About: Feigenbaum-Bergeron-Richardson syndrome     Goto   Sponge   NotDistinct   Permalink

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Feigenbaum Bergeron Richardson syndrome, also known as Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome is a very rare fatal genetic disorder which is characterized by atherosclerosis, hearing loss, diabetes mellitus, epilepsy, progressive neurological deterioration and nephropathy. This disorder has been described in two brothers, and is it thought to be inherited in either an atosomal or X-linked recessive manner. No new cases have been reported since 1994. People with this disorder don't usually live beyond 30 to 40 years of age.

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  • Feigenbaum-Bergeron-Richardson syndrome (en)
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  • Feigenbaum Bergeron Richardson syndrome, also known as Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome is a very rare fatal genetic disorder which is characterized by atherosclerosis, hearing loss, diabetes mellitus, epilepsy, progressive neurological deterioration and nephropathy. This disorder has been described in two brothers, and is it thought to be inherited in either an atosomal or X-linked recessive manner. No new cases have been reported since 1994. People with this disorder don't usually live beyond 30 to 40 years of age. (en)
name
  • Feigenbaum-Bergeron-Richardson syndrome (en)
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  • http://commons.wikimedia.org/wiki/Special:FilePath/Feigenbaum-Bergeron-Richardson_syndrome.png
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causes
frequency
  • very rare, only 1 family is known to have the disorder (en)
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  • Atherosclerosis, premature, with deafness, nephropathy, diabetes mellitus, photomyoclonus, and degenerative neurologic disease, premature atherosclerosis with photomyoclonic epilepsy, deafness, diabetes mellitus, nephropathy, and neurodegenerative disorder. (en)
has abstract
  • Feigenbaum Bergeron Richardson syndrome, also known as Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome is a very rare fatal genetic disorder which is characterized by atherosclerosis, hearing loss, diabetes mellitus, epilepsy, progressive neurological deterioration and nephropathy. This disorder has been described in two brothers, and is it thought to be inherited in either an atosomal or X-linked recessive manner. No new cases have been reported since 1994. People with this disorder don't usually live beyond 30 to 40 years of age. (en)
prevention
  • none (en)
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  • (en)
  • Atherosclerosis, premature, with deafness, nephropathy, diabetes mellitus, photomyoclonus, and degenerative neurologic disease, premature atherosclerosis with photomyoclonic epilepsy, deafness, diabetes mellitus, nephropathy, and neurodegenerative disorder. (en)
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