نتایج جستجو برای: a case

تعداد نتایج: 13594969  

Apert syndrome is a genetic defect which was first described by Eugene Apert in 1906. itchr('39')s incidence is approximately one in 50000 births. This syndrome is many abnormalities in your body and Central Nervous System. rehabilitation can increase children and their parentchr('39')s quality of life.We report a case of Apert syndrome and his occupational therapy program.

Journal: :journal of minimally invasive surgical sciences 0
mansoure vahdat endometriosis and gynecologic disorders research center, iran university of medical sciences, tehran, iran samaneh rokhgireh endometriosis and gynecologic disorders research center, iran university of medical sciences, tehran, iran; endometriosis and gynecologic disorders research center, iran university of medical sciences, tehran, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی ایران (iran university of medical sciences) ashraf sadat mousavi endometriosis and gynecologic disorders research center, iran university of medical sciences, tehran, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی ایران (iran university of medical sciences) kobra tahermanmanesh endometriosis and gynecologic disorders research center, iran university of medical sciences, tehran, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی ایران (iran university of medical sciences) sepideh khodaverdi endometriosis and gynecologic disorders research center, iran university of medical sciences, tehran, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی ایران (iran university of medical sciences) leila nazari endometriosis and gynecologic disorders research center, iran university of medical sciences, tehran, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی ایران (iran university of medical sciences)

conclusions patient characteristics has important role in suture material degradation. impaired suture hydrolysis in uterus incision may cause abnormal uterine bleeding. it is interesting to demonstrate whethersuture degradation in previous cesarean section has a role in formation of placenta accrete or not .this issue needs more investigation. because there is no similar case in literature, we...

Journal: :iranian journal of pathology 2012
jahanbanoo shahryari shahriar dabiri amin talebi

kimura’s disease (kd) is a chronic inflammatory disorder primarily seen in male asians during the second and third decades of life. clinically, it presents as solitary or multiple subcutaneous nodules, predominantly in the head and neck region, typically in the pre auricular region, forehead, and scalp. the etiology of kimura disease is still unknown. this disorder should be suspected when the ...

Journal: :journal of dental materials and techniques 0
maryam baharvand department of oral medicine, dental school, shahid beheshti university of medical sciences, tehran, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences) shabnam sabounchi department of community oral health, hamadan university of medical sciences, hamadan, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی همدان (hamadan university of medical sciences) hamed mortazavi department of oral medicine, dental school, shahid beheshti university of medical sciences, tehran, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences)

salivary mucocele is a common lesion derived from minor salivary glands with various surgical or non-surgical treatment modalities. to evaluate the effect of a highly potent corticosteroid (dexamethasone) in the management of salivary mucocele, we performed intralesional injection of dexamethasone in nine patients with labial mucocele. complete healing of lesions observed in seven of nine patie...

K. Mardanpour Mahtab Rahbar,

Osteosarcoma of the foot is rare and, when presents, commonly observed in adults. We report a case of osteosarcoma of the calcaneus in an 11-year-old girl who was presented with a 4-month history of pain and swelling on her left ankle and inability to walk in her left lower extremity. On examination, there was a diffuse swelling involving her left ankle joint and foot. The radiograph showed sof...

Ali Hadipour, Elham Jafari, Hamid Pakmanesh, Najmeh sadat Fadaei

Adrenal myelolipoma is a rare benign tumor that is composed of hematopoietic cells and mature fat. Mostly, these nonfunctioning tumors are distinguished incidentally during autopsy or radiologic investigations. Here, we report a case of 46-year-old man presented with nonspecific abdominal pain for one year, who had right adrenal mass with fat density detected by radiologic investigation. Histop...

Background: Neonatal tumors are usually prenatally diagnosed or within the irst 30 days of life. The true incidence ofneonatal tumors is unknown as a great number of pregnancies with a prenatally diagnosed mass result in stillbirth ormiscarriage. Most solid neonatal tumors are benign whereas less than 50% of neonatal neoplasms are malignant;however, some tumors with malignant ...

A Rasi S Mirzazadeh Javaheri

Actinic prurigo is a rare disease occurring mainly in individuals of American Indian origin and those living in high altitudes. Skin lesions consist of pruritic popular or nodular excoriated lesions mainly affecting exposed skin but covered skin is also involved in up to 50% of patients. This is the first case report of an Iranian patient. This 19-year-old female had pruritic popular and ...

Abdelbaki Boukerche, Abdessamad Arabi, Lila Charef, Mohamed Bey, Mohamed-Amine Bekadja, Samira Bouchama,

Non Hodgkin Lymphomas (NHL) are nodal or extra nodal monoclonal infiltrations by malignant lymphoid cells (B Lymphocytes in 80% of cases), which are distinguished as indolent or aggressive forms. According to the heterogeneity of lymphoid cells and their ubiquitous anatomical distribution, these disorders can develop in any organ and have very heterogeneous clinical expressions, but they are...

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