Respiratory Cystic Fibrosis: Overview, Anatomy, Physiology, Treatment, and Patient Needs

Respiratory cystic fibrosis

Overview
Cystic fibrosis us the inherited disorder that is marked by the abnormality
in the human body's water, salt, and mucus-producing cells. The
respiratory CF is although not curable and gets worse with time
(University of Rochester medical centre2019). The quality treatment can
help people to live longer with the disorder most of this disorder live with
this disorder lives into their late 30s and majority into their 50s.

Anatomy of cystic fibrosis
CF causes thick mucus to develop and clog certain parts
of the human body such as lungs. This build-up is
produced by an atypical gene named the CFTR or cystic
fibrosis Trans-membrane controller. This CFTR regulates
the transportation of salt and H2O inside and outside of
the human body's cells.

Cont...
These are the little growth of tissue from the lining of the nose.
Nearly 30 000 kids and youngsters in the US and 70 000 persons
worldwide suffer from CF (Grief, 2008).
Some of the major body parts and systems specifically affected
by CF are;
Bronchioles
Small intestine
The male reproductive organs
cervical canal
The musculoskeletal system