlm.nih.gov/mesh/2026/D056730
- Silver-Russell Syndrome. In: Wikipedia. https://en.wikipedia.org/wiki/Silver%E2%80%93Russell_syndrome
- Silver-Russell Syndrome. In: Wikidata. https://www.wikidata.org/wiki/Q2142496