نتایج جستجو برای: Hair disease

تعداد نتایج: 1521465  

Journal: :medical journal of islamic republic of iran 0
kobra shiasi arani research center for biochemistry and nutrition in metabolic disorders, kashan university of medical sciences, kashan, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی کاشان (kashan university of medical sciences)سازمان های دیگر: research center for biochemistry and nutrition in metabolic disorders

cartilage hair hypoplasia (chh), is a rare cause of metaphyseal chondrodysplasia and short stature. other features included hair abnormality, immunodeficiency, anemia, gastrointestinal disorders (hirschsprung disease, celiac, …) and increased risk of cancer. the disease is an autosomal recessive disorder and previously has not been reported in iran. we report a 9-year-old boy diagnosed as carti...

  Cartilage hair hypoplasia (CHH), is a rare cause of metaphyseal chondrodysplasia and short stature. Other features included hair abnormality, immunodeficiency, anemia, gastrointestinal disorders (Hirschsprung disease, celiac, …) and increased risk of cancer. The disease is an autosomal recessive disorder and previously has not been reported in Iran. We report a 9-year-old boy diagnosed as car...

Journal: :iranian journal of otorhinolaryngology 0
amir hossain ghazizadeh department of otorhinolaryngology, shahid beheshti university of medical sciences, tehran, iran. mehdi bakhshaee ear, nose, throat, head and neck surgery research center, mashhad university of medical sciences, mashhad, iran ebrahim mahdavi audiologist, shahid beheshti university of medical sciences, tehran, iran. rahman movahhed department of otorhinolaryngology, faculty of medicine, mashhad university of medical sciences, mashhad, iran

introduction: it has been shown that low levels of pigmentation increase susceptibility to noise-induced hearing loss in humans. for this reason, white populations develop more pronounced noise- induced hearing loss in comparison to black populations. similarly, blue-eyed individuals exhibit greater temporary threshold shift than brown-eyed subjects; still, no strong correlation has been verifi...

Journal: :iranian biomedical journal 0
سمیرا گیلانچی samira gilanchi بنفشه اسماعیل زاده banafshe esmaeilzade اکرم عیدی akram eidi محمود براتی mahmood barati ثریا محرابی soraya mehrabi فاطمه مغنی قرقی fatima moghani ghoroghi ملیحه نوبخت

background: the seladin-1 (selective alzheimer disease indicator-1), also known as dhcr24, is a gene found to be down-regulated in brain region affected by alzheimer disease (ad). whereas, hair follicle stem cells (hfsc), which are affected in with neurogenic potential, it might to hypothesize that this multipotent cell compartment is the predominant source of seladin-1. our aim was to evaluate...

Journal: :iranian journal of allergy, asthma and immunology 0
sayyed hesamedin nabavizadeh mojgan safari reza amin

kawasaki disease is a multi system disorder with varying clinical expressions. this disease is an acute systemic vasculitis of unknown etiology that has recently recognized as a leading cause of acquired heart disease in children of many developed countries. we describe an unusual instance of hair loss in a patient with kawasaki disease. a 26 months old boy developed prolonged high fever, bilat...

Journal: :iranian biomedical journal 0
بنفشه اسمعیل زاده banafshe esmaeilzade ملیحه نوبخت maliheh nobakht محمدتقی جغتایی mohammad taghi joghataei ناهید رهبر روشندل nahid rahbar roshandel هما رسولی homa rasouli علی صمدی کوچک سرایی ali samadi kuchaksaraei سید محمد حسینی

background: alzheimer’s disease (ad) is characterized by progressive neuronal loss in hippocamp. epidermal neural crest stem cells (epi-ncsc) can differentiate into neurons, astrocytes and oligodendrocytes. the purpose of this study was to evaluate the effects of transplanting epi-ncsc into ad rat model. methods: two weeks after induction of ad by injection of amyloid-β 1-40 into ca1 area of ra...

سیدمحمد موذنی, , علیرضا صالحی نوده, , پروین منصوری, ,

Background: Alopecia areata is a common, inflamatory and chronic disease of hair and nails, which in some cases result in growth inhibition and lose of hairs. Several factors such as genetic factors, autoimmunity, atopy, stress, fear etc, are known as effective factors in induction and severity of the disease, but the ethiology of this disease is not known exactly so far. Some evidences such as...

ژورنال: پوست و زیبایی 2021
Banimohammad, Majid , Forghani Ramandi, Mahdi , Pazoki Toroudi, Hamidreza ,

Alopecia areata (AA) is a sudden non-scarring hair loss that can be seen in any hairy area in the form of round or oval patches. It is an autoimmune disorder with an immunological response against hair follicles that is caused by genetic and environmental factors. The prevalence of AA is about 0.1% to 0.2% worldwide. Depending on the severity of the disease and sites of involvement, it can be d...

ژورنال: پوست و زیبایی 2015
خضریان, لیلا, فیضیان, مهتاب, موسوی, لیلا, یزدانفر, آمنه,

Background and Aim: Cicatricial alopecia refers to lesions that result in permanent and irreversible hair loss and are associated with destruction of hair follicles. In this alopecias the hair follicle is replaced with connective tissue. After remission of initial infection or inflammation, hair regrowth is unlikely. Methods: In this retrospective cross-sectional study, 222 patients with cic...

Background Hair is an ectodermal structure, and its formation is regulated by master genes important in embryology. Hair shaft consists of three major regions: the medulla, cortex and cuticle. Hair shaft abnormality will divide structural hair abnormalities into two broad categories - those associated with increased hair fragility and those not associated with increased hair fragility. We condu...

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