Chromosome 22

Common Name(s)

Chromosome 22

Description for this condition is not yet available.
 

Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Chromosome 22" for support, advocacy or research.

Chromosome 22 Central

Our mission is to provide support and information to families or individuals affected by disorders of chromosome 22.

Last Updated: 11 May 2014

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General Support Organizations

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Chromosome 22" for support, advocacy or research.

Chromosome 22 Central

Our mission is to provide support and information to families or individuals affected by disorders of chromosome 22.

http://www.c22c.org

Last Updated: 11 May 2014

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General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Chromosome 22" returned 171 free, full-text research articles on human participants. First 3 results:

Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p11.22→q11.21::) in an 18-year-old female with short stature, obesity, attention deficit hyperactivity disorder, and intellectual disability.
 

Author(s): Chih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chien-Wen Yang, Meng-Shan Lee, Wayseen Wang

Journal: Taiwan J Obstet Gynecol. 2016 Dec;55(6):856-860.

 

We present molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome (sSMC) derived from chromosome 8.

Last Updated: 31 Dec 1969

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Proptosis, Micrognathia, Low Set Ear and Chest Deformity in a Patient with Extra Marker Chromosome 22.
 

Author(s): Asieh Mosallanejad, Fatemeh Sayarifard, Sima Hosseinverdi, Farzaneh Abbasi, Hosein Shabni Mirzaee, Nima Rezaei

Journal: Acta Med Iran. 2015 Dec;53(12):782-4.

 

There is a number of syndromes, associated with proptosis, micrognathia, low-set ear and chest deformity. Herein, we report a 9-year-old female with such phenotype who was presented with a vaginal neuroma. The result of karyotype showed 47XX, with extra marker chromosome 22. Although ...

Last Updated: 31 Dec 1969

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B-cell Acute Lymphoblastic Leukemia With t(9;22)(q34;q11) Translocation and Clonal Divergence Through ider(22) Chromosome and t(13;17)(q14;q25) Translocation.
 

Author(s): Juan Pablo Meza-Espinoza, Enrique Jhonatan Romo Martínez, Lilia Aguilar López, Verónica Judith Picos Cárdenas, María Teresa Magaña Torres, Juan Ramón González García

Journal: Ann Lab Med. 2016 Mar;36(2):185-7.

 

Last Updated: 31 Dec 1969

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Reviews from the PubMed Database

Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Chromosome 22" returned 3 free, full-text review articles on human participants. First 3 results:

Constitutional rearrangements of chromosome 22 as a cause of neurofibromatosis 2.
 

Author(s): T Tsilchorozidou, F H Menko, F Lalloo, A Kidd, R De Silva, H Thomas, P Smith, A Malcolmson, J Dore, K Madan, A Brown, J G Yovos, M Tsaligopoulos, N Vogiatzis, M E Baser, A J Wallace, D G R Evans

Journal: J. Med. Genet.. 2004 Jul;41(7):529-34.

 

Last Updated: 31 Dec 1969

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Partial trisomy of chromosome 22 resulting from an interstitial duplication of 22q11.2 in a child with typical cat eye syndrome.
 

Author(s): M Meins, P Burfeind, S Motsch, R Trappe, D Bartmus, S Langer, M R Speicher, H Mühlendyck, I Bartels, B Zoll

Journal: J. Med. Genet.. 2003 May;40(5):e62.

 

Last Updated: 31 Dec 1969

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Human chromosome 22.
 

Author(s): J C Kaplan, A Aurias, C Julier, M Prieur, M F Szajnert

Journal: J. Med. Genet.. 1987 Feb;24(2):65-78.

 

The acrocentric chromosome 22, one of the shortest human chromosomes, carries about 52 000 kb of DNA. The short arm is made up essentially of heterochromatin and, as in other acrocentric chromosomes, it contains ribosomal RNA genes. Ten identified genes have been assigned to the long ...

Last Updated: 31 Dec 1969

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Clinical Trial Information This information is provided by ClinicalTrials.gov

Study of Inotuzumab Ozogamicin Combined to Chemotherapy in Older Patients With Philadelphia Chromosome-negative CD22+ B-cell Precursor ALL
 

Status: Not yet recruiting

Condition Summary: Acute Lymphoblastic Leukemia (ALL) - Philadelphia Chromosome (Ph)-Negative CD22+ B-cell Precursor (BCP)

 

Last Updated: 10 Aug 2017

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Non-Invasive Chromosomal Evaluation of 22q11.2
 

Status: Recruiting

Condition Summary: DiGeorge Syndrome, Velocardiofacial Syndrome, 22q.11.2 Deletion Syndrome

 

Last Updated: 15 Jul 2016

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