The pachydermoperiostosis: Reeducation care about 2 cases
نویسندگان
چکیده
منابع مشابه
Primary Pachydermoperiostosis and report of two cases in a family
Pachydermoperiostosis (PDP) is a rare hereditary disease characterized by folded coarse skin, hyperostosis, clubbing of fingers and abnormalities in other organs such as gastrointestinal tract. Because of safety parents guides us to familial incidence and penetration of gene in 50% of cases. Diagnosis is based on clinical and radiological findings. Males are more susceptible than females to thi...
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Pyoderma gangrenosum occurrence in a familial pattern is extremely rare. We report pyoderma gangrenosum in two Tunisian siblings with onset respectively at 28 and 26 years old. The initial lesion was a pustule that breaks down to form an ulcer with an erythematous border. Treatment with oral corticosteroids induced an excellent clinical response. This familial clustering suggests a possible gen...
متن کاملClinical Policy Title: Neuromuscular reeducation
ABOUT THIS POLICY: Select Health of South Carolina has developed clinical policies to assist with making coverage determinations. Select Health of South Carolina’s clinical policies are based on guidelines from established industry sources, such as the Centers for Medicare & Medicaid Services (CMS), state regulatory agencies, the American Medical Association (AMA), medical specialty professiona...
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The authors report 2 cases of divergent fracture-dislocation of the ankle. They remind diagnostic problems and show the ease of diagnosis. The literature review confirms that this is a rare lesion. Pathological stages are now well codified. After reduction, the evolution is favourable rule. A year back, the results are satisfactory and 2 patients had no pain, with resumption of their daily acti...
متن کامل[Pachydermoperiostosis (idiopathic hypertrophic osteoarthropathy)].
Introduction Pachydermoperiostosis is a syndrome characterized by finger clubbing, periosteal new bone formation especially over the distal ends of long bones, and coarsening of the facial features, with thickening, furrowing and oiliness of the skin of the face and forehead. The first reported cases were the Hagner brothers, who had typical features of this syndrome. They were first described ...
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ژورنال
عنوان ژورنال: Annals of Physical and Rehabilitation Medicine
سال: 2014
ISSN: 1877-0657
DOI: 10.1016/j.rehab.2014.03.706