Mucoviscidosis
Mostrando 1-6 de 6 artigos, teses e dissertações.
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1. Limiares auditivos em frequências ultra-altas em pacientes com fibrose cística : estudo caso-controle
Objetivo: Avaliar limiares auditivos através de audiometria em frequências ultra-altas (UHF) para detecção precoce de alterações auditivas assintomáticas nos pacientes com Fibrose Cística (FC). Material e métodos: Estudo transversal, tipo caso-controle, incluindo 69 indivíduos de 7 a 20 anos, 35 do grupo em estudo (GE) - com FC e 34 do grupo contro
Publicado em: 2009
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2. Vivendo com Fibrose Cística: a experiência da doença no contexto familiar / Living with Cystic Fibrosis: the disease experience in the familiar context.
Cystic Fibrosis, also known as Mucoviscidosis, is a chronic disease of autosomal recessive origin and so far incurable. The present study aimed to understand the experience of Cystic Fibrosis in the familiar context of children carriers. The subjects of the study are children with Cystic Fibrosis under follow-up at a university hospital from an interior city
Publicado em: 2008
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3. The structure of the breast in mucoviscidosis
The histological appearances of the breast in a patient with mucoviscidosis are those of complete lobular agenesis. Ducts and ductules are well developed, and there is abundant fibrous tissue giving the breast a normal contour. The appearances are contrasted with those of gynaecomastia, and the aetiology is discussed.
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4. Congenital mesonephric defects in male infants with mucoviscidosis
Reports that men with mucoviscidosis were sterile and that portions of their genital tracts were atretic prompted us to investigate the genital tracts of 15 male infants with mucoviscidosis who died within the first year of life and came to necropsy. The genital tracts of all of these infants were abnormal, the abnormalities being confined to mesonephric der
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5. Pulmonary changes and cor pulmonale in mucoviscidosis
The lungs of eight cases of cystic fibrosis in patients ranging from age 19 days to 23 years were examined by the large-section technique of Gough and Wentworth (Gough, 1960). All cases showed in life a susceptibility to staphylococcal and pseudomonal bronchopneumonia. In all cases the bronchial tree was plugged with mucus. The lungs from the older patients
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6. A comparison of changes in the mucous glands and goblet cells of nasal, sinus, and bronchial mucosa
A comparison of mucous gland size in the bronchial and nasal mucosa was performed on material from 24 random necropsies. The Reid index and counts of mucous gland acini were used as measures of hypertrophy. In 14 of these cases the relationship between goblet cell hyperplasia in the sinus mucosa and the presence of chronic bronchitis was investigated by comp