Vertaal "تشوه وراثي ويمكن" na Engels

EN This does not necessarily mean an inherited abnormality exists and may be associated only with a mild increase in the risk of cancer.

• does not necessarily
• inherited abnormality exists

EN This does not necessarily mean an inherited abnormality exists and may be associated only with a mild increase in the risk of cancer.

• does not necessarily
• inherited abnormality exists

EN These changes can be related to a genetic defect

• genetic defect

EN If you have a congenital heart defect, make an appointment with your doctor for follow-up care, even if you haven't developed complications

• congenital heart defect
• follow-up care
• developed complications

EN Here, a hole between the heart's main pumping chambers (ventricular septal defect) causes increased blood flow to the lungs' arteries

• main pumping chambers
• ventricular septal defect
• causes increased blood
• lungs' arteries

EN A ventricular septal defect (VSD), a hole in the heart, is a common heart defect that's present at birth (congenital)

• ventricular septal defect
• VSD
• common heart defect
• present at birth
• congenital

EN A small ventricular septal defect may cause no problems, and many small VSDs close on their own

• small ventricular septal
• cause no problems
• small VSDs close
• own

EN The tricuspid valve ? which is located between the right upper heart chamber (atrium) and the right lower chamber (ventricle) ? is malformed and often leaks.

• tricuspid valve
• upper heart chamber
• atrium
• right lower chamber
• ventricle
• malformed
• often

EN A bleeding brain AVM is life-threatening and requires emergency medical attention.

• bleeding brain AVM
• life-threatening
• requires emergency medical

EN Obvious deformity or shortening of the affected leg

• Obvious deformity
• leg

EN In Chiari malformation type 1, signs and symptoms usually appear during late childhood or adulthood.

• Chiari malformation type
• signs
• symptoms usually appear
• late childhood

EN Improper fluid drainage, perhaps because of a blockage or anatomic abnormality

• Improper fluid drainage
• blockage
• anatomic abnormality

EN Abnormalities of the testicles, penis or kidneys present at birth (congenital) might increase the risk of a scrotal mass and testicular cancer later in life.

• penis
• congenital
• scrotal mass
• testicular cancer later

EN Fibroids range in size from seedlings, undetectable by the human eye, to bulky masses that can distort and enlarge the uterus

• seedlings
• eye
• distort
• enlarge the uterus

EN Bone abnormalities may cause many people with Hunter syndrome to be abnormally short

• abnormally short

EN Malformed teeth, affecting dental enamel and roots, in cases when hypoparathyroidism occurs at an early age when teeth are developing.

• Malformed teeth
• affecting dental enamel
• roots
• cases when hypoparathyroidism

EN Basically, parts of the brain that control the functioning of your muscles and senses may be involved, even though no disease or abnormality exists.

• Basically
• control the functioning
• muscles
• abnormality

EN Signs and symptoms of body dysmorphic disorder include:

• Signs
• symptoms of body
• disorder

EN There's no known way to prevent body dysmorphic disorder

• There's no known
• prevent body dysmorphic

EN However, because body dysmorphic disorder often starts in the early teenage years, identifying the disorder early and starting treatment may be of some benefit.

• However
• because body dysmorphic
• early teenage years
• identifying the disorder

EN Long-term maintenance treatment also may help prevent a relapse of body dysmorphic disorder symptoms.

• Long-term maintenance treatment
• prevent a relapse
• body dysmorphic disorder

EN Signs and symptoms of body dysmorphic disorder include:

• Signs
• symptoms of body
• disorder

EN There's no known way to prevent body dysmorphic disorder

• There's no known
• prevent body dysmorphic

EN However, because body dysmorphic disorder often starts in the early teenage years, identifying the disorder early and starting treatment may be of some benefit.

• However
• because body dysmorphic
• early teenage years
• identifying the disorder

EN Long-term maintenance treatment also may help prevent a relapse of body dysmorphic disorder symptoms.

• Long-term maintenance treatment
• prevent a relapse
• body dysmorphic disorder

EN Cantaloupe may have discoloration or deformities on the rind; however, this does not mean it is bad. Check the inside before discarding.

• however
• does not mean
• bad
• Check the inside

EN Do not install a 140/280MM radiator in the inner side of the bracket otherwise irrepairable deformation might occur

• otherwise irrepairable deformation
• occur

EN Correct image distortion and noise

• Correct image distortion
• noise

EN In about 1% of people with COPD, the disease results from a genetic disorder that causes low levels of a protein called alpha-1-antitrypsin (AAt)

• COPD
• protein called
• AAt

EN Your doctor might suggest genetic counseling or screening if you plan to have children.

• doctor might suggest
• counseling

EN There also may be a genetic link to suicide

EN Various forms of muscular dystrophy, an inherited disease that causes progressive muscle weakness, can contribute to foot drop

• dystrophy
• progressive muscle weakness
• contribute to foot

EN Researchers believe the greater prevalence in these Asian countries strongly suggests a genetic factor in some populations.

• countries strongly suggests

EN If you have a family history of a genetic condition, getting genetic testing before you have symptoms may show if you're at risk of developing that condition

• genetic condition
• getting genetic testing
• symptoms may show
• you're at risk
• developing that condition

EN This form of the disease is not inherited and is often referred to as iron overload

• inherited
• iron overload

EN Genetics. OCD may have a genetic component, but specific genes have yet to be identified.

• Genetics
• genetic component

EN Sickle cell anemia ? a hereditary defect of hemoglobin in red blood cells ? causes blood in urine, both visible and microscopic hematuria

• Sickle cell anemia
• red blood cells
• both visible
• microscopic hematuria

EN Cystic fibrosis (CF) is an inherited disorder that causes severe damage to the lungs, digestive system and other organs in the body.

• Cystic fibrosis
• CF
• lungs
• digestive system

EN Because cystic fibrosis is an inherited disorder, it runs in families, so family history is a risk factor

• Because cystic fibrosis
• inherited disorder
• runs in families
• risk factor

EN Before you decide to be tested, you should talk to a genetic counselor about the psychological impact the test results might carry.

• Before you decide
• tested
• results might

EN Rarely, emphysema is caused by an inherited deficiency of a protein that protects the elastic structures in the lungs

• Rarely
• emphysema is caused
• protein that protects
• lungs

EN A genetic disorder that causes copper to accumulate in your liver (Wilson's disease)

• copper to accumulate
• liver
• Wilson's disease

EN A rare genetic disorder known as familial hypocalciuric hypercalcemia causes an increase of calcium in your blood because of faulty calcium receptors in your body

• rare genetic disorder
• familial hypocalciuric hypercalcemia
• increase of calcium
• body

EN Known carriers, who are using in vitro fertilization, may request a genetic test with fertilized eggs before implantation.

• Known carriers
• vitro fertilization
• request a genetic
• fertilized eggs before

EN Rett syndrome is a rare genetic neurological and developmental disorder that affects the way the brain develops, causing a progressive loss of motor skills and speech

• rare genetic neurological
• way the brain
• causing a progressive
• motor skills
• speech

EN Rett syndrome is a rare genetic disorder. Classic Rett syndrome, as well as several variants with milder or more-severe symptoms, can occur based on the specific genetic mutation.

• rare genetic disorder
• Classic Rett syndrome
• more-severe symptoms
• specific genetic

EN Children with the inherited form of retinoblastoma tend to develop the disease at an earlier age

• form of retinoblastoma
• develop the disease
• earlier age

EN Aortic aneurysms in younger people often have a genetic cause

• cause

EN Inherited disorders. Disorders such as Charcot-Marie-Tooth disease are hereditary types of neuropathy.

• Inherited disorders
• disease are hereditary

EN Cystine stones. These stones form in people with a hereditary disorder called cystinuria that causes the kidneys to excrete too much of a specific amino acid.

• Cystine stones
• hereditary disorder called
• causes the kidneys
• excrete too much
• specific amino