Jacobsen syndrome is a rare congenital chromosomal disorder caused by the loss of genetic material from the end of the long arm of chromosome 11, and for that reason it is also called 11q terminal deletion disorder. The deleted stretch may span roughly five to sixteen million base pairs, and the more DNA is missing, the more severe the symptoms tend to be. People with the syndrome typically have intellectual disability, delayed development, distinctive facial features and a range of physical problems, including heart defects. A large majority also have Paris-Trousseau syndrome, a bleeding disorder caused by dysfunctional platelets. The condition can be fatal, with children dying in early life from heart complications in some cases. It was first identified by the Danish geneticist Petrea Jacobsen in 1973, in a family with an unbalanced translocation between chromosomes 11 and 21. No cure exists, so care focuses on managing the heart, bleeding, developmental and behavioural problems.
Facts
Classification
ICD-10 ChapterXVII: Congenital Malformations, Deformations and Chromosomal Abnormalities 1 Communicable or Non-communicable First Described Prevalence Band Causative Agent
Causative Agent (category) Sources
1. Orphadata (Orphanet): Orphadata cross-references for ORPHA:2308 Jacobsen syndrome
Orphadata (Orphanet)ICD-10 cross-referenceQuote, ICD-10 cross-reference
"Reference": "Q93.5", "Source": "ICD-10"
View the Source 2. National Cancer Institute (NCI Thesaurus): Jacobsen syndrome - NCI Thesaurus concept C75457
National Cancer Institute (NCI Thesaurus)DefinitionQuote, Definition
A very rare genetic syndrome caused by deletion of the terminal band of chromosome 11.
View the Source 3. Jacobsen syndrome (Wikipedia)
History section
The syndrome was first identified by Danish geneticist Petrea Jacobsen in 1973 and was named after her.
Cause section
Jacobsen syndrome is caused by deletion of genetic material from the long arm of chromosome 11.
View the Source4. Orphadata (Orphanet): Orphadata: Epidemiology of rare diseases (en_product9_prev)
Orphadata (Orphanet)ORPHA:2308Quote, ORPHA:2308
Prevalence at birth Value and class 1-9 / 100 000
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