30
Jun
Ring chromosome 20 syndrome: genetics, clinical characteristics, and overlapping phenotypes
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Ring chromosome 20 syndrome – the genetics of inheritance and the main symptom: seizures. Ring autosomes are relatively rare, but ring chromosome 20 may be the most common type of all autosomal rings. Based on the analysis of the literature and their own experience, the authors showed that ring chromosome... Read More
22
Jul
Delayed Neuropsychomotor Development and Seizures in a Patient with Ring Chromosome 20 – Candidate Genes
Delayed Neuropsychomotor Development and Seizures in a Patient with Ring Chromosome 20 – Candidate Genes Ring chromosomes are rare chromosomal abnormalities in which the long arm of the chromosome has been fused with the short arm. This often results in deletions and duplications of the chromosome. Ring Chromosome 20... Read More
