Lexic.us

Definition of Mucoviscidosis

1. Noun. The most common congenital disease; the child's lungs and intestines and pancreas become clogged with thick mucus; caused by defect in a single gene; no cure is known.

Medical Definition of Mucoviscidosis

1. An old name (but one that has prevailed in france and some other nations) for cystic fibrosis (cf), one of the most common and serious of all genetic (inherited) diseases. The cf gene is carried by 1/20 persons (in caucasian populations) and 1 in 400 couples is at risk for having children with cf. Cf is characterised by the production of abnormal secretions leading to mucous build-up. Which can impair the pancreas (and, secondarily, the intestine). Cf mucous build-up in lungs can impair respiration. Without treatment, cf results in death for 95% of children before age 5. Early diagnosis of cf is of great importance. Early and continuing treatment of cf is valuable. (12 Dec 1998)

Lexicographical Neighbors of Mucoviscidosis

Literary usage of Mucoviscidosis

Below you will find example usage of this term as found in modern and/or classical literature:

1. Disability in Higher Education by Serge Ebersold, Peter Evans (2003)
"... alcoholism Severe Migraine mucoviscidosis Bronchial asthma, medium degree Schizophrenic vulnerability with minor difficulties in social adaptation ..."

2. Digestive Diseases of the U. S.: Epidemiology and Impact edited by James E. Everhart (1994)
"sideroblastic (D64.0-D64.3) Includes: mucoviscidosis E84.1 Cystic fibrosis with intestinal manifestations ..."

3. Disability in Higher Education by Serge Ebersold, Peter Evans (2003)
"... alcoholism Severe Migraine mucoviscidosis Bronchial asthma, medium degree Schizophrenic vulnerability with minor difficulties in social adaptation ..."

4. Digestive Diseases of the U. S.: Epidemiology and Impact edited by James E. Everhart (1994)
"sideroblastic (D64.0-D64.3) Includes: mucoviscidosis E84.1 Cystic fibrosis with intestinal manifestations ..."

Other Resources: