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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Main Authors: Iti Varshney (Author), Mohammad Adil (Author), Syed Suhail Amin (Author), Mohd Mohtashim (Author), Annu Priya (Author), Mahtab Alam (Author)
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出版: Termedia Publishing House, 2020-06-01T00:00:00Z.
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3rd Floor Main Library

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索引號: A1234.567
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