Cystic Sentence Examples

Thus Echinococci contains a leucomaine which sets up an urticaria; Cysticercus tenuicollis occasions anaemia and death if injecte-1 into rabbits; and the cystic fluid of the common Coenurus serialis is said to be used by Kirghizes to poison wolves.

The right and left hepatic ducts, while still in the transverse fissure, unite into a single duct which joins the cystic duct from the gall bladder at an acute angle.

The same description applies to the reptiles, but a curious net work of cystic ducts is found in snakes and to a less extent in crocodiles.

However, I have seen photos of people who had severe cystic acne who healed very well by taking Roaccutane.

Millions of parents have already used amniocentesis and sonograms to diagnose Down's syndrome or cystic fibrosis.

A woman discovered that she was a cystic fibrosis carrier during routine antenatal testing several years ago.

For this reason, we prefer to tie the cystic duct using a catgut Roeder external slip knot.

The disease gene is named CFTR, which stands for cystic fibrosis transmembrane conductance regulator.

During the Opening Ceremony of the 27th European cystic fibrosis Conference 2004, in Birmingham, Dr. Littlewood was awarded both the above honors.

The aim of the research is to understand, treat and cure cystic fibrosis.

Should deadly viruses be used to treat cystic fibrosis?

Genetic trail The test also allows detection of any of the genetic mutations which can cause cystic fibrosis.

The development and optimal management of acute and chronic lung disease, including cystic fibrosis, are also being studied.

It marks 40 years of achievement in fighting cystic fibrosis.

Autonomy Sarah is exercising her preference not to have a child affected by cystic fibrosis.

All of the medical research funded by the cystic fibrosis Trust is peer reviewed.

Patients with cystic fibrosis may be more prone to gastro-intestinal motility disturbances.

This is joined by the cystic duct from the gall bladder, which then forms the common bile duct.

The aim of the research is to understand, treat and cure Cystic fibrosis.

The entire event is run in aid of the cystic fibrosis Trust with each runner pledging to raise a minimum of £ 300.

After complete resection papillary cystic neoplasm has a good prognosis with a low rate of recurrence.

Underlying molecular defect CF is caused by mutations in the gene encoding the cystic fibrosis transmembrane conductance regulator (CFTR) protein.

Dermoid cyst (sometimes called benign mature cystic teratomas) These cysts can grow quite large - up to 15 cm across.

Recent studies have included people with treatment with schizophrenia, children with cystic fibrosis and adults with renal transplant.

Wristbands cystic Fibrosis wristbands cystic Fibrosis wristbands are on sale in the UK.

The gall-bladder, appropriately designated as "the bitter," was regarded as a part of the liver, and the cystic duct (compared, apparently, to a "penis") to which it is joined, as well as the hepatic duct (pictured as an "outlet") and the ductus choleductus (described as a "yoke"), all had their special designations.

X-ray on the right tibia revealed several osteolytic cystic lesions with sclerotic rims.

The sweat chloride test will not pick up carriers of cystic fibrosis.

These virulent pathogens cause inflammation in the lung in cystic fibrosis, killing many young adults with the disease.

Cystic hydatid disease is a Zoonosis caused by ingestion of E.G. eggs by contact with dog feces.

Mercury Redbone Celebrity Tournament Series - Gary Ellis and his wife Susan started this charity fishing event around 15 years ago to benefit the Cystic Fibrosis Foundation.

Some children with Marfan develop cystic disease of the lungs or recurrent spontaneous pneumothorax, which is a condition in which air accumulates in the space around the lungs.

Cystic fibrosis (CF) is an inherited disease that affects the lungs, digestive system, sweat glands, and male fertility.

Cystic fibrosis affects the body's ability to move salt and water in and out of cells.

Cystic fibrosis is a genetic disease, meaning it is caused by a defect in the person's genes.

The gene that, when defective, causes CF is called the CFTR gene, which stands for cystic fibrosis transmembrane conductance regulator.

A person with two mutated copies will develop cystic fibrosis.

The decision to test a child for cystic fibrosis may be triggered by concerns about recurring gastrointestinal or respiratory symptoms or salty sweat.

Adults with a family history of cystic fibrosis may obtain a genetic test of their carrier status for purposes of family planning.

Cystic fibrosis transmembrane conductance regulator (CFTR)-The protein responsible for regulating chloride movement across cells in some tissues.

Cystic fibrosis results when a person has two defective copies of the CFTR gene.

Some children seem to be more at risk for having GERD than others, particularly children who have hiatal hernia, cystic fibrosis, neurological impairment or delay, or an immature esophagus and LES.

Some chronic conditions, such as asthma, chronic bronchitis, emphysema, and cystic fibrosis, are characterized in part by a cough.

Congenital cystic adenomatoid malformation (CCAM) occurs when one or more lobes of the lungs develop into fluid-filled sacs called cysts rather than into normal lung tissue.

Congenital cystic adenomatoid malformation (CCAM)-A condition in which one or more lobes of the fetal lungs develop into fluid-filled sacs called cysts.

The sweat test is used to diagnosis cystic fibrosis (CF).

To ensure accuracy, sweat tests should be analyzed by a laboratory certified by the Cystic Fibrosis Foundation.

It can be an early clue that the infant may have cystic fibrosis.

Meconium ileus in newborns is caused by increased viscosity of waste products in the intestinal tract, and is sometimes secondary to cystic fibrosis.

By 1997, approximately 800 different diagnostic tests were available, most of them for hereditary genetic disorders such as Tay-Sachs disease, sickle cell anemia, hemophilia, muscular dystrophy, and cystic fibrosis.

In children, cystic fibrosis, aspiration problems, immunodeficiencies, and congenital or acquired lung malformation may increase the risk of pneumonia from S. pneumoniae.

Infants with cystic fibrosis are more likely to experience meconium ileus (obstruction of a dark green material in the intestine in newborns).

In children with cystic fibrosis in which meconium ileus becomes evident soon after birth, the prognosis is linked with the primary disease; the median age of survival for cystic fibrosis patients is 30 years.

These include cystic fibrosis, asthma, cerebral palsy, muscular dystrophy, and various immunodeficiency disorders.

Having cystic fibrosis also increases a child's risk for appendicitis.

Cystic Fibrosis (CF) is a genetic lung disease.

The fluid is then sent to a lab where it will be tested for genetic abnormalities like Down syndrome, cystic fibrosis, and spina bifida.

Down syndrome, cystic fibrosis, and spina bifida are some of the most common abnormalities that an amnio can detect.

Her wholesomeness is also seen in her non-acting pursuits, as she's very involved with the Cystic Fibrosis Foundation.

Other malabsorption diseases include Crohn's disease and cystic fibrosis.

Anecdotal customer reports suggest the supplement helped with irritable bowel syndrome symptoms, improved cystic acne, and helped reduce the incidence of candida overgrowth.

St. Jude Children's Research Hospital and the Cystic Fibrosis Foundation both focus on research and finding cures for childhood diseases such as cancer and cystic fibrosis.

According to reports, one in every 150 children born is autistic, making autism more prevalent than childhood cancers or cystic fibrosis, among other disorders.

Autism Treatment Network was inspired by the Cystic Fibrous Network.

Frankie Abernathy, an alum of the San Diego season, died of cystic fibrosis in 2007 after the show closely documented her illness.

This treatment may not work for those suffering from cystic acne.

For acne that is severe or persistent, and certain conditions such as cystic acne, medical treatments may fare better than over-the-counter products.

Isotretinoin is a very strong medicine taken orally to treat deeper cystic acne.

For very severe, stubborn, or cystic acne, a dermatologist may need to prescribe the appropriate medication and possibly use other techniques, such as laser treatments or microdermabrasion to treat the acne.

Patients with severe acne and cystic acne, especially, respond much better to the kind of care only a doctor can provide.

It is unique in that it effectively treats severe cystic acne, as well as acne that has resisted other treatments.

Blue light therapy is mainly used to treat cystic acne once other acne therapies have been exhausted.

Blue light therapy appears to improve cystic acne in some individuals, and seems to be most effective for inflammatory acne lesions.

A long cystic duct would point to a long reign of the king.

The gland spaces vary in size and many may show marked cystic formation.

Here it undergoes a change into a cystic or " metacestode " state.

The most remarkable feature of this cystic development is the formation in many genera of several internal buds within a common cyst, each of which forms an independent inverted scolex (Coenurus, Polycercus); or these internal vesicles may bud off a large number of scolices on their external surface (Staphylocystis).