نتایج جستجو برای: spondylothoracic dysplasia

تعداد نتایج: 28629  

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...

Background & objective: Changes in submucosal vascularization and inflammation, determined by immunohistochemistry staining, were shown to be correlated with the development of dysplasia and invasiveness of epithelial cells in premalignant and malignant lesions. This study evaluated changes in sections routinely stained with Hematoxylin and Eosin (H&E;) in orde...

Journal: :iranian journal of child neurology 0
mohammad barzegar professor of pediatric neurology, pediatric health research center, tabriz university of medical sciences, tabriz, iran mohammad sayadnasiri assistant professor of neurology, department of neurology, qazvin university of medical sciences, qazvin, iran aidin tabrizi pediarician, pediatric health research center, tabriz university of medical sciences,tabriz, iran

how to cite this article: barzegar m, sayadnasiri m, tabrizi a. epilepsy as a rare neurologic manifestation of oculodentodigitalis dysplasia. iran j child neurol 2012; 6(3): 39-43. oculodentodigitalis dysplasia (oddd) is an extremely rare inherited disorderinvolving the development of the face, eyes, teeth and limbs. in addition,some patients develop neurological problems mostly a spastic parap...

Journal: :Journal of Korean Medical Science 1993
Y. Park G. Gong G. Choe E. Yu K. S. Kim I. Lee

Jarcho-Levin syndrome (JLS) is a condition manifested by malformations of vertebral bodes and related ribs. There are two major subtypes spondylocostal dysostosis and spondylothoracic dysostosis, with different survival rates, associated malformations, and inheritance patterns. We have experienced an autopsy case of a premature female fetus with multiple congenital anomalies. She was 30 weeks o...

Journal: :international journal of pediatrics 0
maria francis yuvaraj instructor, phd candidate, department of anatomy, saveetha medical college, thandalam, chennai, india. ponuswamy kasirajan sankaran associate professor, department of anatomy, saveetha medical college, thandalam, chennai, india. gunapriya raghunath professor, department of anatomy, saveetha medical college, thandalam, chennai, india. zareena begum kumaresan instructor, phd candidate, department of anatomy, saveetha medical college, thandalam, chennai, india. kumaresan kumaresan m instructor, phd candidate, department of anatomy, saveetha medical college, thandalam, chennai, india.

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...

Journal: :مجله دانشکده دندانپزشکی مشهد 0
نوشین نوشین محتشم nooshin mohtasham associate professor, dept of oral and maxillofacial pathology, school of dentistry and dental research center of mashhad university of medical sciences, mashhad, iranدانشیار گروه آسیب شناسی دهان، فک و صورت دانشکده دندانپزشکی و مرکز تحقیقات دندانپزشکی دانشگاه علوم پزشکی مشهد نصرالله نصرالله ساغروانیان nasrollah saghravanian assistant professor, dept of oral and maxillofacial pathology, school of dentistry and dental research center of mashhad university of medical sciences, mashhad, iranاستادیار گروه آسیب شناسی دهان، فک و صورت دانشکده دندانپزشکی و مرکز تحقیقات دندانپزشکی دانشگاه علوم پزشکی مشهدسازمان اصلی تایید شده: دانشگاه علوم پزشکی مشهد (mashhad university of medical sciences) نوریه نوریه شریفی noorieh sharifi associate professor, dept of pathology, ghaem hospital, mashhad university of medical sciences, mashhad, iranدانشیار گروه آسیب شناسی بیمارستان قائم دانشگاه علوم پزشکی مشهدسازمان اصلی تایید شده: دانشگاه علوم پزشکی مشهد (mashhad university of medical sciences) محمد تقی محمد تقی شاکری mohammadtaghi shakeri associate professor, dept of epidemiology, ghaem hospital, mashhad university of medical sciences, mashhad, iranدانشیار گروه اپیدمیولوژی و آمار حیاتی بیمارستان قائم دانشگاه علوم پزشکی مشهدسازمان اصلی تایید شده: دانشگاه علوم پزشکی مشهد (mashhad university of medical sciences) شیما شیما عامل قریب shima amelgarieb dentistدندانپزشکسازمان اصلی تایید شده: دانشگاه علوم پزشکی مشهد (mashhad university of medical sciences) ستاره ستاره شجاعی setareh shojaee postgraduate student, dept of oral and maxillofacial pathology, dental school, mashhad university of medical sciences, mashhad, iranدستیار تخصصی گروه آسیب شناسی دهان و فک و صورت دانشکده دندانپزشکی دانشگاه علوم پزشکی مشهد

introduction: leukoplakia is the most common precancerous lesion of the oral mucosa and may range microscopically form benign hyperkeratosis to invasive squamous cell carcinoma. p53 is a tumor suppressor protein; whereas, proliferative cell nuclear antigen (pcna) is a proliferative marker. the aim of this study was to evaluate the immunohistochemical expressions of p53 and pcna in oral leukopla...

Journal: :iranian journal of medical sciences 0
mitra basiratnia shiraz nephrology-urology research center, shiraz university of medical sciences, shiraz, iran alireza baradaran-heravi child and family research institute, department of medical genetics, university of british columbia, vancouver, canada majid yavarian hematology research center, shiraz university of medical sciences, shiraz, iran bita geramizadeh department of pathology, shiraz university of medical sciences, shiraz, iran mehran karimi hematology research center, shiraz university of medical sciences, shiraz, iran

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 first tim...

Journal: :acta medica iranica 0
m. eslami f. baghaee m. alaeddini

it is sometimes difficult to recognize a jaw lesion as osteosarcoma, ossifying fibroma or ‎fibrous dysplasia in routine hematoxylin and ‎eosin staining and a more accurate technique is needed to differentiate these ‎lesions. ‎many studies have shown the potential usefulness of silver-stained nucleolar organizer region (agnor) parameters for the diagnosis of various neoplasms. this study was car...

علایی , عبدالرسول, غفاری ساروی , وجیهه,

Çamptomelic dysplasia is a fatal infantile dysplasia characterized by lower limb bowing and mesomelic dwarfism. Most of this skeletal dysplasia occur through spontaneous mutation, but recessive autosomic recession is also likely. Prenatal diagnosis is considered with ultrasonography and amniocentesis. Postnatal diagnosis is characterized by mesomelic dwarfism with limb bowing, pulmonary h...

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