It is feasible that the major title of the record Chromosome 22 Ring is not the name you expected. Kindly examine the basic synonyms specifying to locate the alternate name(s) and also disorder community(s) covered by this record.
- Ring 22
- Ring 22, Chromosome
Chromosome 22 Ring is a rare condition defined by irregularities of the 22nd chromosome. Associated signs as well as searchings for could be incredibly variable from case to instance. Nevertheless, the disorder is usually associated with modest to serious mental deficiency. Some impacted individuals might likewise have fairly moderate, nonspecific physical (i.e., dysplastic) functions, whereas others might have much more distinctive, potentially extreme physical problems. Baseding on reports in the medical literature, usual searchings for consist of lessened muscle tissue tone (hypotonia) and also electric motor incoordination; an unsteady manner of walking (gait); pronounced spoken hold-ups; and/or certain malformations of the skull and face (craniofacial) area. Such craniofacial irregularities might include an abnormally tiny head (microcephaly); vertical skin folds that might cover the eyes’ inner edges (epicanthal folds up); uncommonly huge ears; and/or various other malformations. Chromosome 22 Ring is usually dued to spontaneous or “de novo” errors quite early in the property development of the embryo that show up to take place arbitrarily for unidentified factors.