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 source]

Ring chromosome 10 is a rare disease.

Ring chromosome 10 Resources
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Rare diseases - Ring chromosome 10
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Resources	NIH GARD, US Genetic and Rare Diseases Info Rare Disease Day Undiagnosed Diseases Network Database of rare diseases at Orphanet Rare Disease UK Rare diseases search engine