نتایج جستجو برای: phaces syndrome

تعداد نتایج: 621916  

Journal: :international journal of reproductive biomedicine 0
ashraf moini fatemeh javanmard bita eslami najmeh aletaha

background: polycystic ovarian syndrome (pcos) is a condition associated with chronic anovulation, insulin resistance and androgen excess. women with this syndrome are at increased risk of metabolic syndrome. objective: the aim of the present study was to determine the prevalence of metabolic syndrome (mbs) in women with pcos referred to arash hospital in different ages and body mass index (bmi...

Journal: :medical journal of islamic republic of iran 0
mohammad ebrahim parsanezhad p.o. box: 71345- 1657, shiraz-lran. mahnaz pakniat department of obstetrics and gynecology, school of medicine, shiraz university of medical sciences, shiraz, iran saeed alborzi department of obstetrics and gynecology, school of medicine, shiraz university of medical sciences, shiraz, iran ernst heinrich schmidt department of obstetrics and gynecology, evang diakrmie teaching hospital of the gottingen university, bremen, germany.

abstract background: in order to evaluate the role ofketoconazole in the prevention of ovarian hyperstimulation syndrome (ohss) in women with polycystic ovary syndrome (pcos) undergoing ovarian stimulation with gonadotropins, a prospective, randomized, double-blind, placebo controlled study was done on one-hundred and nine pcos women that had been refeited to be treated by gonadotropins. method...

ژورنال: یافته 2011
طایی, نادره, طرهانی, فریبا, عباسی, فرزانه,

Allgrove (AAA) syndrome or familial glucocorticoid deficiency or Tripple A Syndrome is a rare genetic disorder with transmitted autosomal recessive. Allgrove and colleagues first described this syndrome in 1978. Allgrove Syndrome characterized by Adrenal insufficiency, Alacrima and Achalasia. Neurological and dermatological findings may be presented in some patients. Hyperpigmentation and A...

Atyeh Ebadi Behrooz Barikbin Zahra Saffarian

Crouzon syndrome is a rare inherited autosomal dominant syndrome characterized by craniosynostosis, midface hypoplasia. Acanthosis nigricans may be associated with Crouzon syndrome, but it differs from the classic crouzon syndrome. This is a report of a 30-year-old-woman who presented acanthosis nigricans coexist with crouzon syndrome.

حبیب زاده, حسین, قانعی قشلاق, رضا, همتی مسلک پاک, معصومه,

Introduction: Restless legs syndrome is a neurological disorder hemodialysis patients seem to suffer more from this syndrome. Although the pathophysiology of restless legs syndrome is still unknown, assessment of factors associated with this syndrome can help to develop medical knowledge in this field. The present study assessed the relationship between restless legs syndrome, serum iron, and s...

حسینی, مصطفی , دانشی مسکونی, میلاد , صدرزاده یگانه, هاله , عزیزی, سمانه ,

Background: Food insecurity refers to the inability to afford enough food for an active, healthy life. The metabolic syndrome, otherwise known as syndrome X or the insulin resistance syndrome, is a collection of cardiovascular risk factors including hypertriglyceridemia, lowered HDL-cholesterol, glucose intolerance, abdominal obesity and hypertension. Recent studies indicate widespre...

Introduction: Hamartomatous Polyposis Syndromes (HPS) are a rare group of dominant autosomal inheritance, which is characterized by the development of hamartomatous polyps in the gastrointestinal tract.  This syndrome included Juvenile Polyposis syndrome (JPS), Peutz-Jeghers syndrome (PJS), and PTEN Hamartoma Tumour Syndrome (PHTS). PTEN Hamartoma Tumour Syndrome (PHTS) itself includes Cowden ...

Journal: :مجله دیابت و متابولیسم ایران 0
h fakhrzadeh p ebrahim pour m nouri r pourebrahim r heshmat p shoushtarizadeh

introduction: metabolic syndrome includes obesity, hypertriglyceridemia, glucose intolerance, hypertension and lipid profile abnormalities. the risk of cardiovascular diseases with this syndrome is higher than every components alone. in view of its burden and high mortality rate, this syndrome should be noted. methods: the 25-64 aged individuals in 17th zone of tehran were studied. it was desig...

احسانی‌پور, فهیمه,

    Introduction: Cornelia de lange syndrome(CDLS) is a rare syndrome which is characterized by multiple congenital anomalies, mental retardation, characteristic facial appearance, developmental delay, skeletal malformation, hirsutism, and various ophthalmologic problems. The diagnosis of this syndrome is clinical. Case Report: The patient of the present case report was an infant with cornelia ...

اسلامی, ابوالقاسم, رودپیما, شهلا,

Noonan syndrome is a genetic condition inherited by an autosomally dominant manner, characterised by congenital heart disease, short stature, abnormal facies and the somatic feature of Turner's syndrome, but a normal karyotype. Noonan syndrome affects approximately 1 in 1500 live births. Congenital heart disease occurs in 35-50% of patients diagnosed with noonan syndrome. The most common cardia...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید