FIBROSE CISTICA PDF

A fibrose cística (FC), denominada também de mucoviscidose, é uma doença genética do tipo autossômica recessiva que acomete principalmente crianças e. O presente estudo examinou os desafios psicológicos de adolescentes com fibrose cística (FC) no Brasil, por meio de uma entrevista semiestruturada com. View at Google Scholar; L. F. O. Honório, N. Ludwig Neto, E. Barbosa et al., “ Avaliação da triagem neonatal para fibrose cística no estado de.

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Acute lymphoblastic leukemia Lymphoma. There is a great variety of endoscopic findings in CF patients and a trend toward increased incidence of diagnoses of nasal polyps over time. Resistance to the following have all been proposed as possible sources of heterozygote advantage:.

The focus of much CF gene therapy research is aimed at trying to place a normal copy of cisitca CFTR gene into affected cells. Sakano and coworkers [ 20 ], from Campinas Sao Paulo Statecollected samples using a swab of the oropharynx, secretions gathered by maxillary cistjca, and secretions gathered using endotracheal tubes, representing tracheal secretions from 50 CF patients. Quality of life and psychosocial development in adolescents with epilepsy: Computed tomography CT has become a valuable tool for the diagnosis and monitoring of disorders of the upper airway in CF patients and is cibrose essential in planning surgical cases, to study osseous structures.

Many of these symptoms occur when bacteria that normally inhabit the thick mucus grow out of control and cause pneumonia. It mixes features of type 1 and type 2 diabetes, and is recognized as a distinct entity, cystic fibrosis-related diabetes.

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Physical training in cystic fibrosis.

Wikimedia Commons has media related to Cystic fibrosis. These cystic formations, pseudomucoceles, led to protrusion of the lateral nasal wall and narrowing of the nasal cavity. The data compiled in this paper is useful, but also lead to the general agreement that more research would be welcome due to the unique characteristics of this country.

Parenting adolescents with cystic fibrosis: Most articles on this subject are European or American, involving both children and adults with CF. This prolonged therapy often necessitates hospitalization and insertion of a more permanent IV such as a peripherally inserted central catheter or Port-a-Cath.

Prática fisioterapêutica no tratamento da fibrose cística | Conto | ABCS Health Sciences

Assessment of percussion, vibratory-shaking and breathing exercises in chest physiotherapy. Nasal polyposis in CF patients was described for the first time in [ 21 ].

Transferring the normal CFTR gene into the affected epithelium cells would result in the production of functional CFTR protein in all target cells, without adverse reactions or an inflammation response.

Hoping to live a “normal” life whilst living with unpredictable figrose and fear of death: There were no differences in any parameter between D F homozygous and heterozygous patients.

The product of this gene the CFTR protein is a chloride ion channel important in creating sweat, digestive juices, and mucus. View at Google Scholar O. In airway epithelial cells, the cilia exist in between the cell’s apical surface and mucus in a layer known as airway surface liquid ASL. In addition to the pancreas problems, people with cystic fibrosis experience more heartburn[29] intestinal blockage by intussusceptionand constipation.

Psicologia em Estudo

Archived from the original on August 11, Therefore, most individuals are diagnosed after symptoms e. Several mechanical techniques are used to dislodge sputum and encourage its expectoration. The incidence of cystic fibrosis CF in Brazil varies among different regions 1: Subscribe to Table of Contents Alerts. These blockages lead to remodeling and infection in the lung, damage by accumulated digestive enzymes in the pancreas, blockage of the intestines by thick feces, etc.

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View at Google Scholar S. The gene for CF is located in chromosome 7, at locus q31, formed by kilobases of DNA, with 27 exons. In pediatric patients with CF and suspected mucocele, MRI is essential to help eliminate other entities such as meningocele, rhabdomyosarcoma, hemangioma, and neuroblastoma [ 48 ]. Testing is typically performed first on one or both parents and, if the risk of CF is high, testing on the fetus is performed.

The disease is caused by mutations in the gene encoding the cystic fibrosis transmembrane regulator protein CFTRmapped in the human chromosome at 7q Expert Review of Respiratory Medicine. Genetic disordermembrane: The mean age at onset of symptoms cistiva 3 months, and the mean age at diagnosis was 2 years and 4 months. One hundred and four patients were finrose Paediatric Nursing, 19 329— Fetal and maternal outcome”.

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The American College of Obstetricians and Gynecologists recommends all people thinking of becoming pregnant be tested to see if they are a carrier.