نتایج جستجو برای: twenty nail dystrophy

تعداد نتایج: 146313  

Alireza Hootkani, E. Ghayyem Hasankhani M.R. Fayyazi Bordbar

Background: There is inconsistent information about the role of psychological factors in the incidence of reflex sympathetic dystrophy (RSD) in patients with distal radius fractures. The present study was thus undertaken to evaluate the relationship between some of these factors and the occurrence of reflex sympathetic dystrophy in patients with distal radius fracture. Methods: One hundred and ...

Journal: :Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 2014
Anurag N Malani Lisa Kerr Janet Obear Bonita Singal Carol A Kauffman

BACKGROUND Voriconazole was 1 of 2 antifungal agents recommended for treatment of fungal infections associated with injection of contaminated methylprednisolone. Alopecia and nail changes are not commonly reported side effects of voriconazole. Having noted increasing hair loss among our patients treated with voriconazole, we sought to determine the prevalence and characteristics of alopecia ass...

2013
A Wilharm I Marintschev G O Hofmann F Gras

BACKGROUND Intramedullary nailing is a standard surgical procedure for fixation of proximal femoral fractures, but is associated with considerable radiation exposure for controlling the implant placement, due to the percutaneous insertion technique.The aim of this study was the evaluation of potential benefits of 2D-fluoroscopic based navigation focused on the reduction of radiation exposure, a...

Journal: :The Journal of bone and joint surgery. American volume 2013
Alexander Van Tongel Ehud Atoun Ali Narvani Giuseppe Sforza Stephen Copeland Ofer Levy

BACKGROUND Shoulder girdle muscle weakness is the most constant feature of facioscapulohumeral muscular dystrophy and leads to scapular winging. Mechanical fixation of the scapula to the thoracic wall provides a stable fulcrum on which the deltoid muscle can exert its action on the humerus. The aim of this study was to evaluate the medium to long-term outcome of thoracoscapular arthrodesis with...

Journal: :The Journal of bone and joint surgery. British volume 1978
S A Copeland R C Howard

Eleven thoracoscapular fusion operations have been done on six patients. The indication is symptomatic winging of the scapula caused by thoracoscapular muscle paresis with intact function in the deltoid. This situation almost exclusively occurs in facioscapulohumeral dystrophy. The operation is successful in achieving stability of the scapula and in greatly improving function and cosmesis. Alth...

2017
Zoya R. Umakhanova Sergei N. Bardakov Mikhail O. Mavlikeev Olga N. Chernova Raisat M. Magomedova Patimat G. Akhmedova Ivan A. Yakovlev Gimat D. Dalgatov Valerii P. Fedotov Artur A. Isaev Roman V. Deev

To date, over 30 genes with mutations causing limb-girdle muscle dystrophy have been described. Dysferlinopathies are a form of limb-girdle muscle dystrophy type 2B with an incidence ranging from 1:1,300 to 1:200,000 in different populations. In 1996, Dr. S. N. Illarioshkin described a family from the Botlikhsky district of Dagestan, where limb-girdle muscle dystrophy type 2B and Miyoshi myopat...

A Nasiri A Zamanian K Nabizadeh

Background: The nails of hands and feet are involved in the course of many dermatoses and some systemic diseases. They may have diagnostic or prognostic value in some diseases. Objective: The aim of this study was to evaluate nail lesions in patients referred to Dermatology Department of Sina Hospital in Hamadan from April 1999 to April 2000. Patients and Methods: This cross-sectional des...

Journal: :Biomedical Research and Therapy 2021

Background: Pachyonychia congenita (PC) comprises a group of rare autosomal dominant genetic disorders. It is characterized by hypertrophic nail dystrophy, focal palmoplantar keratoderma, follicular keratosis, and oral leukokeratosis. associated with mutations in five differentiationspecific keratin genes: KRT6A, KRT6B, KRT6C, KRT16, or KRT17. The case being reported for its rarity. To the best...

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