Hutchinson-Gilford progeria syndrome: a rare premature ageing syndrome
Hutchinson-Gilford progeria syndrome is an extremely rare genetic disorder characterized by premature ageing involving the skin, bones, heart, and blood vessels. The incidence is 1 in several million births. It occurs sporadically and is probably an autosomal dominant syndrome. The diagnosis is esse...
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Termedia Publishing House,
2020-06-01T00:00:00Z.
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A1234.567 |
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