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High arches
    Differential Diagnosis[Top] [Nav]
familial degenerative neurologic disease (Charcot-Marie-Tooth disease, Freidreich ataxia, hereditary spastic paraplegia, Roussy-Lévy syndrome, myelodysplasia, spina bifida, Refsum disease); relatives of people afflicted as above; isolated familial cases without family history of neurologic disease; pes cavus and lymphedema syndrome
    Discussion -- not available online[Top] [Nav]
    Update Comments[Top] [Nav]
  • Passing mention that pes cavus occurs in Kallmann syndrome. [101]
    Footnotes in Print Edition[Top] [Nav]
    (1) Handbook of Clinical Neurology.
  Vinken PJ, Bruyn GW. Amsterdam: North Holland: 1975;21:263-269.
    (2) "Idiopathic" pes cavus: an investigation into its ætiology.
  Brewerton DA, et al.   Br Med J. 1963;2:659-661.  Medline
    (3) Heritable Disorders of Connective Tissue. 4th ed.
  McKusick VA. St. Louis: Mosby, 1972: 82.
    New References[Top] [Nav]
    101.Brief report: intragenic deletion of the KALIG-1 gene in Kallmann's syndrome [see comments].
  Bick D, Franco B, et al.   N Engl J Med 1992 Jun 25;326(26):1752-5.  Pubmed  Similars
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    ©1986-2000 John Sotos, MD. All rights reserved.  Last updated 16:35 PDT on July 4, 2000.[Top]

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