About: Hamanishi Ueba Tsuji syndrome     Goto   Sponge   NotDistinct   Permalink

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Hamanishi Ueba Tsuji syndrome is a rare genetic motor and sensorial neuropathy which is characterized by digital (thumb and fingers) flexion malformations, reduced touch and pain sensations of the limbs, hypohidrosis, muscular distrophy, minor physical anomalies (such as camptodactyly), and skeletal muscle atrophy,. This disorder is inherited in an autosomal recessive fashion, and it's exact prevalence is unknown, although it is believed to be around 1 in 100,000. No new cases of this syndrome have been reported since 1986.

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  • Hamanishi Ueba Tsuji syndrome (en)
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  • Hamanishi Ueba Tsuji syndrome is a rare genetic motor and sensorial neuropathy which is characterized by digital (thumb and fingers) flexion malformations, reduced touch and pain sensations of the limbs, hypohidrosis, muscular distrophy, minor physical anomalies (such as camptodactyly), and skeletal muscle atrophy,. This disorder is inherited in an autosomal recessive fashion, and it's exact prevalence is unknown, although it is believed to be around 1 in 100,000. No new cases of this syndrome have been reported since 1986. (en)
name
  • Hamanishi Ueba Tsuji syndrome (en)
foaf:depiction
  • http://commons.wikimedia.org/wiki/Special:FilePath/Autosomal_recessive_inheritance,_pedigree_example.png
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onset
  • birth (en)
symptoms
  • muscle, nerve, and skeletal problems, (en)
caption
  • This syndrome is inherited in an autosomal recessive fashion (en)
causes
duration
  • life-long (en)
synonyms
  • congenital aplasia of the extensor muscles of the fingers and thumb associated with generalized polyneuropathy, polyneuropathy hand defect (en)
has abstract
  • Hamanishi Ueba Tsuji syndrome is a rare genetic motor and sensorial neuropathy which is characterized by digital (thumb and fingers) flexion malformations, reduced touch and pain sensations of the limbs, hypohidrosis, muscular distrophy, minor physical anomalies (such as camptodactyly), and skeletal muscle atrophy,. This disorder is inherited in an autosomal recessive fashion, and it's exact prevalence is unknown, although it is believed to be around 1 in 100,000. No new cases of this syndrome have been reported since 1986. (en)
risks
  • having parents with the disease (en)
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alias
  • (en)
  • congenital aplasia of the extensor muscles of the fingers and thumb associated with generalized polyneuropathy, polyneuropathy hand defect (en)
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