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Deletion 10pter: A very rare syndrome caused by a chromosomal defect (10p terminal deletion) and can result in a variety of malformations that are similar to DiGeorge syndrome and velocardiofacial syndrome. More detailed information about the symptoms, causes, and treatments of Deletion 10pter is available below.
See full list of 34 symptoms of Deletion 10pter
Read more about treatments for Deletion 10pter
Review possible medical complications related to Deletion 10pter:
Read more about causes of Deletion 10pter.
Prognosis for Deletion 10pter: The prognosis varies depending on the type and severity of symptoms that develop. Prompt diagnosis and appropriate treatment can improve prognosis and quality of life.
More about prognosis of Deletion 10pter
Types of Deletion 10pter
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Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Deletion 10pter as a "rare disease".
Source - Orphanet
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