نتایج جستجو برای: children cystic fibrosis

تعداد نتایج: 588220  

Journal: :Archives of disease in childhood 1995
S Ghosal C J Taylor M Pickering J McGaw N Beckles-Willson J K Wales

Monthly increments of length, weight gain, and head circumference were recorded from birth to 4 years of age in 52 children with cystic fibrosis. At birth the children showed stunting. Standard deviation (SD) scores at birth for height, weight, and head circumference were -1.24, -0.72, and -1.82 respectively. Over the first four years, length and weight SD scores showed a consistent improvement...

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Journal: :Archives of disease in childhood 2001
M P Villa J Pagani V Lucidi S Palamides R Ronchetti

AIM To investigate whether children with cystic fibrosis under 3 years of age have disordered breathing and episodes of oxygen desaturation during sleep. METHODS We studied 19 infants (9 boys and 10 girls) with cystic fibrosis, mean age 13.1 months (range 3-36 months) and 20 age and sex matched healthy subjects. Patients and controls underwent an overnight polysomnographic study and respirato...

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Journal: International Journal of Pediatrics 2019
Ali Akbar Velayati, Ali Valinejadi, Maryam Hassanzad, Masoumeh Ansari, Seyed Javad Sayedi,

Background Cystic fibrosis (CF) is the most prevalent lethal chronic genetic and multivariate disease, widespread in Iranian population. The aim of this study was to evaluate the condition of patients with CF from various dimensions in the last decades in Iran.<b...

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Journal: International Journal of Pediatrics 2020
Ali Akbar Sayyari, Amirhossein Hosseini, Beheshteh Olang, Farid Imanzadeh, Katayoun Khatami, Mahmoud Hajipour, Naghi Dara, Parastoo Ashtigoo, Pejman Rohani, Saleheh Tajalli, Sayeh Hatefi, Seyed Ramin Madani, Zahra Fazeli Farsani,

Background: Malnutrition is one of the most common disorders among children with Cystic Fibrosis (CF). The present study aimed to investigate the effect of nutritional consultation on the type and severity of malnutrition in children with CF. Materials and Methods: This quasi-experimental stud...

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2017

With the advent of new treatments for medical diseases such as cancer, asthma, HIV infection, and cystic fibrosis, more children and adolescents are living with chronic illness than ever before. Seventy years ago, persons with cystic fibrosis survived an average of 5 years, while currently the life expectancy for patients with cystic fibrosis is more than 30 years.1 For children with cancer, th...

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Journal: :مجله بین المللی زیست و زیست پزشکی 0
mohammad reza esmaeili dooki non-communicable pediatric diseases research center, babol university of medical sciences, babol, iran haleh akhavan-niaki genetic laboratory of amirkola children’s hospital, babol university of medical sciences, babol, iran soraya shabani genetic laboratory of amirkola children’s hospital, babol university of medical sciences, babol, iran reza tabaripour department of cellular and molecular biology, islamic azad university, babol-branch, iran

cystic fibrosis is an autosomal recessive disease caused by a wide spectrum of mutations in the gene encoding for the cystic fibrosis transmembrane conductance regulator protein. these mutations that correlate with different phenotypes, vary in their frequency and distribution in different populations. in this study missense mutation r117h that associated with the different clinical symptoms wa...

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Journal: :journal of comprehensive pediatrics 0
soheila khalilzadeh pediatric respiratory disease research center, nritld, masih daneshvari hospital, shahid beheshti university of medical sciences, ir iran +98-2127122458, p_nritld@yahoo.comسازمان های دیگر: pediatric respiratory disease research center, nritld mohamad reza boloursaz pediatric respiratory disease research center, nritld, masih daneshvari hospital, shahid beheshti university of medical sciences, ir iran +98-2127122458, p_nritld@yahoo.comسازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences)سازمان های دیگر: pediatric respiratory disease research center, nritld nooshin baghaie pediatric respiratory disease research center, nritld, masih daneshvari hospital, shahid beheshti university of medical sciences, ir iran +98-2127122458, p_nritld@yahoo.comسازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences)سازمان های دیگر: pediatric respiratory disease research center, nritld elaheh heydarian fard pediatric respiratory disease research center, nritld, masih daneshvari hospital, shahid beheshti university of medical sciences, ir iran +98-2127122458, p_nritld@yahoo.comسازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences)سازمان های دیگر: pediatric respiratory disease research center, nritld maryam hassanzad pediatric respiratory disease research center, nritld, masih daneshvari hospital, shahid beheshti university of medical sciences, ir iran +98-2127122458, p_nritld@yahoo.com; pediatric respiratory disease research center, nritld, masih daneshvari hospital, shahid beheshti university of medical sciences, ir iran +98-2127122458, p_nritld@yahoo.comسازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences)سازمان های دیگر: pediatric respiratory disease research center, nritld habib emami tobacco prevention and control research center, nritld, masih daneshvari hospital, shahid beheshti university of medical sciences, ir iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences)سازمان های دیگر: tobacco prevention and control research center, nritld

background cystic fibrosis (cf) is a genetic disease with an autosomal recessive pattern of inheritance. cf caused by a mutation in the cystic fibrosis transmembrane conductance regulator (cftr) gene and characterized by impaired transport of chloride ions across the cell membrane. staphylococcus aureus, pseudomonas aeruginosa, and burkholderia cepacia have been identified in the cultures of re...

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Journal: :Archives of disease in childhood 1996
P Lykavieris O Bernard M Hadchouel

Between 1960 and 1994 cystic fibrosis was found in nine out of 1474 infants investigated for neonatal cholestasis. Four had delay in passing meconium. In all patients cholestatic jaundice was present during the first 48 hours and in three patients cholestasis was complete, mimicking biliary atresia. Serum cholesterol concentrations were normal in all but two children. Sweat chloride was repeate...

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2007
Tom N Hilliard Nicolas Regamey Janis K Shute Andrew G Nicholson Eric W F W Alton Andrew Bush Jane C Davies

Background: The relationship between airway structural changes and inflammation is unclear in early cystic fibrosis (CF) lung disease. A study was undertaken to determine changes in airway remodelling in children with CF compared with appropriate disease and healthy controls. Methods: Bronchoalveolar lavage and endobronchial biopsy were performed in a cross-sectional study of 43 children with C...

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Journal: :The European respiratory journal 2011
A M Jones W Flight B Isalska M Cullen K Mutton A Bowling D Riley K Webb R Bright-Thomas

REFERENCES 1 Jones AM, Govan JR, Doherty CJ, et al. Spread of a multiresistant strain of Pseudomonas aeruginosa in an adult cystic fibrosis clinic. Lancet 2001; 358: 557–558. 2 Cheng K, Smyth RL, Govan JR, et al. Spread of b-lactam-resistant Pseudomonas aeruginosa in a cystic fibrosis clinic. Lancet 1996; 348: 639–642. 3 Armstrong DS, Nixon GM, Carzino R, et al. Detection of a widespread clone ...

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