Medicine:Hamanishi Ueba Tsuji syndrome

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Hamanishi Ueba Tsuji syndrome
Other namescongenital aplasia of the extensor muscles of the fingers and thumb associated with generalized polyneuropathy, polyneuropathy hand defect[1]
Autosomal recessive inheritance, pedigree example.png
This syndrome is inherited in an autosomal recessive fashion
SpecialtyMedical genetics
Symptomsmuscle, nerve, and skeletal problems,
Usual onsetbirth
Durationlife-long
CausesGenetic mutation
Risk factorshaving parents with the disease

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,[2] hypohidrosis, muscular dystrophy, minor physical anomalies (such as camptodactyly), and skeletal muscle atrophy,.[3][4][5] This disorder is inherited in an autosomal recessive fashion, and its exact prevalence is unknown, although it is believed to be around 1 in 100,000.[6] No new cases of this syndrome have been reported since 1986.[7]

References