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Other Names for this Disease
- Isolated congenital anosmia
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Congenital anosmia is a very rare condition in which individuals, beginning at birth, have a lifelong inability to smell. Although it can occur alone, it may also be a symptom of another condition such as Kallman syndrome. Congential anosmia in individuals with no other symptoms (isolated congenital anosmia) is thought to be due to errors in the development of the system that enables us to smell (the olfactory system) and may be related to mutations in a gene on chromosome 18. Isolated congenital anosmia is thought to be inherited in an autosomal dominant pattern.
- Ghadami M, et al. Isolated congenital anosmia locus maps to 18p11.23-q12.2. Journal of Medical Genetics. April, 2004. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1735746/pdf/v041p00299.pdf. Accessed March 9, 2011.
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- The The Online Mendelian Inheritance in Man (OMIM) database contains genetics resources that discuss Congenital anosmia. Click on the link to go to OMIM and review these resources.