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Chromosome 1 ring: A rare chromosomal disorder where the ends of chromosome 1 are deleted and the chromosome rejoins to form a ring. The disorder is characterized by mental and physical development delay, short stature and low birth weight. More detailed information about the symptoms, causes, and treatments of Chromosome 1 ring is available below.
See full list of 6 symptoms of Chromosome 1 ring
Read more about treatments for Chromosome 1 ring
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Read more about causes of Chromosome 1 ring.
Research the causes of these diseases that are similar to, or related to, Chromosome 1 ring:
Prognosis for Chromosome 1 ring: 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 Chromosome 1 ring
Read about other experiences, ask a question about Chromosome 1 ring, or answer someone else's question, on our message boards:
Chromosome 1 ring is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Chromosome 1 ring, or a subtype of Chromosome 1 ring,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Chromosome 1 ring as a "rare disease".
Source - Orphanet
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