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Acroosteolysis (Jackey syndrome): analysis of clinical observation
Author(s) -
А. П. Чернов,
Aleksandr S. Pankratov,
Denis A. Ogurtsov
Publication year - 2022
Publication title -
vestnik travmatologii i ortopedii imeni n.n. priorova
Language(s) - English
Resource type - Journals
eISSN - 2658-6738
pISSN - 0869-8678
DOI - 10.17816/vto99825
Subject(s) - medicine , dermatology , disease , pathology
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].

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