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Chromosome 7 ring syndrome: A rare chromosomal disorder where the ends of chromosome 7 have been deleted and the two broken ends have rejoined to form a ring shape resulting in a range of symptoms determined by the size of the genetic deletion. More detailed information about the symptoms, causes, and treatments of Chromosome 7 ring syndrome is available below.
See full list of 32 symptoms of Chromosome 7 ring syndrome
Read more about treatments for Chromosome 7 ring syndrome
Read more about causes of Chromosome 7 ring syndrome.
Research the causes of these diseases that are similar to, or related to, Chromosome 7 ring syndrome:
Prognosis for Chromosome 7 ring syndrome: 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 7 ring syndrome
Types of Chromosome 7 ring syndrome
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An anomaly in which two ends of chromosome 7 have been lost (deletion) and the two broken ends have reunited to form a ring-shaped figure. The syndrome is rare and is characterized mainly by brain anomalies, microcephaly, midfacial dysplasia, mental deficiency, dermatological abnormalities, growth failure, cleft lip and palate, genital deformities, and other variable defects. - (Source - Diseases Database)
Chromosome 7 ring syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Chromosome 7 ring syndrome, or a subtype of Chromosome 7 ring syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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