Review of Short Phrases and Links|
This Review contains major "Cystic Fibrosis"- related terms, short phrases and links grouped together in the form of Encyclopedia article.
- Cystic fibrosis is a genetic disorder involving the pancreas and the lungs.
- Cystic fibrosis is a failure in the chloride channels.
- Cystic fibrosis is the most common cause of chronic pancreatitis in children.
- Cystic fibrosis is one of the most common life-shortening, childhood-onset inherited diseases.
- Cystic fibrosis is a particularly cruel disease, causing the lingering deaths of teenagers and young adults.
- Includes nutritional links to disorders such as Down syndrome, cerebral palsy, homocystinuria, and cystic fibrosis.
- Cerebral palsy research; Cystic fibrosis research; Hemophilia research; and Sickle cell disease research.
- CYSTIC-FIBROSIS: im. IMMUNITY. PSEUDOMONAS-AERUGINOSA: im.
- Cystic fibrosis is diagnosed by testing sweat and by testing lung or pancreas function.
- Rickets in adult cystic fibrosis with myopathy, pancreatic insufficiency and proximal renal tubular dysfunction.
- Shwachman H, Lebenthal E, Khaw W. Recurrent acute pancreatitis in patients with cystic fibrosis with normal pancreatic enzymes.
- Smyth RL, van Velzen D, Smyth AR, Lloyd DA, Heaf DP. Strictures of ascending colon in cystic fibrosis and high-strength pancreatic enzymes.
- Ironically, the healthy gene is named "CFTR" (cystic fibrosis transmembrane regulator).
- Merelle ME, et al. (2002). Newborn screening for cystic fibrosis.
- Taussig, L., et al. 1983. Neonatal screening for cystic fibrosis. Pediatrics 72(6):741-744.
- We suggest that mixed (Jewish and non-Jewish) Caucasian couples should be offered cystic fibrosis carrier screening.
- Witt H. Chronic pancreatitis and cystic fibrosis.
- Mutations of the cystic fibrosis gene in patients with chronic pancreatitis.
- Cohn JA, Bornstein JD, Jowell PS. Cystic fibrosis mutations and genetic predisposition to idiopathic chronic pancreatitis.
- Causative for respiratory disease and pancreatic dysfunction are mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene.
- Preimplantation genetic diagnosis (PGD) of cystic fibrosis by multiplex PCR combining deltaF508 mutation and intragenic microsatellites of the CFTR gene.
- Identification of the cystic fibrosis gene: genetic analysis.
- Newborn screening for cystic fibrosis is important because more than 10 million Americans are symptomless carriers of a cystic fibrosis gene.
- Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA. Science.
- Cystic fibrosis and Tay-Sachs disease are transmitted as recessive disorders.
- DNA tests are used for disorders such as cystic fibrosis, Tay-Sachs, or sickle-cell anemia.
- Gives information on cystic fibrosis, sickle cell anemia, hemophilia, PKU, ADA SCID, and muscular dystrophy.
- It is estimated that 10% of the cases of cystic fibrosis (CF) and 15% of the cases of Duchenne muscular dystrophy (DMD) are due to nonsense mutations.
- After cystic fibrosis (CF), it is the second most common cause of exocrine pancreatic insufficiency in children.
- Durie PR. Pancreatitis and mutations of the cystic fibrosis gene.
- Review. PMID 1743211 ^ Kulczycki LL, Shwachman H. Studies in cystic fibrosis of the pancreas; occurrence of rectal prolapse.
- Borowitz DS, Grand RJ, Durie PR. Use of pancreatic enzyme supplements for patients with cystic fibrosis in the context of fibrosing colonopathy.
- SO Am-J-Dis-Child. 1974 May. 127(5). P 746-7. MJ CYSTIC-FIBROSIS: co.
- More information regarding CF is available through the Cystic Fibrosis Foundation (http://www.cff.org).
- Grey VL, Lands L. Glutathione status in patients with Cystic Fibrosis. Canadian Cystic Fibrosis Foundation. $66,446. 2001.
- Cystic Fibrosis Foundation - Greater Michigan Chapter, Eastern RegionProvides education, service and research.
- Genetic determination of exocrine pancreatic function in cystic fibrosis.
- Fecal elastase-1 cut-off levels in the assessment of exocrine pancreatic function in cystic fibrosis.
- Early decline of pancreatic function in cystic fibrosis patients with class 1 or 2 CFTR mutations.
- Cystic fibrosis with normal sweat chloride concentration: case report.
- This causes chloride to flow out, and water follows. In cystic fibrosis, cAMP fails to activate the chloride channels.
- When steatorrhea is present without chronic respiratory abnormalities, a sweat test may be performed to help exclude a possible diagnosis of cystic fibrosis.
- Effect of pancreatic enzymes on zinc absorption in cystic fibrosis.
- Pancreatic enzyme replacement therapy in cystic fibrosis: Australian guidelines.
- Maintenance of growth in cystic fibrosis despite reduction in pancreatic enzyme supplementation.
- Cystic Fibrosis news, links and chat room.
- BioSpace News: Cystic fibrosis - News on new developments with Cystic Fibrosis.
- Subclinical vitamin K deficiency in cystic fibrosis.
- Excessive faecal losses of vitamin A (retinol) in cystic fibrosis.
- Andersen DH. Cystic fibrosis of the pancreas, vitamin A deficiency and bronchiectasis.
- Allan JD, Mason A, Moss AD. Nutritional supplementation in treatment of cystic fibrosis of the pancreas.
- Cystic fibrosis (CF) is a genetic disease.
- Cystic fibrosis (CF) is the most common, life threatening genetic disorder in Australia.
- Carriers of specific cystic fibrosis mutations are also at increased risk to have CBAVD.
- ISSN: 02776715. Cheng K, Ashby D, Smyth R. Oral steroids for cystic fibrosis. The Cochrane Database of Systematic Reviews.
- Cystic fibrosis occurs when there is a mutation in the CFTR gene.
- Correlation of sweat chloride concentration with classes of the cystic fibrosis transmembrane conductance regulator gene mutations.
- Aim: To examine the relationship between cystic fibrosis transmembrane regulator gene mutations (CFTR) and in vivo transepithelial potentials.
- There is also DNA testing, which tells if there are two cystic fibrosis gene mutations present in the body.
- Genetic Testing for Cystic Fibrosis.
- Symposium Mucoviscidosis (cystic fibrosis), Nijmegen.
- International Conference of the Baltic and North Countries on Cystic Fibrosis.
- Cystic fibrosis is found most commonly in people of northern European or UK descent.
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- Abnormal electrolyte composition of sweat in cystic fibrosis of the pancreas: clinical implications and relationship to the disease.
- Andersen first described cystic fibrosis of the pancreas.
- PMID 9725922 ^ Malfroot A, Dab I. New insights on gastro-oesophageal reflux in cystic fibrosis by longitudinal follow up.
- Riordan JR. The cystic fibrosis transmembrane conductance regulator.
- Ledson, MJ, Tran, J, Walshaw, MJ. Prevalence and mechanisms of gastro-oesophageal reflux in adult cystic fibrosis patients.
- Parents of a child with cystic fibrosis are taught by hospital staff how to do this.
- Carpentieri U, Gustavson LP, Haggard ME. Misdiagnosis of neglect in a child with bleeding disorder and cystic fibrosis.
- Comparison of fecal elastase-1 determination with the secretin-cholecystokinin test in patients with cystic fibrosis.
- Improved respiratory prognosis in patients with cystic fibrosis with normal fat absorption.
- Serum lipase after secretin stimulation detects mild pancreatic involvement in cystic fibrosis.
- Serum lipase levels pre and post Lundh meal: evaluation of exocrine pancreatic status in cystic fibrosis.
- Related Articles Update on the evaluation of pancreatic exocrine status in cystic fibrosis.
- An increased risk of pancreatic cancer has also been found in cystic fibrosis [59, 60].
- Weber AM, Roy CC, Chartrand L. Relationship between bile acid malabsorption and pancreatic insufficiency in cystic fibrosis.
- Preconception and prenatal carrier screening for cystic fibrosis.
- A baby born with only one cystic fibrosis gene and not a pair is only a carrier of the disease.
- If you inherit only one cystic fibrosis gene, you are called a carrier and do not have symptoms.
- Cystic fibrosis population carrier screening: 2004 revision of American College of Medical Genetics mutation panel.
- Use of fecal elastase-1 to classify pancreatic status in patients with cystic fibrosis.
- Elastase-1 is superior to fecal chymotrypsin in the assessment of pancreatic involvement in cystic fibrosis.
- Relation between mutations of the cystic fibrosis gene and idiopathic pancreatitis.
- The cystic fibrosis transmembrane conductance regulator gene and ion channel function in patients with idiopathic pancreatitis.
- Mutations of the cystic fibrosis gene, but not cationic trypsinogen gene, are associated with recurrent or chronic idiopathic pancreatitis.
- In addition, researchers are studying the genetics of hereditary pancreatitis, as well as risk factors such as cystic fibrosis.
- Evaluation of fecal pancreatic elastase-1 as a measure of pancreatic exocrine function in children with cystic fibrosis.
- Gentamicin-induced correction of CFTR function in patients with cystic fibrosis and CFTR stop mutations.
- A study of the relationship between neurological function and serum vitamin E concentrations in patients with cystic fibrosis.
- Improvement of fecal fat excretion after addition of omeprazole to pancrease in cystic fibrosis is related to residual exocrine function of the pancreas.
- Carl von Rokitansky described a case of fetal death with meconium peritonitis, complication of meconium ileus associated with cystic fibrosis.
- Prior to prenatal and newborn screening, cystic fibrosis was often diagnosed when a newborn infant failed to pass faeces ( meconium).
- Fecal elastase: pancreatic status verification and influence on nutritional status in children with cystic fibrosis.
- Nutritional benefits of neonatal screening for cystic fibrosis.
- Essential element nutritional status in cystic fibrosis.
- Rayner RJ, Littlewood JM. Vitamin A status as a marker of prognosis in cystic fibrosis.
- The effect of cimetidine on maldigestion in cystic fibrosis.
- Walkowiak J. Assessment of maldigestion in cystic fibrosis.
- METHODS: FE, indicating pancreatic lipase activity, was assessed in children (6.0 to 8.9 years of age) with cystic fibrosis and pancreatic insufficiency.
- Bollbach R, Becker M, Rotthauwe HW. Serum immunoreactive trypsin and pancreatic lipase in cystic fibrosis.
- Therapeutic potential and clinical efficacy of acid-resistant fungal lipase in the treatment of pancreatic steatorrhea due to cystic fibrosis.
- Children with cystic fibrosis, a progressive, disabling, and incurable lung disease, may also have pancreatitis.
- Relative contribution of genetic and nongenetic modifiers to intestinal obstruction in cystic fibrosis.
- BMJ. 2007 Dec 15;335(7632):1255---59. ^ Pai VB, Nahata MC. Efficacy and safety of aerosolized tobramycin in cystic fibrosis.
- Other autosomal disorders such as cystic fibrosis and sickle cell anemia are far more common.
- Cystic fibrosis represents the first genetic disorder elucidated strictly by the process of reverse genetics.
- Mutations in the cystic fibrosis gene in patients with congenital bilateral absence of the vas deferens.
- CBAVD, Congenital bilateral absence of the vas deferens; CF, cystic fibrosis; PI, exogenous pancreatic insufficiency; PS, exogenous pancreatic sufficiency.
- Hum Genet 1994;93:467470.[Medline] Oates RD, Amos JA. The genetic basis of congenital bilateral absence of the vas deferens and cystic fibrosis.
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