पुटीमय क्षोभाचा किंवा व्रणाच्या ठिकाणच्या पेशीजालात होणारी पेशीजालांची निर्मिती काय आहे

प्रती आहेत 30,000 अमेरिकन व्यक्ती आणि 70,000 पुटीमय क्षोभाचा किंवा व्रणाच्या ठिकाणच्या पेशीजालात होणारी पेशीजालांची निर्मिती ग्रस्त की जगभरातील (CF), फिजिशियन बद्दल निदान 1,000 प्रत्येक वर्षी नवीन प्रकरणे.

CF परिणाम घाम करा की शरीरात पेशी, पाचक द्रव आणि पदार्थ. साधारणपणे, या शरीर सहजतेने काम ठेवा की फार निसरडा आणि नंतर प्रणाली आहेत. मात्र, आपण CF असेल तर, ते झाले जाड आणि सरस. शरीराच्या आत काळा नळ्या आणि ducts या निधी उद्भवणार.
CF लोक अवघड वेळ श्वास करता तीव्र आणि सक्तीचे फुफ्फुसाचा संसर्ग होतो.

जादा वेळ, पदार्थ आपल्या श्वसनमार्गांवर आत गोळा; हे एक संघर्ष श्वास करते. श्लेष्मल सापळे जंतू संसर्ग ठरतो. IT can also cause severe lung damage like a cyst (fluid-filled sacs) and fibrosis (scar tissue). That is how CF got its name.

Symptoms of CF

People with CF have several symptoms, Including;

  • Very Salty -tasting skin
  • Non-stop coughing, at times generating phlegm
  • Frequent lung infections including bronchitis and pneumonia
  • Poor growth or weight gain in spite of a healthy appetite
  • Wheezing or shortness of breath
  • Frequent greasy, or bulky stools, difficulty with bowel movement
  • Male infertility

What Causes Cystic Fibrosis?
It is not contagious; It is produced by a deviation (change) within a single gene described as the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR,) This controls the flow of salt and fluids in and out of your cells. If the CFTR gene does not work as it should, glutinous mucus mounts up throughout your body.
To get CF, you have to receive a mutated copy of the gene from both your parents.
If you only inherit one copy, you will not exhibit any symptoms, But you will be a carrier for the disease. That indicates there’s a possibility you could pass it on to your child one day.
बद्दल 10 million Americans are CF carriers. Every time two CF carriers have a baby, there is a 25% (1 आणि 4) chance that their baby will be born with Cystic Fibrosis. There is a 50% chance the child will be a carrier but not have CF. There is a 25% chance that the child will not carrier CF gene or have CF.

Which Portions of the body does CF affect?
The lung is not the only part of the body that is affected by CF. CF also impacts the Liver, स्वादुपिंड, small intestines, large intestine,
and kidneys, Bladder and Reproductive organs.
People with Cystic Fibrosis have the greater risk of developing lung infection because of sticky mucus build up, creates an environment in which germs can thrive and grow. Lung infections are caused mostly by bacteria and tend to be a very serious problem.

  • यकृत: If the tubes that transport bile become plugged, your liver get inflamed, and severe scarring or cirrhosis occurs.
  • स्वादुपिंड: The thick mucus caused by CF block ducts in your pancreas. This stops digestive enzymes (proteins that break down your food) from reaching your intestine; as a result, your body has a difficult time absorbing the nutrients it needs. Over time this can also lead to diabetes.
    Small intestine- Since breaking down high-acid foods that come from the stomach is difficult, the lining of the small intestine can start to erode.
  • Large intestine: Thincscreations (liquids) in the stomach can make feces very thick. This can trigger blockages, IN some cases the intestine may also start to fold in on itself like an accordion in disorder called intussusception.
  • Bladder: Chronic coughing weakens the bladder muscles, Almost 65 of omen with CF suffer from stress incontinenceThis means that you leak urine when you sneeze, खोकला, laugh or try to lift something, Although this is more common in women, it can occur in men.
  • मूत्रपिंड: Some people with CF get kidneys stones. These small, hard mineral deposits can generate nausea, उलट्या होणे, and pain. If ignored, they can lead to a kidney infection.
  • Reproductive organs: surplus mucus affects fertility in both men and women. Most men with CF have problems with the tubes that transport their sperm, or what;s called the vasa differentia. Women with CF have very thick cervical mucus, which can make it harder for sperm to fertilize an egg.
  • Other parts of the body: Cystic Fibrosis can also lead to thinning of the bones or osteoporosis ) आणि स्नायू कमकुवत. Since CF upsets the balance of minerals in the blood, it can also produce lower blood pressure, थकवा, a fast heart rate and overall feeling of weakness.

Treatments for Cystic Fibrosis:
The type of severity of CF symptoms can differ based on the person. So it’s important to have a treatment plan that contains elements that are unique to each’s situation.
People with CG should work closely with their medical providers and families to create personalized treatment plans.
Look to the CF Foundation, which accredits more than 120 विशेष रोग व्यवस्थापन रुग्णांना काळजी मदत करण्यासाठी CF समर्पित तज्ञ कार्यरत आहेत संगोपन केंद्रे.

प्रत्येक दिवस, CF लोकांना साधारणपणे खालील चिकित्सा संयोजन आहे:

  • सोडविणे मदत आणि फुफ्फुसं तयार होऊ शकत नाही की जाड पदार्थ परिहारणे विमानाचा मंजुरी, काही विमानाचा मंजुरी तंत्र कुटुंब काही मदत आवश्यक असू शकते, मित्र किंवा श्वसन थेरपिस्ट. CF सह अनेक लोक आणि सोडविणे मदत करण्यासाठी एक inflatable छाती वर एक उच्च नाडी येथे थकलेला आणि vibrates आहे की बंडी पातळ पदार्थ वापर.
  • इनहेल विमानाचा मार्ग किंवा पातळ पदार्थ उघडण्यासाठी. हे एक nebulizing माध्यमातून धुके किंवा द्रवपदार्थाचा बारिक फवारा मध्ये केले जातात आणि घेतला की द्रव औषधे आहेत. Tese औषधे स्पष्ट श्वसनमार्ग मदत करण्यासाठी फुफ्फुसात संक्रमण लढण्यासाठी प्रतिजैविक आणि चिकित्सा समावेश.
  • स्वादुपिंडाच्या सजीवांच्या शरीरात निर्मार्ण होणारे द्रव्य परिशिष्ट कुपी महत्वाच्या पोषक शोषण सुधारण्यास मदत करण्यासाठी. या पूरक प्रत्येक जेवण आणि सर्वात snacks सह घेतले आहेत. CF लोक सहसा multivitamins होतील.

CF दररोज काळजी आवश्यक आहे एक गंभीर स्थिती आहे, तरी, तो अनेक उपचार प्रगत आहे. CF आहे असे लोक ते वापरू पेक्षा जास्त काळ राहतात आणि जीवन गुणवत्ता खूप सुधारणा झाली आहे.