نتایج جستجو برای: golins syndrome
تعداد نتایج: 621911 فیلتر نتایج به سال:
night eating syndrome is a common disorder in eating behaviors that occurs in close relation to the night time sleep cycle. although eating disorders are common in society, night eating syndrome has been left neglected by health care professionals. in this report we present a case of eating disorder that exhibits some novel features of night eating syndrome. our case was a progressed type of ea...
conclusions the young woman with turner syndrome have several risk factors for early coronary artery disease development. in such cases, dramatic results like sudden death or heart attack at an early age may occur in cases of insufficient follow-up and treatment. case presentation the patient, a 27-year-old female was admitted to the emergency room with chest pain at rest. she was diagnosed wit...
purpose : to report an unusual presentation of chandler syndrome case report : a 22-year-old female came to our clinic with complaint of progressive visual loss in her left eye since three days ago. she had a history of trauma with finger-nail to her left eye eight days ago and had been managed with topical antibiotic. in her examination, the left eye had visual acuity (va) of counting finger a...
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...
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...
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...
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.
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...
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 ...
نمودار تعداد نتایج جستجو در هر سال
با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید