Something To Shoulder: A Case Of Abnormal Shoulder Range Of Motion In An Adolescent

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Something To Shoulder: A Case Of Abnormal Shoulder Range Of Motion In An Adolescent - Page #3

Lab Studies: Creatinine phosphokinase elevated to 561 and genetic testing positive for 4q35 deletion consistent with facioscapulohumeral dystrophy (FSHD) type 1. Other Studies: X-ray of the thoracic spine demonstrated maintained thoracic kyphosis, vertebral body heights, and disc spaces without any fractures or dislocations. <br> <br>X-ray of the right shoulder was remarkable for rotation of the right scapula, but otherwise no fractures or dislocations. The glenohumeral and acromioclavicular joint spaces are maintained. <br> <br>EMG was ordered. However, Neurology recommended deferring it and for the patient to undergo genetic testing, as it would be the most definitive. Consultations: Sports Medicine, Neurology, and Genetics Click here to continue. Challenge yourself by writing down a revised, working diagnosis before moving to the next slide.		Back
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