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Results 1 - 10 of 29 for silver
  1. Russell-Silver syndrome 
    Russell-Silver syndrome is a growth disorder characterized by slow growth before and after birth. Babies with this condition have a low birth weight and often ...
    https://medlineplus.gov/genetics/condition/russell-silver-syndrome - Genetics
  2. Silver syndrome 
    Silver syndrome belongs to a group of genetic disorders known as hereditary spastic paraplegias. These disorders are ... nervous system involved in muscle movement and sensations. Silver syndrome is a complex hereditary spastic paraplegia.The ...
    https://medlineplus.gov/genetics/condition/silver-syndrome - Genetics
  3. H19 gene 
    ... are also responsible for some cases of Russell-Silver syndrome, a disorder characterized by slow growth before ... have the opposite effect on growth.In Russell-Silver syndrome, the paternally inherited copy of the IC1 ...
    https://medlineplus.gov/genetics/gene/h19 - Genetics
  4. BSCL2 gene 
    ... mutations described above, have been reported to cause Silver syndrome. This condition is characterized by muscle weakness ... causes muscle weakness and spasticity in people with Silver syndrome.It is unclear how the same mutations ...
    https://medlineplus.gov/genetics/gene/bscl2 - Genetics
  5. IGF2 gene 
    ... are also responsible for some cases of Russell-Silver syndrome, a disorder characterized by slow growth before ... have the opposite effect on growth.In Russell-Silver syndrome, the paternally inherited copy of the IC1 ...
    https://medlineplus.gov/genetics/gene/igf2 - Genetics
  6. Chromosome 7 
    ... which is described in more detail with Russell-Silver syndrome, below). It remains unclear how having two ... as part of a larger condition called Russell-Silver syndrome (described below). More About This Health Condition ...
    https://medlineplus.gov/genetics/chromosome/7 - Genetics
  7. Chromosome 11 
    ... Condition Like Beckwith-Wiedemann syndrome (described above), Russell-Silver syndrome can result from changes in genes in the 11p15.5 region. Specifically, Russell-Silver syndrome has been associated with changes in genomic ...
    https://medlineplus.gov/genetics/chromosome/11 - Genetics
  8. Asparagine synthetase deficiency 
    ... Levi D, Lev D, Lerman-Sagie T, Leshinsky-Silver E, Anikster Y, Ben-Asher E, Olender T, ... Banwell B, Joshi RB, He XP, Patry L, Silver RJ, Dobrzeniecka S, Islam MS, Hasnat A, Samuels ...
    https://medlineplus.gov/.../asparagine-synthetase-deficiency - Genetics
  9. FOXP2-related speech and language disorder 
    ... as part of a larger condition called Russell-Silver syndrome. In addition to speech and language problems, ... UPD of chromosome 7 as part of Russell-Silver syndrome, the condition is not inherited. UPD occurs ...
    https://medlineplus.gov/...oxp2-related-speech-and-language-disorder - Genetics
  10. Alternating hemiplegia of childhood 
    ... Murphy KJ, Shianna KV, Gumbs CE, Little L, Silver K, Ptacek LJ, Haan J, Ferrari MD, Bye ... 2012 Jul 30. Citation on PubMed Sweney MT, Silver K, Gerard-Blanluet M, Pedespan JM, Renault F, ...
    https://medlineplus.gov/.../alternating-hemiplegia-of-childhood - Genetics
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