Hutchinson – Gilford progeria syndrome: A rare case report

Hutchinson – Gilford Progeria Syndrome is a rare genetic disorder characterized by premature aging involving the skin, bones, heart, and blood vessels. We report a three-year-old boy with clinical manifestations characteristic of this syndrome. He had a characteristic “plucked-bird” appearance, prom...

Descripción completa

Detalles Bibliográficos
Autores principales: Kashyap, Subhash, Shanker, Vinay, Sharma, Neeraj
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4228646/
https://www.ncbi.nlm.nih.gov/pubmed/25396134
http://dx.doi.org/10.4103/2229-5178.142507

Ejemplares similares

Ejemplares similares