نتایج جستجو برای: dysplasia epiphysealis hemimelica

تعداد نتایج: 28617  

Journal: :Orthopedics 2012
Levent Buluc Ozgur Selek Yasemin Aranay

Acromicric dysplasia is a skeletal dysplasia that is characterized by short stature, short hands and feet, typical facial dysmorphism, normal mental development, and characteristic hand radiology. Carpal tunnel syndrome may be seen in adults with acromicric dysplasia; however, to the authors' knowledge, it has not been reported in pediatric patients. This article describes a 9-year old boy with...

Journal: :razavi international journal of medicine 0
norman ramirez mayaguez medical center, mayaguez, hospital de la concepcion, san german, puerto rico; school of medicine, ponce health sciences university, ponce, puerto rico; mayaguez medical center, mayaguez, hospital de la concepcion, san german, p. o. box: 6847, mayaguez, puerto rico. tel: +1-7872642066 sigfredo villarin school of medicine, ponce health sciences university, ponce, puerto rico robert ritchie ponce research institute, ponce, puerto rico kenira j. thompson department of physiology, neuroscience division, ponce health sciences university, ponce research institute, ponce, puerto rico

conclusions getting a complete knowledge of the condition and evaluating different treatment modalities to treat thoracic insufficiency syndrome. results a direct enlargement of the thorax that will thus provide sufficient space for lung growth; the correction of both the three-dimensional thoracic deformity and the progressive scoliosis. recent findings have revealed that veptr instrumentation...

Heidari, A, Tavana, N,

Introduction: Dentin Dysplasia is one of the rare hereditary diseases that the enamel is normal, but it also affects the dentin and  the shape of the tooth pulp. Due to the low prevalence of this disease, a case of dentin dysplasia with the classical and atypical dentin dysplasia type 1 is presented. Case presentation:A 11-year-old girl with the mobility of lower central teeth that has severe ...

The rare form of skeletal dysplasia is thanatophoric dysplasia. The meaning for thanatophoric dysplasia is death bearing which is derived from Greek word. It occurs 1in 20,000 to 50,000. It is mainly due to mutations in the fibroblast growth factor receptor 3gene. Features of thanatophoric dysplasia are frontal bossing, prominent eyes, narrow thorax, protruded abdomen and bowed legs. The knowle...

Background and objective:Candida albicans (C. albicans) play a significant role in oral mucosal carcinogenesis. It can be identified using various techniques in cytological smears. But, very few studies have been conducted on histopathological sections using calcofluor white M2R under fluorescent microscopy. Additionally, detection and quantification ...

امینی , سیدمحمد, باقری , بابک, داوودی , مهدی, مخبری , وحید,

Background: Renal artery stenosis, which is defined as narrowing of one or both renal arteries or their branches, is one of the most common causes of secondary hypertension. The majority of renal vascular lesions show either fibromuscular dysplasia or atherosclerosis. Fibromuscular dysplasia is a common cause of renovascular hypertension in younger patients, and 90% of patients are young wome...

Alireza Baradaran-Heravi Bita Geramizadeh, Majid Yavarian Mehran Karimi, Mitra Basiratnia,

Schimke immuno-osseous dysplasia is a rare autosomal recessive multisystem disorder characterized by steroid-resistant nephrotic syndrome, immunodeficiency, and spondyloepiphy-seal dysplasia. Mutations in SWI/SNF2 related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1 (SMARCAL1) gene are responsible for the disease. The present report describes, for the f...

Alieh Sadat Javadzadeh Haghighat, Ava Nikbin, Mohammad Talebzadeh, Saeed dashtyari, Seiedeh Tahereh Mohtavipour,

Introdouction: Fibrous dysplasia is a benign fibro-osseous lesion that affects craniofacial bones including the maxilla and mandible. In the most cases of fibrous dysplasia of facial bones, radiographic findings represent lucent or mixed radiolucent-radiopaque lesion with ill-defined borders and gradual blending of its border with adjacent bone . In this presentation, a patient suffering ...

Developmental dysplasia of the hip (DDH) or congenital hip dysplasia (CDH) is the most prevalent developmental childhood hip disorder. It includes a wide spectrum of hip abnormalities ranging from dysplasia to subluxation and complete dislocation of the hip joint. The natural history of neglected DDH in adults is highly variable. The mean age of onset of symptoms is 34.5 years for dysplastic DD...

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