Pulmonary and Sleep Specialists in Michigan

Cystic Fibrosis Doctor in Michigan

Cystic Fibrosis Doctor in Oakland County and Wayne County Michigan

What is Cystic Fibrosis (CF)?

Cystic Fibrosis (CF) is a genetic disorder that primarily affects the respiratory and digestive systems. This condition, which is most commonly diagnosed in infancy or childhood, impacts approximately 70,000 individuals worldwide, with new cases being identified each year.

How is Cystic Fibrosis diagnosed?

Early detection and accurate diagnosis of Cystic Fibrosis are crucial to ensure optimal care and management of this condition. A combination of tests is typically employed for diagnosing CF, primarily including a sweat test that measures the amount of chloride in sweat (elevated levels indicate CF), as well as genetic testing to identify specific mutations associated with the disease.

Dr. Asker Asmi, MD is a certified pulmonologist, and sleep disorders doctor in Michigan

Social Links:
Dr. Asmi’s Beaumont Hospital Page
Dr. Asmi’s Henry Ford Profile Page

Dr. Asmi is a Pulmonologist and sleep specialist based in Michigan that specializes in advanced COPD. He follows a multidisciplinary treatment plan that includes nutrition, medicine, lifestyle changes, damage prevention and active treatment with close follow up. Doctor Asmi’s expertise include Critical Care Medicine, Pulmonary Medicine, Pulmonary Critical Care and Sleep Medicine. Dr. Asmi is also affiliated with Beaumont Hospital and runs a private practice in Riverview, MI.

What are the symptoms of Cystic Fibrosis?

CF manifests in various ways and can affect individuals differently; however, some common symptoms include persistent coughing, frequent lung infections, difficulty gaining weight or maintaining growth, salty-tasting skin, and difficulty digesting food. In later stages of CF, severe respiratory problems, including bronchiectasis and lung transplantation, may occur.

What are the causes of Cystic Fibrosis?

Cystic Fibrosis is caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. The CFTR protein regulates the movement of chloride ions within the body, particularly in the lungs and pancreas. Mutations in this gene lead to thickened mucus in these organs, making it difficult to breathe and digest food properly.

How is Cystic Fibrosis treated and managed?

Although there is currently no cure for CF, various treatments can help manage symptoms, improve quality of life, and slow disease progression. These include airway clearance techniques, medications like bronchodilators and anti-inflammatory drugs, nutritional support, and enzyme replacement therapy to aid in digestion.

Can Cystic Fibrosis be prevented?

There is no known prevention for Cystic Fibrosis since it is a genetic condition. However, early diagnosis and effective management of symptoms can help minimize complications and reduce the risk of transmission from one generation to the next. Individuals with a family history of CF are encouraged to discuss their risks with their healthcare provider.

FAQs (Frequently Asked Questions)

What is the life expectancy for individuals with Cystic Fibrosis?

Advancements in treatments and care have significantly increased the average lifespan for those living with CF, with many now reaching adulthood and beyond.

Can Cystic Fibrosis be passed down through generations?

Yes, CF is an inherited condition, meaning it can be passed from parents to their children. Carrier screening and genetic testing are essential for individuals with a family history of the disease.

Is there a cure for Cystic Fibrosis?

Currently, there is no cure for Cystic Fibrosis. However, ongoing research continues to explore potential treatments and therapies that may one day lead to a cure.