Ring Chromosome 13 in a Filipino Child– A new category with new features?
DOI:
https://doi.org/10.47895/amp.v42i2.2395Keywords:
13 chromosome
developmental delay
facial dysmorphism
genital abnormality
vertebral abnormalities
hypotonia
joint laxity
Abstract
We report on a child with ring chromosome 13 syndrome whose main clinical manifestations coincide with those of previously described cases. However, additional features such as marked hypotonia and joint laxity were noted in this child, anomalies which have not been previously reported in individuals with ring 13.