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Jacobsen syndrome is a condition characterized by the deletion of several genes on chromosome 11. Signs and symptoms vary among affected people but often include Paris-Trousseau syndrome (a bleeding disorder); distinctive facial features; delayed development of motor skills and speech; and cognitive impairment.
Jul 9, 2017 · Jacobsen syndrome is a rare genetic disorder caused by the deletion of genes in chromosome 11. It can result in birth defects, learning disabilities, bleeding disorders, and other complications.
Jacobsen syndrome is a genetic condition caused by a deletion of chromosome 11 material. It affects development, behavior, facial features, bleeding, and other systems.
Jacobsen syndrome is a rare chromosomal disorder resulting from deletion of genes from chromosome 11 that includes band 11q24.1. It is a congenital disorder. Since the deletion takes place on the q arm of chromosome 11, it is also called 11q terminal deletion disorder. [1]
Jacobsen syndrome is a genetic disorder caused by the loss of genes from the end of chromosome 11. It affects the development of the face, heart, limbs and brain, and can vary in severity depending on the size and location of the deletion.
Jacobsen syndrome is a contiguous gene disorder caused by deletions in the long arm of chromosome 11, affecting craniofacial, cardiac, hematological, renal and immunological systems. Learn about its epidemiology, clinical description, diagnosis, management, prognosis and resources.
Aug 2, 2023 · Jacobsen syndrome is a condition caused by a loss (deletion) of genetic material from chromosome 11. Because this deletion most commonly occurs at the end (terminus) of the long (q) arm of chromosome 11, Jacobsen syndrome is also known as 11q terminal deletion disorder.
