The disease occurs when a unique kind of cell invades the lungs and causes tissue destruction by creating holes or cysts in the lung. It can be fatal and the just known treatment is usually a lung transplant. To date, LAM provides been expensive and hard to diagnose, usually requiring a biopsy or high resolution CT scan. Due to low awareness of LAM, the first symptoms are mistaken for other respiratory conditions such as asthma often, bronchitis or emphysema. The availability of this non-invasive diagnostic check might eliminate the dependence on a surgical lung biopsy to diagnose LAM, significantly improving the standard of life in ladies who could be suspected LAM sufferers. It will be helpful in screening for LAM in women with TSC, a genetic disorder that causes tumours to form in lots of different organs.Obtained Orphan Drug Designation from the FDA for PRX-8066, a selective serotonin 2B receptor antagonist, in Phase II development for pulmonary arterial hypertension Received two grants totaling nearly $0.5 million for research and development efforts linked to Viibryd and Stedivaze Reported a cash burn for the quarter of $4.7 million, including $6.0 million related to a portion of the cash arises from the sale of the Company’s genetic testing business, $1.5 million from the release of funds held in escrow from a earlier deal, and other items totaling approximately $1.0 million Related StoriesTesting amniotic fluid could guide doctors to create delivery planning decisions for preterm birthsGenetic reduction of AMPK enzyme can prevent or delay hearing lossUCSF-led experts map out melanoma's genetic trajectoriesCommenting on the business’s third quarter financial outcomes, Mr.