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...

Full description

Saved in:
Bibliographic Details
Main Authors: Iti Varshney (Author), Mohammad Adil (Author), Syed Suhail Amin (Author), Mohd Mohtashim (Author), Annu Priya (Author), Mahtab Alam (Author)
Format: Book
Published: Termedia Publishing House, 2020-06-01T00:00:00Z.
Subjects:
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!

Internet

Connect to this object online.

3rd Floor Main Library

Holdings details from 3rd Floor Main Library
Call Number: A1234.567
Copy 1 Available