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Monosomy 1p36: A rare chromosomal disorder where deletion of a portion of chromosome 1 causes various abnormalities such as heart problems, mental retardation, developmental delay, facial dysmorphism and short stature. The range and severity of symptoms is variable with some cases being relatively mild. More detailed information about the symptoms, causes, and treatments of Monosomy 1p36 is available below.
See full list of 58 symptoms of Monosomy 1p36
See full list of 10 treatments for Monosomy 1p36
Review possible medical complications related to Monosomy 1p36:
Read more about causes of Monosomy 1p36.
Prognosis for Monosomy 1p36: The prognosis varies considerably 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 Monosomy 1p36
Types of Monosomy 1p36
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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 Monosomy 1p36 as a "rare disease".
Source - Orphanet
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