Doctor insights on:
Is Cyanosis A Symptom Of Cystic Fibrosis
Nil to chromosomal: Cystic hygroma can be found in healthy babies or in babies born with chromosome abnormalities. The outcome is generally better for a baby that does not have a chromosome abnormality. About 60% of cystic hygromas result from chromosome abnormalities. Common disorders associated with cystic hygroma are turner syndrome and trisomies. ...Read more
Depends on genes: The risk of acquiring cystic fibrosis (CF) depends on whether the parents of a child are carriers for the gene. It is estimated that about 1 in 20 americans are carriers of the CF gene. In order for a child to acquire the disease, both parents must be carriers. If both parents are carriers, there is then a 25% chance that the child will acquire the disease. ...Read moreSee 1 more doctor answer
Yes, very: 96% of nodules found in a study of screening ct scans were not lung cancer. While we don't know for sure what they were, its almost certain that many were granulomas, a type of scar often caused by "histo". In some areas of the country almost half the population has lung nodules detectable on a ct and histo gets blamed for many of them, with or without proof. It usually requires no treatment. ...Read more
CF gene mutations: There are currently more than 1900 mutations that are known to cause cf. About 70% of CF pts in us have deltaf508 mutation, as 1 in every 25 persons is a carrier for this mutation. All these mutations result in abnormal activity of a protein called cftr which causes all the CF related problems. Genetic testing can give the specific mutation each pt has. Talk to your local CF center. ...Read more
See cff.org: For good info.Get a more detailed answer ›
Kind of...: Cystic fibrosis (CF) is a genetic disease. Patients with the disease are born with a defective gene that is part of the body's system for making mucus, sweat, and digestive fluids. Their mucus is therefore abnormally thick and causes blockages in the lungs, pancreas and other organs that damage them and make them prone to infections and other problems. ...Read more
PPH : In utero the lungs are not expanded and therefore the blood flow is impeded too. So the pressure in these vessels are high. When baby is born since the lung inflates the pressure in these vessel now slowly decrease dramatically. Pph is when the pressure in the vessels does not decrease and thereby difficult to deliver oxygen to the baby. It can resolve with medicines and sometimes without but usua. ...Read moreSee 1 more doctor answer
A Transition: Pphn (acronym) is a common finding. All fetuses have high pulmonary artery resistance because their lungs are collapsed (full of fluid as they're not breathing). When the baby is born and takes a deep breath, the expanded lungs lead to decrease resistance and pressure in lungs. In some babies, the pressure remains high, hence the term pphn. This will resolve if there are no other issues. ...Read moreSee 2 more doctor answers
Sometimes: Pleural effusions can occur for a variety of reasons. Cancer is a cause of pleural effusion. How serious it is generally depends upon the underlying cause and the amount of fluid. Temporary relief can be achieved with drainage of the effusion (called thoracentesis). ...Read moreSee 3 more doctor answers
Yes: Yes it is possible. Presentation of cystic fibrosis varies greatly, and it is possible, depending on your specific mutation (and other factors) to present at a later age. In order to prevent late diagnoses, all states now have a newborn screen in place for cystic fibrosis. ...Read moreSee 1 more doctor answer
I have family members with cystic fibrosis. Is it possible to start show the symptoms in my 20's?
Poor growth/GI: In some children, 1st sign of CF is poor growth with child being small for age. This may be subtle enough that child continues to follow a growth curve on the growth chart, but in the lower percentiles until growth flattens out. Others have loose greasy stools as 1st sign. Frequent "bronchitis"/"sinus infections" that are thought to be just that until someone asks if that's just too many. ...Read more
My 4 year old daughter has all the symptoms of cystic fibrosis, but has tested negative twice. Is there anything else it could be?
Cystic Fibrosis: It seems your daughter was referred to a peds pulmonologist by her pediatrician; different tests were done to rule out cf. Sometimes geneticist gets involved in testing if any diagnostic controversy. If she has lung issues, the pulmonary doctor will address that. If she has digestive issues, she should have been referred to gastro-enterologist. Talk to her pediatrician who is the best guide. ...Read moreSee 3 more doctor answers
I want to see if there's any additional therapy I can do for my boyfriend. He has cystic fibrosis and I'd like to try to help ease the symptoms.
CF center: First I wish him all the best and good health and thank you for caring for him, any cystic fibrosis patient should be followed by specialists in a cystic fibrosis center, if you haven't done that already, please check the cystic fibrosis foundation on the web for help, www.cff.org, goodluck ...Read more
Cough, poor growth: Common symptoms of cystic fibrosis include cough, wheeze, recurrent lung infections, poor growth, foul smelling stools, salty sweat, clubbing, and rectal prolapse. The more symptoms the greater the chance of having cystic fibrosis. Most infants today are diagnosed by newborn screening for CF before they develop any symptoms and early therapy can minimize disease symptoms. ...Read more
See cff.org: For good info.Get a more detailed answer ›
Visit Pediatrician: I would recommend discussing your concerns with your pediatrician and explain them to him/her. If your pediatrician agrees with your concerns then tests may be ordered to further look into the diagnosis of cystic fibrosis (cf). If the test suggests CF then you will be referred to a CF center. Your pediatrician may still refer you to a pediatric pulmonologist if concerns remain. ...Read moreSee 1 more doctor answer
Stinky poo: If your kid has poop that will clear a room from the stinky smell, and the sweat tastes like salt i might consider that diagnosis. Most will be well into those symptoms by 4. If your kid only has recurrent respiratory issues its more likely from other origins like allergies or asthma. Share your concerns with your doctor. ...Read more
Lipase wk 1: 30 (16-120), wk 2: 15 l (16-120). Is this indicative of cystic fibrosis? No other symptoms.
Are you symptomatic?: Isolated lab results (particularly essentially normal ones like the lipase levels you describe) are relatively meaningless unless taken in the context for which they were ordered. As a child, was cystic fibrosis suggested as a possible diagnosis? Why are, and what makes, you concerned regarding this disease? More specific testing is appropriate if suspicion of CF is warranted. ...Read more
Can men with atypical cystic fibrosis have children? I have 2 children, I have no symptoms of CF and I am 32 years old. Never tested for CF.
What are symptoms of cystic fibrosis and could a 19 year old be diagnosed with it or would they have been screened as a child in 1993?
CF : The symptoms of CF vary and there are many mutations associated with this genetic disorder. Some of the symptoms include, chronic cough, production of sputum, chronic pneumonia, digestive problems, especially with fat intake, sinusitis, diabetes. One negative screening test may not have adequately ruled out cf. If you suspect cf, a screening sweat test should be performed. ...Read moreSee 1 more doctor answer
Were all babies from 1997-present screened for Cystic fibrosis in the state of Texas? Also, at what age do the symptoms for cystic fibrosis set in?
No: If memory serves me well. CF was not added to the newborn screening program until later.About 10 years back, the state expanded its screening program from 5 to more than 25 conditions, including CF. The symptoms might present with bowel blockage at birth, obnoxious smelly stools in infancy or may not have obvious symptoms for years. There is some individual variation from case to case. ...Read more
I have a cystic fibrosis mutation that showed no symptoms for 15 years, or since birth. Is it possible for symptoms to develop now or in the future?
Confusing post: An estimated 1/26 Caucasians in the US carry at least one CF mutation. Other ethnic groups have a separate carrier status. Your post does not cite your real status, as a carrier of one or two of the dozen or so genetic mistakes that can be involved in CF. Without clarifying your status, it is impossible to give a clear answer. You are welcome to start over. ...Read more
Yes: The primary symptoms are pulmonary and digestive. Chronic lung disease and recurrent lung infections start early in life. Intestinal malapsortion because of digestive enzyme deficiency also occurs early. Other symptoms include meconium illius in the perinatal period, growth failure in childhood and a variety of symptoms in the second and third decades of life including diabetes. ...Read moreSee 1 more doctor answer
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