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MeSH Tree Location(s) for Angelman Syndrome

Scope Note:
A syndrome characterized by multiple abnormalities, MENTAL RETARDATION, and movement disorders. Present usually are skull and other abnormalities, frequent infantile spasms (SPASMS, INFANTILE); easily provoked and prolonged paroxysms of laughter (hence "happy"); jerky puppetlike movements (hence "puppet"); continuous tongue protrusion; motor retardation; ATAXIA; MUSCLE HYPOTONIA; and a peculiar facies. It is associated with maternal deletions of chromosome 15q11-13 and other genetic abnormalities. (From Am J Med Genet 1998 Dec 4;80(4):385-90; Hum Mol Genet 1999 Jan;8(1):129-35)

Förklaring:
Ett syndrom kännetecknat av ett flertal abnormaliteter, mental efterblivenhet och rörelserubbningar. Det sammanhänger med defekter i kromosom 15q11-13.

See also: Intellectual Disability



Location corresponding to Mesh Number C10.228.662.075

Movement Disorders  Rörelserubbningar
Angelman Syndrome   Angelmans syndrom

Location corresponding to Mesh Number C16.131.077.095

Abnormalities, Multiple  Missbildningar, multipla
Angelman Syndrome   Angelmans syndrom

Location corresponding to Mesh Number C16.131.260.040

Chromosome Disorders  Kromosomrubbningar
Angelman Syndrome   Angelmans syndrom

Location corresponding to Mesh Number C16.320.180.040

Chromosome Disorders  Kromosomrubbningar
Angelman Syndrome   Angelmans syndrom

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© Karolinska Institutet University Library 1998. Last modified 2013-01-31.