Title, La enfermedad fibroquistica del pancreas: mucoviscosidosis. Author, Lea Rivelis. Publisher, Editorial Alfa, Length, pages. Export Citation. Estudio microbiológico de la flora de vias repiratorias de pacientes con Enfermedad Fibroquistica del Páncreas (FQ). I congreso Latinoamericano de Fibrosis. mal m; acute ~ enfermedad aguda; Alzheimer’s ~ enfermedad de Alzheimer; the bone enfermedad fibroquistica osea; fibrocystic ~ of pancreas enfermedad.

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Cystic FibrosisEnferedadFibrocystic disease of pancreas. These images are a random sampling from a Bing search on the term “Cystic Fibrosis. Search Bing for all related images.

Cystic fibrosis CF is an inherited disease of the mucus and sweat glands. It affects mostly your lungs, pancreas, liver, intestines, sinuses and sex organs.

enfermedar CF causes your mucus to be thick and sticky. The mucus clogs the lungs, causing breathing problems and making it easy for bacteria to grow. This can lead to problems such as repeated lung infections and lung damage. The symptoms and severity of CF vary widely. Some people have serious problems from birth. Others have a milder version of the disease that doesn’t show up until they are teens or young adults.

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Although there is no cure for CF, treatments have improved greatly in recent years. Until the s, most deaths from CF occurred in children and teenagers. Today, with improved treatments, some people who have CF are living into their forties, fifties, or older. Started inthis collection now contains interlinked topic pages divided into a tree of 31 specialty books and chapters.


Fibrosis Quística by Fernanda Mejía on Prezi

Content ddel updated monthly with systematic literature reviews and conferences. Although access to this website is not restricted, the information found here is intended for use by medical providers.

Patients should address specific medical concerns with their physicians. Hospitalization Indications References Extra: Related Bing Images Extra: Epidemiology Usually diagnosed in childhood Incidence in live births Caucasian: Pathophysiology Autosomal Recessive trait Exocrine gland disorder produces mucus blockage Blocks fine tubules in various organs.

Guido Fanconi (1892-1979)

Airway management Airway clearance Percussion and postural drainage Active cycle breathing Positive expiratory pressure mask Autogenic drainage Flutter valve Pneumatic vest Mucus fibroqiustica drugs Pulmozyme 2.

Nebulized Tobramycin Traditional Tobramycin Dose: Pneumonia Under age 10 years: Multiple organisms Age 10 and older: Hospitalization Indications Fibroqyistica cough Increased Sputum production or color change Anorexia and weight loss Exercise intolerance Malaise or irritability Decline in pulmonary function or CXR change.

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Porucha jejich funkce se projevuje zejm. This mucus can cause problems in digestion, breathing, and body cooling. Definition NCI A congenital metabolic disorder affecting the exocrine glands, inherited as an autosomal trait. The secretions of exocrine glands are abnormal, resulting in excessively viscid mucus production which causes obstruction of passageways including pancreatic and bile ducts, intestines, and bronchi.


fibrocystic disease of the pancreas – Spanish translation – Word Magic English-Spanish Dictionary

The sweat sodium and chloride content are increased. Symptoms usually appear in childhood and include meconium ileus, poor growth despite good appetite, malabsorption and foul bulky stools, chronic bronchitis with cough, recurrent pneumonia, bronchiectasis, emphysema, clubbing of the fingers, and salt depletion in hot weather.

Definition CSP most common potentially lethal autosomal recessive disease affecting Caucasians; characterized eenfermedad chronic pulmonary, intestinal, liver, pancreatic, and exocrine gland dysfunction; caused by mutations efermedad the CFTR chloride channel. Related Topics in Pediatrics. Pulmonology – Pediatrics Pages. Back Links pages that link to this page. Search other sites for ‘Cystic Fibrosis’.

National Heart, Lung, and Blood Institute. A common hereditary disease in which exocrine secretory glands produce abnormally thick mucus. A congenital metabolic disorder affecting the exocrine glands, inherited as an autosomal trait.

Disease or Syndrome T Cystisk fibroseMukoviskidoseMucoviscidosis.