Chromosome 9

Common Name(s)

Chromosome 9

Description for this condition is not yet available.
 

Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Chromosome 9" for support, advocacy or research.

Chromosome 9 Disorder Advocates

Changing the world one chromosome and one hope at a time. We are your voice and your direction if ever you feel speechless or lost.

Last Updated: 3 Aug 2016

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General Support Organizations

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How do you compare to others with this condition?

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Chromosome 9" for support, advocacy or research.

Chromosome 9 Disorder Advocates

Changing the world one chromosome and one hope at a time. We are your voice and your direction if ever you feel speechless or lost.

http://www.facebook.com/9qdeletion

Last Updated: 3 Aug 2016

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General Support Organizations

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General Resources

46,XY,del(9)(q31.2q33.1)

Single case chromosome disorder in 9

Updated 27 Nov 2013

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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 9" returned 192 free, full-text research articles on human participants. First 3 results:

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: 28 Dec 2015

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Pericentric Inversion of Human Chromosome 9 Epidemiology Study in Czech Males and Females.
 

Author(s): A Šípek, A Panczak, R Mihalová, L Hrčková, E Suttrová, V Sobotka, P Lonský, N Kaspříková, V Gregor

Journal: Folia Biol. (Praha). 2015 ;61(4):140-6.

 

Pericentric inversion of human chromosome 9 [inv(9)] is a relatively common cytogenetic finding. It is largely considered a clinically insignificant variant of the normal human karyotype. However, numerous studies have suggested its possible association with certain pathologies, e.g., ...

Last Updated: 7 Oct 2015

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Independent Mechanisms Target SMCHD1 to Trimethylated Histone H3 Lysine 9-Modified Chromatin and the Inactive X Chromosome.
 

Author(s): Nicholas J Brideau, Heather Coker, Anne-Valerie Gendrel, C Alistair Siebert, Karel Bezstarosti, Jeroen Demmers, Raymond A Poot, Tatyana B Nesterova, Neil Brockdorff

Journal: Mol. Cell. Biol.. 2015 Dec;35(23):4053-68.

 

The chromosomal protein SMCHD1 plays an important role in epigenetic silencing at diverse loci, including the inactive X chromosome, imprinted genes, and the facioscapulohumeral muscular dystrophy locus. Although homology with canonical SMC family proteins suggests a role in chromosome ...

Last Updated: 31 Oct 2015

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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 9" returned 3 free, full-text review articles on human participants. First 3 results:

Double jeopardy from a single translocation: deletions of the derivative chromosome 9 in chronic myeloid leukemia.
 

Author(s): Brian J P Huntly, Anthony Bench, Anthony R Green

Journal: Blood. 2003 Aug;102(4):1160-8.

 

Chronic myeloid leukemia (CML) is characterized by formation of a BCR-ABL fusion gene, usually as a consequence of the Philadelphia (Ph) translocation between chromosomes 9 and 22. Recently the development of new fluorescence in-situ hybridization (FISH) techniques has allowed identification ...

Last Updated: 5 Aug 2003

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Another patient with an interstitial deletion of chromosome 9: case report and a review of six cases with del(9)(q22q32).
 

Author(s): H Y Kroes, J H Tuerlings, R Hordijk, N R Folkers, L P ten Kate

Journal: J. Med. Genet.. 1994 Feb;31(2):156-8.

 

We report a case of del(9)(q22q32) in a severely mentally retarded boy. The most prominent clinical features are short stature, microcephaly, dysmorphic facies, and delayed bone age. Although six cases of this deletion have now been reported, confirmation of a definite syndrome is not yet possible.

Last Updated: 16 Jun 1994

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Symptoms, Diagnosis, and Treatment

There are currently no related results available in GeneReviews.

There are currently no related results available in Genetic Testing Registry.

 
 
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Clinical Trial Information This information is provided by ClinicalTrials.gov

Understanding Clinical Phenotype and Collecting Biomarker Samples in C9ORF72 ALS
 

Status: Recruiting

Condition Summary: C9ORF72 Amyotrophic Lateral Sclerosis (ALS)

 

Last Updated: 5 Jan 2017

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Nivolumab and Dasatinib in Treating Patients With Relapsed or Refractory Philadelphia Chromosome Positive Acute Lymphoblastic Leukemia
 

Status: Recruiting

Condition Summary: B Acute Lymphoblastic Leukemia With t(9;22)(q34;q11.2); BCR-ABL1; Recurrent Adult Acute Lymphoblastic Leukemia; Recurrent Childhood Acute Lymphoblastic Leukemia; Refractory Adult Acute Lymphoblastic Leukemia; Refractory Childhood Acute Lymphoblastic Leukemia

 

Last Updated: 25 Aug 2016

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Imatinib Mesylate and Combination Chemotherapy in Treating Patients With Newly Diagnosed Philadelphia Chromosome Positive Acute Lymphoblastic Leukemia
 

Status: Not yet recruiting

Condition Summary: B Acute Lymphoblastic Leukemia With t(9;22)(q34.1;q11.2); BCR-ABL1; BCR-ABL1 Fusion Protein Expression; Minimal Residual Disease; Philadelphia Chromosome Positive; T Acute Lymphoblastic Leukemia; Untreated Adult Acute Lymphoblastic Leukemia; Untreated Childhood Acute Lymphoblastic Leukemia

 

Last Updated: 7 Feb 2017

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