Ring chromosome 10
Other Names: Chromosome 10 ring; Ring 10; R10
An autosomal anomaly characterized by variable clinical features, depending on the size and precise location of deleted chromosome segments. Most patients present with developmental delay, intellectual disability,growth retardation, microcephaly, clinodactyly, and dysmorphic features. Congenital heart disease and genitourinary anomalies were reported in some cases.
NIH genetic and rare disease info[edit]
Ring chromosome 10 is a rare disease.
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Rare diseases - Ring chromosome 10
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