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Psychology and Mental Health Dictionary Definitions - Chromosome 1p36 Deletion Syndrome - Psychforums.com





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Chromosome 1p36 Deletion Syndrome


Chromosome 1p36 Deletion Syndrome is categorized as a rare disease. Chromosome 1p36 Deletion Syndrome is a rare genetic disorder caused by the genetic deletion on the outermost band on the short arm of chromosome 1. Opposite of a chromosome duplication. This disease is the result of a loss or a mutation of genetic material of a chromosome. Chromosome 1p36 Deletion Syndrome as a syndrome, reflects a set of signs and symptoms that in most cases occur together and which indicates increased chances of developing a particular disease or already the presence of it. If you suffer from a rare disease like this one, if you want to know more information about this illness, you want to share your problems or you seek for support, check our dedicated forum about rare diseases where issues about Chromosome 1p36 Deletion Syndrome are discussed (discussions about treatments, medications, pathology, signs, symptoms of Chromosome 1p36 Deletion Syndrome, etc...).
For more informations on Chromosome 1p36 Deletion Syndrome check our rare disease forum.

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