Medications

FDA OKs first treatment for rare genetic disorder

The Food and Drug Administration on Friday approved the first treatment for children and adults with spinal muscular atrophy, a rare genetic disorder marked by progressive muscle weakness that's the most common genetic cause ...

Medical research

A new key in fighting Kennedy's disease

If a disease affects motoneurons, cells that control voluntary muscle activity, researchers should focus their efforts on motoneurons to find potential treatments, right?

Pediatrics

The dying child: Room for improvement in end-of-life care

Many pediatricians and pediatric subspecialists believe that their clinical care extends from treating ill children through end-of-life care. However, are pediatricians actually meeting the needs of families and their dying ...

Medical research

Research breakthrough in fight against muscle wasting diseases

It is estimated that half of all cancer patients suffer from a muscle wasting syndrome called cachexia. Cancer cachexia impairs quality of life and response to therapy, which increases morbidity and mortality of cancer patients. ...

Surgery

Atrophy seen in gluteus maximus post gluteal augmentation

(HealthDay)—The gluteus maximus muscle presents atrophy after gluteal augmentation surgery with implants, according to a study published in the March issue of Plastic and Reconstructive Surgery.

page 5 from 10