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Chromosome 10 ring syndrome: A rare chromosomal disorder where genetic material from one or both ends of chromosome 10 is missing and the two broken ends have rejoined to form a ring. The resulting type and severity of symptoms is determined by the amount and location of genetic material missing. More detailed information about the symptoms, causes, and treatments of Chromosome 10 ring syndrome is available below.
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Prognosis for Chromosome 10 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.
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A syndrome in which both ends of chromosome 10 have been lost (deletion) and the two broken ends have reunited to form a ring-shaped figure. Psychomotor retardation, craniofacial abnormalities (mainly microcephaly and eye and nose deformities), hypoplastic male genitalia, transverse palmar creases, and occasional heart anomalies are the usual abnormalities. - (Source - Diseases Database)
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