What this means in simple terms is that a part of chromosome 6 has been wiped out between sections 13 and 14.2. Chromosome 6 Deletions: A chromosome 6 deletion is a rare disorder in which some of the genetic material that makes up one of the bodyâs 46 chromosomes â specifically chromosome 6 in this case â is missing. It is a congenital condition in which some of the parts of chromosome 6 deleted during the process of cell division. Her official karyotype is 46,xx, del (6) q13q14.2. She never feels pain, hunger or fatigue. Olivia Farnsworth is an eleven-year-old British girl, born in Huddersfield, England. Generally, affected individuals do survive well into adult life. Olivia Farnsworth, seven, from Huddersfield, has a rare condition described as chromosome 6 deletion. Olivia Farnsworth, a cute little girl, has baffled the medics by her super human abilities. On March 8, three days after her third birthday, test results confirmed that Katy suffers from a deletion on chromosome 6. My parents were told to expect some delays because she had been in an orphanage for the first 10 months of her life. Olivia Farnsworth, a 10 years girl , represents an extremely rare case of chromosome 6 deletion . Katy's official karyotype is 46,xx, del (6) q13q14.2. This is due to her rare condition of Chromosome 6 Deletion. She is believed to be he only person in the world to exhibit the three symptoms together. Apart from two sex chromosomes (two Xs for a girl and an X and a Y for a boy), chromosomes are numbered 1 to 22, generally from largest to smallest. Features that often occur in people with chromosome 6q deletion ⦠There has been one study to date in which the course of 1p36 deletion syndrome was investigated, with a ⦠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.The severity of the condition and the signs and symptoms depend on the size and location of the deletion and which genes are involved. The severity and nature of signs and symptoms of chromosome 1p36 deletion syndrome varies between affected individuals, so it is difficult to predict the long-term outlook for an individual child. Please read on to find out more about our little girl. the story begun when Olivia was hit by a car and she just stood up and walked without shedding a single tear . Deletions of the long arm of chromosome 6 are rare and are characterized by great clinical variability according to the deletion breakpoint. Like most other chromosome disorders, this increases the risk of birth defects, developmental delay and learning difficulties. An 8-year-old girl is the first unique case of chromosome 6p deletion. What this means in simple terms is that a part of chromosome 6 has been wiped out between sections 13 and 14.2. We report a on 6-year-old girl with a de novo 0.63 Mb deletion on chromosome 6q25.1 who demonstrated multiple congenital anomalies including a ventricular septal defect and an underdeveloped cerebellar vermis. Meet the 10-year-old girl who canât feel pain, hunger or fatigue ... Chromosome 6 Deletion is a congenital condition in which the chromosome is deleted during cell division. her mother also said that â Olivia dose not feel hungry and she could stay for days without sleep , and also she never feels danger â . 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