Acroosteolysis (Jackey syndrome): analysis of clinical observation

A. P. Chernov; A. S. Pankratov; D. A. Ogurtsov

doi:10.17816/vto99825

N.N. Priorov Journal of Traumatology and Orthopedics ›› 2002, Vol. 9 ›› Issue (2) : 85 -86. DOI: 10.17816/vto99825

Short communications

other

Acroosteolysis (Jackey syndrome): analysis of clinical observation

Author information +

History +

PDF

Abstract

Acroosteolysis is a rare congenital disease of the musculoskeletal system, first described by Harnasch in 1950. The disease is hereditary. Sporadic cases of the disease are sometimes observed. Men are affected 2-3 times more often than women [1].

Keywords

acroosteolysis / complete resorption of bone tissue / middle sections of the distal phalanges of the toes

Cite this article

Download citation ▾

A. P. Chernov, A. S. Pankratov, D. A. Ogurtsov. Acroosteolysis (Jackey syndrome): analysis of clinical observation. N.N. Priorov Journal of Traumatology and Orthopedics, 2002, 9(2): 85-86 DOI:10.17816/vto99825

登录浏览全文

4963

注册一个新账户忘记密码

References

Publishing order | Descend order by publishing year | Descend order by cited within

[1]	Рейнберг С.А. Рентгенодиагностика заболеваний костей и суставов. — М., 1964. — Книга 1. — С. 461-463.

[2]	Романовский В.Е. Диагностический справочник клинических синдромов. — Ростов-на-Дону, 1997. — С. 134