Significados de hereditary disease em inglês

I have xeroderma pigmentosum-XPfor short- arareand frequently fatal genetic disorder.

This is a genetic disorder that most people have never heard of.

Beta-thalassemia is a genetic disorder caused by mutations in the beta-globin gene.

Are these advantages as important as removing a genetic disorder from my genome?

Let's pretend I carry the gene responsible for a genetic disorder.

Elevated expression of c-Myc is a frequent genetic abnormality seen in this malignancy.

Activating mutations in ras genes are a common genetic abnormality in human malignancies.

It's a genetic abnormality.' I watch her reach into the fridge, rummaging around.

Understanding specific genetic abnormality may potentially lead to better treatment strategies in these patients.

Sebaceous carcinoma is sometimes found concurrently with visceral cancers and a genetic abnormality, Muir-Torre syndrome.

It must have been a genetic defect, because she was only twenty-two.

Peutz-Jeghers syndrome is an uncommon genetic defect in the signal pathways of growth.

The genetic defect in a number of rare disorders of metal metabolism remains elusive.

We report a novel genetic defect in a patient with type I Glanzmann thrombasthenia.

This genetic defect inevitably impacts in vivo sensitivity to PERV infection of these species.

So, could this be some kind of congenital disease that causes dementia-likeearly Alzheimer's?

Heterozygous mutation of the CHD7 gene causes a severe congenital disease known as CHARGE syndrome.

Coronary artery fistula is an uncommon congenital disease that requires invasive treatment for symptomatic patients.

There is a congenital disease called cretinism which essentially is due to a lack of thyroid secretion.

Adverse events continue to be the major challenge, especially among the young critically ill children with complex congenital disease.

Mutations responsible for inherited disease may act by disrupting normal transcriptional splicing.

Cystic fibrosis is the most common life-threatening inherited disease in Ireland.

Cystic fibrosis is Ireland's most common life-threatening genetically inherited disease.

So Tessie Wartliz was suffering from an inherited disease commonly called "Greed."

Fanconi anemia (FA) is a recessive inherited disease characterized by defective DNA repair.

The couple's eldest daughter Taya did not suffer from the inherited disorder.

The inherited disorder limits the blood's ability to carry oxygen throughout the body.

Charcot-Marie-Tooth disease is the most common inherited disorder of the peripheral nervous system.

Here, we resolve the genetic basis of this recessively inherited disorder.

The inherited disorder causes cumulative severe damage to the lungs.

I have a hereditary condition called Stickler Syndrome.

The discovery of the underlying gene could be helpful for the understanding of this heterogeneous hereditary condition.

Albinism is a rare, hereditary condition that leads to a lack of pigmentation in the hair, skin and eyes.

The first is caused by a hereditary condition which causes the body to absorb too much iron from the digestive system.

His autopsy found the Olympique Lyonnais player suffered from hypertrophic cardiomyopathy, a hereditary condition which increases the risk of collapse during exercise.