Zobrazeno 1 - 10
of 203
pro vyhledávání: '"Sprengel's Deformity"'
Autor:
Dhekra Ismail, Lilia Kraoua, Sylvie Jaillard, Hela Bellil, Mohamed Zairi, Faouzi Maazoul, Ridha Mrad, Mohamed Nabil Nessib, Mediha Trabelsi
Publikováno v:
Molecular Cytogenetics, Vol 17, Iss 1, Pp 1-9 (2024)
Abstract Background Interstitial chromosome 11 long arm deletions (11q13-q23) represent a rare cytogenetic abnormality characterized by non-specific clinical features including intellectual disability and several malformations without a clear genotyp
Externí odkaz:
https://doaj.org/article/0ce03cf3ee914d5480ebaf5acbd4d46f
Autor:
Khadija Laasri, Zineb Izi, Yahya El harras, Salma Marrakchi, Fatima Zahra Laamrani, Laila Jroundi, Omar El aoufir
Publikováno v:
Radiology Case Reports, Vol 20, Iss 1, Pp 133-135 (2025)
The features of Sprengel's deformity, also known as congenital high scapula, include abnormal positioning and dysplasia of the affected scapula, with a possible omovertebral connection or atrophy of the surrounding muscles. This case primarily aims t
Externí odkaz:
https://doaj.org/article/a6914aa5df4746b79aac65f784bdad0d
Publikováno v:
Journal of Medical Case Reports, Vol 18, Iss 1, Pp 1-5 (2024)
Abstract Background Sprengel’s deformity is a congenital abnormality of the shoulder girdle. Because scapular retraction, such as the Green procedure, is usually performed during childhood to improve esthetics and shoulder function, Sprengel’s de
Externí odkaz:
https://doaj.org/article/49afbb1be963458eb183abafb9cdb0a5
Akademický článek
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Autor:
Sergey O. Ryabykh, Dmitry M. Savin, Marat S. Sayfutdinov, Polina V. Ochirova, Alexander V. Gubin, Egor Yu. Filatov, Gleb E. Ulrikh, Alexander A. Skripnikov
Publikováno v:
Гений oртопедии, Vol 25, Iss 4, Pp 550-554 (2019)
Design Presentation of clinical cases and literature analysis. Material and methods Clinical observation of patients with congenital cervical spine and shoulder girdle anomalies operated on with neuromonitoring was performed. Operative treatment of
Externí odkaz:
https://doaj.org/article/152effce88d24d3a9773d09d4f2b4dd3
Autor:
Shuai Guo, Xue-Feng Fan, Jie-Yuan Jin, Liang-Liang Fan, Lei Zeng, Zheng-Bing Zhou, Rong Xiang, Ju-Yu Tang
Publikováno v:
Molecular Cytogenetics, Vol 11, Iss 1, Pp 1-6 (2018)
Abstract Background Chiari malformation type II (CM-II) is mainly characterized by elongation and descent of the cerebellum through the foramen magnum into the spinal canal. Moreover, CM-II is uniquely associated with myelomeningocele. Sprengel’s d
Externí odkaz:
https://doaj.org/article/26c21bbdbdb5424eb7a0c9638e9dbd95
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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Publikováno v:
Clinical Imaging. 78:45-50
We present a case of Klippel-Feil Syndrome, a congenital skeletal defect where multiple cervical vertebral bodies are fused. Klippel-Feil Syndrome has multiple associated anomalies, with a notable one being Sprengel's deformity. In this case, the pat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c72900a557c790cf1278e5785e6cc6ad
https://doi.org/10.1016/j.clinimag.2021.02.041
https://doi.org/10.1016/j.clinimag.2021.02.041
Publikováno v:
SN Comprehensive Clinical Medicine. 3:754-758
Sprengel’s deformity is a congenital anomaly characterized by a hypoplastic and elevated scapula that results in cosmetic and functional impairment. In this study, we report the results of 3 severe cases of bilateral Sprengel’s deformity with ass
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::11253d03d76d6ea7384fe4d588fca3f9
https://doi.org/10.1007/s42399-021-00781-y
https://doi.org/10.1007/s42399-021-00781-y
Publikováno v:
Journal of Shoulder and Elbow Surgery. 30:e1-e9
Sprengel's deformity is a congenital anomaly of the scapula and can be associated with reduced shoulder mobility and esthetic concerns. Controversies remain regarding its natural history, radiographic findings, and optimal treatment strategy.A total
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a632accabde13c9e5b76892673bd422
https://doi.org/10.1016/j.jse.2020.04.018
https://doi.org/10.1016/j.jse.2020.04.018