1p36 Deletion Syndrome

1p36 deletion syndrome (also known as monosomy 1p36) is a congenital genetic disorder characterized by moderate to severe intellectual disability, delayed growth, hypotonia, seizures, limited speech ability, malformations, hearing and vision impairment, and distinct facial features. The symptoms may vary, depending on the exact location of the chromosomal deletion.

The condition is caused by a genetic deletion (loss of a segment of DNA) on the outermost band on the short arm (p) of chromosome 1. It is one of the most common deletion syndromes. It is estimated that the syndrome occurs in one in every 5,000 to 10,000 births. Knowledge of the disorder has increased a great deal over the last decade, mainly because more patients have been accurately diagnosed and described in international medical literature.

Read more about 1p36 Deletion SyndromeCharacteristics, History, Genetics, Treatments and Therapy

Other articles related to "1p36 deletion syndrome, 1p36, 1p36 deletion":

1p36 Deletion Syndrome - Treatments and Therapy
... Although 1p36 Deletion Syndrome can be debilitating in many ways, patients do respond to various treatments and therapies ... American Sign Language Because few individuals with Monosomy 1p36 develop complex speech, an alternate form of communication is critical to development ... Music Music has been shown to aid children with 1p36 deletion in various developmental areas ...

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