1p36 Deletion Syndrome
Common Name(s)
1p36 Deletion Syndrome, Chromosome 1p36 Deletion Syndrome
Advocacy and Support Organizations
Condition Specific Organizations
Following organizations serve the condition "1p36 Deletion Syndrome" for support, advocacy or research.
Our mission is to inform, support and alleviate the isolation of anyone affected by a rare chromosome disorder and to raise public awareness.
Our mission is to help individuals affected by chromosome 1p36 abnormalities overcome the obstacles they face to be able to lead healthy, happy and productive lives. We do this by providing support and education to their families and increasing awareness of chromosome 1p36 abnormalities in the public and medical communities.
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 "1p36 Deletion Syndrome" for support, advocacy or research.
Our mission is to inform, support and alleviate the isolation of anyone affected by a rare chromosome disorder and to raise public awareness.
http://www.rarechromo.org Our mission is to help individuals affected by chromosome 1p36 abnormalities overcome the obstacles they face to be able to lead healthy, happy and productive lives. We do this by providing support and education to their families and increasing awareness of chromosome 1p36 abnormalities in the public and medical communities.
http://www.1p36dsa.org/Recommended Apps
Anonymously share and see how your answers compare with others with this condition while privately providing key pieces of information to medical researchers, disease advocacy groups, and others ONLY YOU select to help speed up cures and better alternatives.
Finding the right clinical trial for 1p36 Deletion Syndrome can be challenging. However, with TrialsFinder (which uses the Reg4ALL database and privacy controls by Private Access), you can permit researchers to let you know opportunities to consider - all without revealing your identity.
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 "1p36 Deletion Syndrome" returned 11 free, full-text research articles on human participants.
First 3 results:
Journal: Methodist Debakey Cardiovasc J. ;10(4):258-9.
Journal:
Deletion of the subtelomeric region of 1p36 is one of the most common subtelomeric deletion syndromes. In monosomy 1p36, the presence of obesity is poorly defined, and glucose metabolism deficiency is rarely reported. However, the presence of a typical Prader-Willi-like phenotype ...
Journal: Am. J. Hum. Genet.. 2014 Jan;94(1):153-4.
To view other free, full-text articles on human participants, please click on the link below.
Reviews from the PubMed Database
Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "1p36 Deletion Syndrome" returned 2 free, full-text review articles on human participants.
First 3 results:
Journal: Rev Chil Pediatr. ;87(5):411-421.
The Monosomy 1p36 deletion syndrome is part of the group of diseases known as Rare Diseases. The objective of the present work is to review the characteristics of Monosomy 1p36 deletion syndrome. The monosomy 1p36 deletion syndrome phenotype includes: dysmorphic craniofacial features; ...
Journal:
The major clinical features of monosomy 1p36 deletion are developmental delay and hypotonia associated with short stature and craniofacial dysmorphisms. The objective of this study was to review the cases of 1p36 deletion that was reported between 1999 and 2014, in order to identify ...
To view other free, full-text review articles on human participants, please click on the link below.
Symptoms, Diagnosis, and Treatment
https://ghr.nlm.nih.gov/condition/22q112-deletion-syndrome
https://ghr.nlm.nih.gov/condition/22q133-deletion-syndrome
https://ghr.nlm.nih.gov/condition/proximal-18q-deletion-syndrome
https://ghr.nlm.nih.gov/condition/19p1313-deletion-syndrome
https://ghr.nlm.nih.gov/condition/jacobsen-syndrome
https://ghr.nlm.nih.gov/condition/distal-18q-deletion-syndrome
https://ghr.nlm.nih.gov/condition/2q37-deletion-syndrome
https://ghr.nlm.nih.gov/condition/kleefstra-syndrome
https://ghr.nlm.nih.gov/condition/3p-deletion-syndrome
https://ghr.nlm.nih.gov/condition/3q29-microdeletion-syndrome
https://ghr.nlm.nih.gov/condition/1q211-microdeletion
https://ghr.nlm.nih.gov/chromosome/1
https://ghr.nlm.nih.gov/gene/KIF1B
https://ghr.nlm.nih.gov/condition/16p112-deletion-syndrome
https://ghr.nlm.nih.gov/condition/17q12-deletion-syndrome
https://ghr.nlm.nih.gov/condition/9q223-microdeletion
https://ghr.nlm.nih.gov/condition/potocki-shaffer-syndrome
https://ghr.nlm.nih.gov/condition/satb2-associated-syndrome
https://ghr.nlm.nih.gov/condition/smith-magenis-syndrome
There are currently no related results available in GeneReviews.
Clinical Trial Information This information is provided by ClinicalTrials.gov
Condition Summary: 22q11 Deletion Syndrome; DiGeorge Syndrome; Trisomy 21; Trisomy 18; Trisomy 13; Monosomy X; Sex Chromosome Abnormalities; Cri-du-Chat Syndrome; Angelman Syndrome; Prader-Willi Syndrome; 1p36 Deletion Syndrome
Finding the right clinical trial for 1p36 Deletion Syndrome can be challenging. However, with TrialsFinder (which uses the Reg4ALL database and privacy controls by Private Access), you can permit researchers to let you know opportunities to consider - all without revealing your identity.