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Clinical Reviews

Cystic fibrosis, a diagnosis at Primary Care

Authors:

Martínez García MSa, Casado Sánchez MLb

aPediatra. CS San Blas. Parla, Madrid. España.
bPediatra. CS San Blas. Parla, Madrid. España.

Correspondence: MS Martínez. Email: mmartinez.gapm10@salud.madrid.org

Reference of this article.:

Martínez García MS, Casado Sánchez ML. Fibrosis quística, diagnóstico desde Atención Primaria. Rev Pediatr Aten Primaria. 2011;13:83-8.

Published in Internet: 06/04/2011

Abstract:

Cystic fibrosis (CF) is an autosomal recessive disease caused by mutations in the gene encoding the CF transmembrane conductance regulator. It is characterized by numerous clinical variations: airway obstruction and infection, maldigestion, delay of the development... The lung injury determines morbidity and mortality. CF has a great deal of genetic mutations, which produce different phenotypes. However, the diagnosis is not easy and criteria are constantly revised after the latest scientific research. Since we can suspect the illness before than some years ago and due to the neonatal screening and the early treatments, prognosis and survival have improved in comparison with the last century.

It is worth insisting on the fact that diagnosis at Primary Care is possible: knowing the illness, suspecting it and carrying out the neonatal screening.

We present two cases at a Primary Care Unit, one of them manifesting respiratory symptoms and the other one digestive ones.

Keywords: Cystic fibrosis. Primary Care. Diagnosis.


 


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ISSN 2174-4106  Publicación Open Acess, incluida en DOAJ, sin cargo por publicación.

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