Genetic mutations: Identifies mutations in the CFTR gene associated with cystic fibrosis. Respiratory function: Assesses the impact of the disease on the lungs and respiratory system. Pancreatic function: Reveals the effect of the disease on the production of digestive enzymes. Sweat chloride levels: High levels of salt in sweat may indicate the presence of the disease.

Children: Who show symptoms such as chronic cough, shortness of breath, or poor growth. Individuals with a family history of cystic fibrosis: To help determine potential genetic risk. Individuals with abnormal results in other tests: Such as sweat tests or respiratory assessments. Newborns: As part of newborn screening in some countries for early detection of the disease.

Chronic cough: Especially if accompanied by thick mucus. Shortness of breath: Or difficulty breathing. Recurrent lung infections: Such as pneumonia. Digestive problems: Such as poor nutrient absorption or fatty diarrhea. Poor growth: Or unexplained weight loss in children. Excessive sweating: Especially in hot weather.

What is the purpose of the test? It aims to diagnose cystic fibrosis by identifying genetic mutations. How is the test performed? It is usually done by taking a blood sample or performing a sweat test. Is any special preparation required before the test? The test generally does not require special preparation, but patients may be asked to avoid certain medications. What is the waiting period for results? Results usually take several days to a week. Is the cystic fibrosis test painful? Most people find the test painless or only slightly uncomfortable. What should I do if the result is positive? Discuss treatment options with your physician to determine the next steps. Can the test be performed on adults? Yes, it can be performed on adults, especially if they have symptoms or a family history.

Sweat test: Chloride levels in sweat below 30 mmol/L are considered normal. Levels between 30 and 60 mmol/L are considered a borderline range, while levels above 60 mmol/L often indicate a possible presence of cystic fibrosis. Genetic tests: Absence of known mutations in the CFTR gene is considered a normal result. Lung function tests: Values vary by age and gender, but generally, normal airflow measurement is a good indicator.

Cystic Fibrosis Genetic Test | Lahalak Platform

Advanced genetic testing to detect cystic fibrosis, enabling early diagnosis of respiratory and digestive disorders to ensure timely medical intervention and personalized care.

Prices starts from: 1253.25 SAR

Scientific name: Cystic Fibrosis Test

The cystic fibrosis test is considered a vital step in diagnosing cystic fibrosis. This hereditary disease primarily affects the mucus-secreting glands, leading to the accumulation of thick mucus in the lungs and other organs, which can cause serious respiratory and digestive problems. This test is based on analyzing genetic mutations associated wi...

Cystic Fibrosis Test - Comprehensive Cystic Fibrosis Test

Service type Laboratory test (Genetic)

Duration 10-15 minutes

Fasting Fasting is not required

Prices Starting from 1253.25 SAR

Included Services

Cystic Fibrosis Test
The optimal health guidance based on the result.
Personal support services from Lahalak

Medical Service Information

Purpose Test

Genetic mutations: Identifies mutations in the CFTR gene associated with cystic fibrosis.
Respiratory function: Assesses the impact of the disease on the lungs and respiratory system.
Pancreatic function: Reveals the effect of the disease on the production of digestive enzymes.
Sweat chloride levels: High levels of salt in sweat may indicate the presence of the disease.

Recommended groups

Children: Who show symptoms such as chronic cough, shortness of breath, or poor growth.
Individuals with a family history of cystic fibrosis: To help determine potential genetic risk.
Individuals with abnormal results in other tests: Such as sweat tests or respiratory assessments.
Newborns: As part of newborn screening in some countries for early detection of the disease.

Symptoms indicative

Chronic cough: Especially if accompanied by thick mucus.
Shortness of breath: Or difficulty breathing.
Recurrent lung infections: Such as pneumonia.
Digestive problems: Such as poor nutrient absorption or fatty diarrhea.
Poor growth: Or unexplained weight loss in children.
Excessive sweating: Especially in hot weather.

FAQs

What is the purpose of the test? It aims to diagnose cystic fibrosis by identifying genetic mutations.
How is the test performed? It is usually done by taking a blood sample or performing a sweat test.
Is any special preparation required before the test? The test generally does not require special preparation, but patients may be asked to avoid certain medications.
What is the waiting period for results? Results usually take several days to a week.
Is the cystic fibrosis test painful? Most people find the test painless or only slightly uncomfortable.
What should I do if the result is positive? Discuss treatment options with your physician to determine the next steps.

Normal Levels

Sweat test: Chloride levels in sweat below 30 mmol/L are considered normal. Levels between 30 and 60 mmol/L are considered a borderline range, while levels above 60 mmol/L often indicate a possible presence of cystic fibrosis.
Genetic tests: Absence of known mutations in the CFTR gene is considered a normal result.
Lung function tests: Values vary by age and gender, but generally, normal airflow measurement is a good indicator.