Progeria in siblings: A rare case report

• Päätekijät: R Sowmiya (Tekijä), D Prabhavathy (Tekijä), S Jayakumar (Tekijä)
• Aineistotyyppi: Kirja
• Julkaistu: Wolters Kluwer Medknow Publications, 2011-01-01T00:00:00Z.
• Aiheet: article
• Linkit: Connect to this object online.

Progeria, also known as Hutchinson-Gilford syndrome, is an extremely rare, severe genetic condition wherein symptoms resembling aspects of aging are manifested at an early age. It is an autosomal dominant disorder. It is not seen in siblings of affected children although there are very few case repo...