Like most other chromosome disorders, this increases the risk of birth defects, developmental delay and learning difficulties. Olivia Farnsworth has a rare chromosome condition - a chromosome 6 deletion - that has left medics and her family stunned. Olivia Farnsworth, a 10 years girl , represents an extremely rare case of chromosome 6 deletion . The severity of the condition and the signs and symptoms depend on the size and location of the deletion … Olivia first grabbed the attention of doctors when the girl's mother brought her to hospital after the child was hit by a car. She is believed to be he only person in the world to … And she is from Huddersfield. 5p-Deletion. While she sounds like a character on “Heroes.” her doctors say Olivia is one of only 100 people in the world with a “chromosome 6 deletion.” That means her chromosome 6 (out of 46) is missing, which causes one or more of the conditions she has – no feelings of pain, hunger or exhaustion. Doctors diagnosed she had a problem with the deletion of chromosome 6. Two copies of chromosome 6, one copy inherited from each parent, form one of the pairs. Chromosome 6 Ring is a rare disorder in which there is loss (deletion) of chromosomal material from both ends of the 6th chromosome and joining of the ends to form a ring. Changes to chromosome 6 may include deletions or duplications of genetic material in the short (p) or long (q) arm of the chromosome in each cell, or a circular structure called ring chromosome 6. Identifying genes on each chromosome is an active area of genetic research. Chromosome 6q deletion is a chromosome abnormality that occurs when there is a missing copy of the genetic material located on the long arm (q) of chromosome 6. She can’t feel hunger, exhausted and discomfort because of chromosome 6 deletion. Doctors say this is due to deletion of chromosome 6: the girl lacks part of the genetic information which should have been present in her, Gazeta reports, citing The Daily mail. Due to chromosome 6 deletion, she cannot feel hungry, tired and pain. Doctors diagnosed that she has a chromosome 6 deletion issue. It is a rare kind of genetical disorder. What this means in simple terms is that a part of chromosome 6 has been wiped out between sections 13 and 14.2. And this abnormally is as a result of a congenital condition in which the chromosome is deleted during the process of cell division. Olivia Farnsworth, seven, from Huddersfield, has a rare condition described as chromosome 6 deletion. Chromosome 6p deletion case of Olivia is unique and only case in the world. In 2016 she was hit by a car and dragged 30 meters, yet felt nothing and emerged with minor injuries. In future, we can hope that Non-oxygen depended GMO can be created. the story begun when Olivia was hit by a car and she just stood up and walked without shedding a single tear . On March 8, three days after her third birthday, test results confirmed that Katy suffers from a deletion on chromosome 6. Chromosome 6q Deletion Syndrome is a chromosome abnormality that occurs when there is a missing copy of the genetic material located on the long arm (q) of chromosome 6 The severity of the condition and the signs and symptoms depend on the size and location of the deletion … Chromosome 6 spans about 171 million DNA building blocks (base pairs) and represents between 5.5 and 6 percent of the total DNA in cells.