The bald can now take heart: a new research has identified a gene associated with loss of hair that could, in turn, lead to new drugs to treat baldness.
                                           The particular gene has been blamed                                            for a rare hereditary form of hair                                            loss called hypotrichosis simplex – a                                            condition that affects 1 in 200,000                                            people.
                                          Those suffering from hypotrichosis                                            simplex start getting bald in                                            childhood. 
                                           It was after six years of research                                            that an international team, headed by                                            scientists at the University of Bonn,                                            Germany, succeeded in identifying the                                          
                                          gene hypotrichosis simplex that is                                            responsible for the rare hereditary                                            form of hair loss. 
This is the first research of its kind to identify a receptor that plays a role in hair growth and hair loss.
A healthy person loses about 100 hairs a day, which is not a problem provided the lost hairs are replaced and the losses occur evenly around the head. However, when hair loss goes beyond this point, it can become a problem for those affected, particularly a psychological one.
The condition affects both men and women. The sufferers usually begin going bald in childhood and the process of hair loss advances with age.
                                           In the new study, reported in the                                            journal Nature Genetics, Regina Betz,                                            of the University of Bonn and leader                                            of the study, writes, “There is a very                                            good
                                          chance of developing a therapy to                                            treat hair loss based on this                                            finding.” 
                                           The researchers used DNA samples from                                            11 members of a Saudi Arabian family                                            that had the rare condition and found                                            a mutation in the P2Y5 gene prevented                                            proteins called growth receptors on                                            hair follicle cells from forming                                            properly. The DNA samples helped the                                            researchers to understand some of
                                          the fundamental mechanisms of hair                                            growth and hair loss. 
The study of the samples showed that a substance needed to stimulate hair growth could not attach to the defective receptors and may help explain hair loss, the researchers said. The finding, the researchers added, could also lead to making drugs that could boost hair growth.
They now hope that their will lead to new therapies that could treat various forms of hair loss.
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