It is possible that the primary title of the record Chromosome 21 Ring is not the name you anticipated. Please inspect the synonyms noting to discover the alternative name(s) and disorder subdivision(s) covered by this record.
- Ring 21
- Ring 21, Chromosome
Chromosome 21 Ring is an uncommon chromosomal condition in which the impacted infant has a wreckage of chromosome 21 at both ends, as well as completions of the chromosome collaborate to develop a ring. The quantity of hereditary product lost at both ends of the chromosome might vary. As a result, a baby with hardly any missing genetic product could have no evident signs and symptoms while an infant with a significant part of the chromosomal ends missing could have several signs. When signs of the condition are present, the influenced baby may have dementia in addition to problems of the face, eyes, skeleton, and/or internal body organs.