Hearing loss in Iranian children with cystic fibrosis
نویسندگان
چکیده
منابع مشابه
Prevalence of Cystic Fibrosis Trans-membrane Conductance Regulator Gene common mutations in children with cystic fibrosis in Isfahan, Iran
Background: Cystic fibrosis (CF) is the most common lethal genetic disorder of Cystic Fibrosis Trans-membrane Conductance (CFTR) Regulator gene mutations. We aimed to investigate common mutations in CF patients and to assess its possible relationship with clinical presentations. Materials and Methods: This cross sectional study was conducted on 36 CF patients who were referred to a tertiary ped...
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Background and purpose: Proper resonance is a major factor for the comprehension of speech in individuals with hearing loss. These people have low speech intelligibility caused by inappropriate resonance. Therefore, nasalance measurement is a principal aspect of the assessment of people with hearing loss. This study aimed at determining nasalance in children with hearing loss. Materials and me...
متن کاملClinical Presentations of Cystic Fibrosis in Iranian Children
Cystic Fibrosis (CF), characterized by abnormal transport of chloride and sodium ion across the epithelium, leads to thick, viscous secretions (1). The hallmark signs and symptoms of cystic fibrosis are salty tasting skin, poor growth and poor weight gain despite a normal food intake, accumulation of thick, sticky mucus, frequent chest infections, and coughing or shortness of breath. Males can ...
متن کاملCYSTIC FIBROSIS Airway remodelling in children with cystic fibrosis
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...
متن کاملIdentification of Dermatoglyphic Patterns in Parents of Children with Cystic Fibrosis
Background Dermatoglyphics could assist in the diagnosis of congenital abnormalities. The aim of this study was to identify the dermatoglyphic patterns (finger print pattern type, total ridge count of each finger, a-b ridge count, and articulotrochanteric distance [ATD angles]) in the parents of cystic fibrosis children. Materials and Methods We recruited 75 parents of children with cystic fibr...
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ژورنال
عنوان ژورنال: Medical Journal of Tabriz University of Medical Sciences and Health Services
سال: 2019
ISSN: 1608-5671,2008-160X
DOI: 10.34172/mj.2019.004