Jacobsen syndrome

From Simple English Wikipedia, the free encyclopedia

Jacobsen syndrome (also known as 11q deletion syndrome) is a gene mutation caused by the deletion of certain genes on chromosome 11.[1] The number of deleted genes can be anywhere from 5 million to 16 million pairs of DNA. The effects of Jacobsen include brain development issues, unique facial features, and often a bleeding disorder called the Paris-Trousseau syndrome.

References[change | change source]

  1. Reference, Genetics Home. "Jacobsensyndrome". Genetics Home Reference.