Hutchinson-Gilford Progeria Syndrome : A Rare Genetic Disorder
Joint Authors
Bhuyan, Sanat K.
Bhuyan, Ruchi
Panigrahi, Rajat G.
Maragathavalli, G.
Vijayakumar, Poornima
Pati, Abhishek Ranjan
Panigrahi, Antarmayee
Choudhury, Priyadarshini
Source
Issue
Vol. 2013, Issue 2013 (31 Dec. 2013), pp.1-4, 4 p.
Publisher
Hindawi Publishing Corporation
Publication Date
2013-10-30
Country of Publication
Egypt
No. of Pages
4
Main Subjects
Abstract EN
Hutchinson-Gilford progeria syndrome (HGPS) is a rare pediatric genetic syndrome with incidence of one per eight million live births.
The disorder is characterised by premature aging, generally leading to death at approximately 13.4 years of age.
This is a follow-up study of a 9-year-old male with clinical and radiographic features highly suggestive of HGPS and presented here with description of differential diagnosis and dental consideration.
This is the first case report of HGPS which showed pectus carinatum structure of chest.
American Psychological Association (APA)
Panigrahi, Rajat G.& Panigrahi, Antarmayee& Vijayakumar, Poornima& Choudhury, Priyadarshini& Bhuyan, Sanat K.& Bhuyan, Ruchi…[et al.]. 2013. Hutchinson-Gilford Progeria Syndrome : A Rare Genetic Disorder. Case Reports in Dentistry،Vol. 2013, no. 2013, pp.1-4.
https://search.emarefa.net/detail/BIM-486644
Modern Language Association (MLA)
Panigrahi, Rajat G.…[et al.]. Hutchinson-Gilford Progeria Syndrome : A Rare Genetic Disorder. Case Reports in Dentistry No. 2013 (2013), pp.1-4.
https://search.emarefa.net/detail/BIM-486644
American Medical Association (AMA)
Panigrahi, Rajat G.& Panigrahi, Antarmayee& Vijayakumar, Poornima& Choudhury, Priyadarshini& Bhuyan, Sanat K.& Bhuyan, Ruchi…[et al.]. Hutchinson-Gilford Progeria Syndrome : A Rare Genetic Disorder. Case Reports in Dentistry. 2013. Vol. 2013, no. 2013, pp.1-4.
https://search.emarefa.net/detail/BIM-486644
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references
Record ID
BIM-486644
