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By studying the families pedigree chart
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Are you allowed to drink alcohol if you have Cystic fibrosis?
Yes, but I wouldn't recommend it. The alcohol might possibly destroy some meds in your body and make you dizzy and sick. Check with your doctor to check whether or not the alcohol will affect your body.
What did Francis Collins discover?
He discovered genes causing cystic fibrosis, neurofibromatosis, and Huntington Chorea. (i would spell check this answer) please look to further references.
What states do they drug test your newborn in?
They check your newborn in ALL STATES! THEY CHECK TO SEE IF THE NEWBORN IS HEALTHY.
Can an Adult get cystic fibrosis?
From what I understand there is no such thing as Adult Onset Cystic Fibrosis. CF is a hereditary genetic disease that you are born with. That said, there are rare cases of people with symptoms so mild they were not diagnosed until there 30s-60s. Sometimes these people have had prior medical problems but their doctors didn't check for CF because of their age. It is often so debilitating that children are diagnosed within the first few days of life. I am not an expert, I am just looking for research because I was told to go in for a test today (at age 33). The hospital couldn't even administer the test in the normal lab, I need to go to the children's hospital. I am just now reading http://www.cff.org/ it has more official information.
Your wife is your mothers sisters daughter can you have a healthy baby?
Probably. BUT, there is also the possibility of compounding any genetic disease that the family has--such as Huntington's disease, cystic fibrosis and the like. Check with your state laws to see if marrying a first cousin is legal.
What do you do if your newborn hasn't pooped since birth?
It depends on how long it is. If it more than a couple of days then go to the doctor to check for constipation.
Cystic fibrosis?
DefinitionCystic fibrosis is an inherited disease that causes thick, sticky mucus to build up in the lungs and digestive tract. It is one of the most common chronic lung diseases in children and young adults, and may result in early death.See also:Cystic fibrosis - nutritional considerationsNeonatal cystic fibrosis screeningCauses, incidence, and risk factorsCystic fibrosis (CF) is caused by a defective gene which causes the body to produce abnormally thick and sticky fluid, called mucus. This mucus builds up in the breathing passages of the lungs and in the pancreas, the organ that helps to break down and absorb food.This collection of sticky mucus results in life-threatening lung infections and serious digestion problems. The disease may also affect the sweat glands and a man's reproductive system.Millions of Americans carry the defective CF gene, but do not have any symptoms. That's because a person with CF must inherit two defective CF genes -- one from each parent. An estimated 1 in 29 Caucasian Americans have the CF gene. The disease is the most common, deadly, inherited disorder affecting Caucasians in the United States. It's more common among those of Northern or Central European descent.Most children with CF are diagnosed by age 2. A small number, however, are not diagnosed until age 18 or older. These patients usually have a milder form of the disease.SymptomsBecause there are more than 1,000 mutations of the CF gene, symptoms differ from person to person.Symptoms in newborns may include:Delayed growthFailure to gain weight normally during childhoodNo bowel movements in first 24 to 48 hours of lifeSalty-tasting skinSymptoms related to bowel function may include:Belly pain from severe constipationIncreased gas, bloating, or a belly that appears swollen (distended)Nausea and loss of appetiteStools that are pale or clay colored, foul smelling, have mucus, or that floatWeight lossSymptoms related to the lungs and sinuses may include:Coughing or increased mucus in the sinuses or lungsFatigueNasal congestion caused by nasal polypsRecurrent episodes of pneumonia. Symptoms in someone with cystic fibrosis include: FeverIncreased coughingIncreased shortness of breathLoss of appetiteMore sputumSinus pain or pressure caused by infection or polypsSigns and testsA blood test is available to help detect CF. The test looks for variations in a gene known to cause the disease. Other tests use to diagnose CF include:Immunoreactive trypsinogen (IRT) test is a standard newborn screening test for CF. A high level of IRT suggests possible CF and requires further testing.Sweat chloride test is the standard diagnostic test for CF. A high salt level in the patient's sweat is a sign of the disease.Other tests that identify problems that can be related to cystic fibrosis include:Chest x-ray or CT scanFecal fat testLung function testsMeasurement of pancreatic functionSecretin stimulation testTrypsin and chymotrypsin in stoolUpper GI and small bowel seriesTreatmentAn early diagnosis of CF and a comprehensive treatment plan can improve both survival and quality of life. Follow-up and monitoring are very important. If possible, patients should be cared for at cycstic fibrosis specialty clinics, which can be found in many communities. When children reach adulthood, they should transfer to a cystic fibrosis specialty center for adults.Treatment for lung problems includes:Antibiotics to prevent and treat lung and sinus infections. They may be taken by mouth, or given in the veins or by breathing treatments. People with cystic fibrosis may take antibiotics only when needed, or all the time. Doses are usually higher than normal.Inhaled medicines to help open the airwaysDNAse enzyme replacement therapy to thin mucus and make it easier to cough upFlu vaccine and pneumococcal polysaccharide vaccine (PPV) yearly (ask your health care provider)Lung transplantis an option in some casesOxygen therapy may be needed as lung disease gets worseTreatment for bowel and nutritional problems (see: Cystic fibrosis - nutritional considerations) may include:A special diet high in protein and calories for older children and adults (see: Cystic fibrosis nutrional considerations)Pancreatic enzymes to help absorb fats and proteinVitamin supplements, especially vitamins A, D, E, and KYour doctor can suggest other treatments if you have very hard stoolsCare and monitoring at home should include:Avoiding smoke, dust, dirt, fumes, household chemicals, fireplace smoke, and mold or mildewClearing or bringing up mucus or secretions from the airways. This must be done one to fours times each day. Patients, families, and caregivers must learn about doing chest percussion and postural drainage to help keep the airways clearDrinking plenty of fluids. This is particularly true for infants, children, in hot weather, when there is diarrhea or loose stools, or during extra physical activityExercising two or three times each week. Swimming, jogging, and cycling are good options. Avoid contact sports, scuba diving, and endurance activities such as marathonsSupport GroupsFor additional information and resources, see: Cystic fibrosis support groupExpectations (prognosis)Most children with cystic fibrosis are fairly healthy until they reach adulthood. They are able to participate in most activities and should be able to attend school. Many young adults with cystic fibrosis finish college or find employment.Lung disease eventually worsens to the point where the person is disabled. Today, the average life span for people with CF who live to adulthood is approximately 35 years, a dramatic increase over the last three decades.Death is usually caused by lung complications.ComplicationsThe most common complication is chronic respiratory infection.Bowel problems, such as gallstones, intestinal obstruction, and rectal prolapseCoughing up bloodChronic respiratory failureDiabetesInfertilityLiver diseaseor liver failure, pancreatitis, biliary cirrhosisMalnutritionNasal polyps and sinusitisOsteoporosisand arthritisPneumonia, recurrentPneumothoraxRight-sided heart failure (cor pulmonale)Calling your health care providerCall your health care provider if an infant or child has symptoms of cystic fibrosis.Call your health care provider if a person with cystic fibrosis develops new symptoms or if symptoms get worse, particularly severe breathing difficulty or coughing up blood.Call your health care provider if you or your child experiences:Fever, increased coughing, changes in sputum or blood in sputum, loss of appetite, or other signs of pneumoniaIncreased weight lossMore frequent bowel movements or stools that are foul-smelling or have more mucusSwollen belly or increased bloatingPreventionThere is no way to prevent cystic fibrosis. Screening those with a family history of the disease may detect the cystic fibrosis gene in 60 - 90% of carriers, depending on the test used.ReferencesBoat TF, Acton JD. Cystic fibrosis. In: Kliegman RM, Behrman RE, Jenson HB, Stanton BF, eds. Nelson Textbook of Pediatrics.18th ed. Philadelphia, Pa: Saunders Elsevier; 2007:chap 400.Farrell PM, Rosenstein BJ, White TB, et al. Guidelines for diagnosis of cystic fibrosis in newborns through older adults: Cystic fibrosis consensus report. Journal of Pediatrics. Aug 2008;153(2).Stallings VA, Stark LF, Robinson KA, Feranchak AP, Quinton H. Evidence-based practice recommendations for nutrition-related management of children and adults with cystic fibrosis and pancreatic insufficiency: Results of a systematic review. Journal of the American Dietetic Association. May 2008;108(5).Yankaskas JR, Marshall BC, Sufian B, et al. Cystic fibrosis adult care: consensus conference report. Chest. 2004;125(1 suppl):1S-39S. Review.Mogayzel PJ Jr, Flume PA. Update in cystic fibrosis 2009. Am J Respir Crit Care Med. 2010 Mar 15;181(6):539-44.Tuchman LK, Schwartz LA, Sawicki GS, Britto MT. Cystic fibrosis and transition to adult medical care. Pediatrics. 2010 Mar;125(3):566-73.Borowitz D, Robinson KA, Rosenfeld M, et al. Cystic Fibrosis Foundation evidence-based guidelines for management of infants with cystic fibrosis. J Pediatr. 2009 Dec;155(6 Suppl):S73-93.
Can a newborn penguin walk?
I think so check penguin books
Is a wobbly neck in a newborn a symptom of Foetal Alcohol Syndrome?
Not necessarily--some babies are that way just because they have not reached that development level. It varies. In any case, support the baby's head until it can do so. Check in with your doctor.
Should check for newborn be made out to parents or newborn?
Make it out to the parents. The newborn will not have a social security number so you will be giving them extra hoops to jump through in order to cash it. You might also consider savings bonds for the child.
When will the doctor check for a heartbeat?
When the doctor comes in the room they will check your heartbeat, ears, and eyes.
What does CI means in blood work levels?
In various blood work panels, doctors check for levels of chloride (CI). Chloride is an electrolyte that comes from salt and can be measured in urine or in the blood. Its purpose is to maintain a good balance of fluids in your body. It is often checked when signs of dehydration are present. There is also a sweat test that measures chloride levels to help doctors determine if a child is suffering from cystic fibrosis.
