PROGERIA SYNDROME: FTI'S Approaches For Progeria Syndrome Clinical Trials Case Reports Year wise Events - Couverture souple

Dave, Vivek; Paliwal, Dr.Sarvesh; Kr.Vishwakarma, Pushpendra

 
9783639322101: PROGERIA SYNDROME: FTI'S Approaches For Progeria Syndrome Clinical Trials Case Reports Year wise Events
Couverture souple
ISBN 10 : 363932210X ISBN 13 : 9783639322101
Editeur : VDM Verlag Dr. Müller, 2010

Synopsis

Progeria (also known as "Hutchinson?Gilford progeria syndrome" and "Hutchinson?Gilford syndrome") is an extremely rare, severe, genetic condition wherein symptoms resembling aspects of aging are manifested at an early age. The disease has a very low incidence and occurs in one per eight million live births.Those born with progeria typically live about thirteen years, although many have been known to live into their late teens and early twenties and rare individuals may even reach their forties. It is a genetic condition that occurs as a new mutation and is not usually inherited, although there is a uniquely inheritable form. This is in contrast to another rare but similar premature aging syndrome, dyskeratosis congenita (DKC), which is inheritable and will often be expressed multiple times in a family line.

Les informations fournies dans la section « Synopsis » peuvent faire référence à une autre édition de ce titre.

Présentation de l'éditeur

Progeria (also known as "Hutchinson?Gilford progeria syndrome" and "Hutchinson?Gilford syndrome") is an extremely rare, severe, genetic condition wherein symptoms resembling aspects of aging are manifested at an early age. The disease has a very low incidence and occurs in one per eight million live births.Those born with progeria typically live about thirteen years, although many have been known to live into their late teens and early twenties and rare individuals may even reach their forties. It is a genetic condition that occurs as a new mutation and is not usually inherited, although there is a uniquely inheritable form. This is in contrast to another rare but similar premature aging syndrome, dyskeratosis congenita (DKC), which is inheritable and will often be expressed multiple times in a family line.

Biographie de l'auteur

Vivek Dave have done M.Pharm in Pharmaceutics from manipal college of pharmaceutical sciences,India. He is perusing Ph.D. from Banasthali University, Jaipur, India. His research interest in delivery of various drugs through transdermal, nanoparticle&ocular route.

Les informations fournies dans la section « A propos du livre » peuvent faire référence à une autre édition de ce titre.

Éditeur
VDM Verlag Dr. Müller
Date d'édition
2010
Langue
anglais
ISBN 10 
363932210X
ISBN 13 
9783639322101
Reliure
Broché
Nombre de pages
172
Coordonnées du fabricant
non disponible
Personne responsable
non disponible