Sentences with phrase «genetic bone disease»

New preclinical research provides support to a drug that has been repurposed to possibly treat a rare and extremely disabling genetic bone disease, particularly in children.

Researchers have developed a new way to study bone disorders and bone growth, using stem cells from patients afflicted with a rare, genetic bone disease.

My son Phoenix had a rare genetic bone disease called Osteogenesis Imperfecta Type 2.

In 2015, we got our first exclusive contract with a pharmaceutical company that makes an enzyme replacement therapy for hypophosphatasia, which is a genetic bone disease where babies are born without this specific enzyme.

Research interests include cartilage and joint diseases such as osteoarthritis, rheumatoid arthritis, osteoporosis, bone tumors, and genetic bone diseases including chondrodysplasia

Not exact matches

The 59 - year - old, who was the first full - time wheelchair user to be voted into Westminster, was born with Gauchers Disease, a genetic condition that causes bones to break easily.

A rare genetic disease leaves its victims debilitated by transforming soft tissue cells into bone cells, creating a strange second skeleton.

Clinically, the genetic and trauma - caused conditions are very similar, with bone formation in muscle leading to pain and restricted movement, according to the leader of the new study, Edward Hsiao, MD, PhD, an endocrinologist who cares for patients with rare and unusual bone diseases at the UCSF Metabolic Bone Clinic in the Division of Endocrinology and Metabolbone formation in muscle leading to pain and restricted movement, according to the leader of the new study, Edward Hsiao, MD, PhD, an endocrinologist who cares for patients with rare and unusual bone diseases at the UCSF Metabolic Bone Clinic in the Division of Endocrinology and Metabolbone diseases at the UCSF Metabolic Bone Clinic in the Division of Endocrinology and MetabolBone Clinic in the Division of Endocrinology and Metabolism.

Researchers at the National Institutes of Health worked with 15 patients from around the world to uncover a genetic basis of «dripping candle wax» bone disease.

Fibrodysplasia ossificans progressive (FOP) is a rare, but devastating genetic disease where bone is grown within soft tissue, such as skeletal muscle.

«Drug candidate stops extra bone growth in animal model of rare, genetic disease.»

Another risk posed by short stature is that it can trigger other diseases, such as bone dysplasias, congenital heart disease, asthma or diabetes and genetic disorders such as Turner's or Down syndrome, hypothyroidism and growth hormone deficiency.

The most important advancement in medicine in the last 25 years was the development of genetic modeling in animals, enabling us to figure out how fundamental mechanisms of physiology and disease work, such as in bone loss.

Hosts infected by viruses found new uses for the genetic material the agents of disease left behind; metabolic enzymes somehow came to refract light rays through the eye's lens; mammals took advantage of the sutures between the skull bones to help their young pass through the birth canal; and, in the signature example, feathers appeared in fossils before the ancestors of modern birds took to the skies.

FOP is one of the most rare genetic diseases known, occurring in about one in two million people, but spontaneous bone development is relatively common in the broader population.

inherited neurodegenerative disorders, an array of other genetic diseases, and multiple cancers of the bone marrow and lymph nodes.

Now, in a study recently published in the journal PLOS ONE, a team of scientists from VCU Massey Cancer Center have shown a genetic relationship between the reactivation of hCMV and the onset of graft - versus - host disease (GVHD), a potentially deadly condition in which the immune system attacks healthy tissue following a bone marrow or stem cell transplant.

As a result, local Azeris suffer cancer rates 22 to 51 percent higher than their countrymen and their children suffer from a host of genetic defects ranging from mental retardation to bone diseases.

These models allow genetic dissection of calcification which is to relevant to many diseases like atherosclerosis, gout, stone and bone formation.

Rare genetic diseases like LFS are good study models because they tend to proceed from a change in a single gene, as opposed to many, overlapping changes seen in more related common diseases, in this case more common, non-inherited bone cancers.

«This model, when combined with a rare genetic disease, revealed for the first time how a protein known to prevent tumor growth in most cases, p53, may instead drive bone cancer when genetic changes cause too much of it to be made in the wrong place.»

This extremely rare genetic disease causes muscle, tendons, and ligaments to turn into bone, earning it the nickname «stone man syndrome.»

Bone diseases, either genetic (X-linked hypophosphatemia) or dietary (rickets), represent an essential failure of the bone cell secretory system to maintain a stable calcium phosphate - mineralized collagen scaffBone diseases, either genetic (X-linked hypophosphatemia) or dietary (rickets), represent an essential failure of the bone cell secretory system to maintain a stable calcium phosphate - mineralized collagen scaffbone cell secretory system to maintain a stable calcium phosphate - mineralized collagen scaffold.

Bethesda, MD (Scicasts)- Researchers at the National Institutes of Health worked with 15 patients from around the world to uncover a genetic basis of «dripping candle wax» bone disease.

A genetic screening approach to studying bone disease has found nine new genes associated with bone health and suggests a...

A genetic screening approach to studying bone disease has found nine new genes associated with bone health and suggests a new way to discover genes that may be implicated in human skeletal diseases.

But other rare genetic variants can protect one from heart disease or AIDS, or can lead to unusually strong bones or muscles.

• Increase energy, performance, and stamina • Strengthen the immune system • Lower most risk factors for cardiovascular disease • Improve brain function: mood, intelligence, behavior, and vision • Aid in weight reduction • Regulate organs and glands • Speed recovery and healing • Support healthy child development • Improve digestion • Decrease infection • Keep bones strong • Protect genetic material • Ease PMS • Produces beautiful skin, hair, and nails

However, long - term studies on the effects of fluoride are showing that it can cause a multitude of health issues including cancer (specifically bladder), gum disease, thyroid dysfunction, kidney and liver disease, genetic defects, endocrine imbalance, nervous system disorders and bone disease including fluorosis.

Orthopaedic Nursing: It includes treating people with musculoskeletal diseases, namely broken bones, arthritis, fractures, osteoporosis, and genetic malformations.

There are many causes of anemia, including excessive blood loss due to trauma, immune - mediated diseases (when the body attacks its own cells or organs), cancer, genetic defects, kidney disease (or diseases in the other major organs), infectious diseases and bone marrow disease.

We are all born with a pattern which shapes our bodies, from eye, hair, and skin color, to height, bone structure, longevity, and of course, any predisposition towards genetic diseases but...

Legg - Perthes Disease Another condition that has a strong genetic component, Legg - Perthes causes the tip of the femur (the thigh bone) to degenerate.