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Greig cephalopolysyndactyly syndrome

Congenital Malformations and Chromosomal Abnormalities

Greig cephalopolysyndactyly syndrome is a genetic disorder that disturbs the development of the limbs, head and face, and its features range from very mild to severe. People with it typically have one or more extra fingers or toes, or an unusually wide thumb or big toe. The skin between the digits may be fused, the eyes may be set widely apart, the head may be abnormally large with a high, prominent forehead, and more rarely seizures and developmental delay occur. It is caused by chromosomal changes affecting the GLI3 gene on chromosome 7, either a large deletion or translocation or a mutation in the gene itself, and it is inherited in an autosomal dominant pattern, though rare cases arise sporadically. Diagnosis is usually presumptive, based on the triad of preaxial polydactyly with syndactyly, macrocephaly and hypertelorism, and management centres on surgery for the limb abnormalities. This entry records descriptions and is not medical advice.

Facts
Classification
ICD-10 Chapter
XVII: Congenital Malformations, Deformations and Chromosomal Abnormalities 1
Communicable or Non-communicable
Non-Communicable 2
Transmission Route
Non-Transmissible 2
Causative Agent
Causative Agent (category)
Genetic / Hereditary 1
Prevalence Band
Rare (Under 1 in 2000) 3
Sources
1. Greig cephalopolysyndactyly syndrome (Wikipedia)
  • Lead paragraph, first sentence
    Greig cephalopolysyndactyly syndrome is a disorder that affects development of the limbs, head, and face.
  • Pathophysiology
    Mutations in the GLI3 gene cause Greig cephalopolysyndactyly syndrome.
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2. MedlinePlus Genetics, National Library of Medicine: Greig cephalopolysyndactyly syndrome
MedlinePlus Genetics, National Library of Medicine
  • Genetics page - communicable-or-non-communicable
    This condition is inherited in an autosomal dominant pattern, which means one altered or missing copy of the GLI3 gene in each cell is sufficient to cause the disorder.
  • Genetics page - transmission-route
    This condition is inherited in an autosomal dominant pattern, which means one altered or missing copy of the GLI3 gene in each cell is sufficient to cause the disorder.
View the Source
3. Orphadata (Orphanet): Orphadata: Epidemiology of rare diseases (en_product9_prev)
Orphadata (Orphanet)ORPHA:380
Quote, ORPHA:380
Prevalence at birth Class only 1-9 / 1 000 000
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