Your question: What is the function of chromosome 6?

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What happens if you are missing chromosome 6?

Features that often occur in people with chromosome 6q deletion include developmental delay , intellectual disability , and distinctive facial features. Most cases are not inherited , but people can pass the deletion on to their children. Treatment is based on the signs and symptoms present in each person.

What disease is associated with chromosome 6?

Ring chromosome 6 syndrome is a rare chromosomal anomaly syndrome with highly variable phenotype principally characterized by prenatal/postnatal growth failure, intellectual disability , developmental delay , craniofacial dysmorphism (incl.

How common is chromosome 6 deletion?

Chromosome 6p deletions are rare events within the population. At present, there are 43 cases in the medical literature, excluding ring chromosome 6 anomalies.

How many genes are there on chromosome 6?

Chromosome 6 likely contains 1,000 to 1,100 genes that provide instructions for making proteins.

What does partial trisomy mean?

Chromosome 6, Partial Trisomy 6q is an extremely rare chromosomal disorder in which a portion of the 6th chromosome (6q) is present three times (trisomy) rather than twice in cells of the body. Associated symptoms and findings may vary in range and severity from case to case.

What chromosome is affected by MS?

Multiple Sclerosis Gene Cluster Pinpointed. Sept. 28, 2005 (San Diego) — The most comprehensive genetic study to date of multiple sclerosis has pinpointed a cluster of genes on chromosome 6 as playing the major role in causing the disorder.

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What does Cri du Chat mean?

Cri du chat syndrome is a rare genetic disorder caused by missing pieces on a particular chromosome. It is not the result of anything the parents have done or failed to do. The characteristics of a newborn with cri du chat syndrome include a high-pitched cry, a small head and a flattened bridge of the nose.