Ring chromosome 10

From WikiMD's WELLNESSPEDIA

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]

NIH info on Ring chromosome 10

Ring chromosome 10 is a rare disease.

Rare and genetic diseases

Rare diseases - Ring chromosome 10

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Also see	* Comprehensive list of genetic and rare diseases
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

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