Seckel syndrome: A report of a case

Seckel syndrome, first defined by Seckel in 1960, is a rare (incidence 1:10,000), genetically heterogeneous autosomal recessive disorder presenting at birth. This syndrome is characterized by a proportionate dwarfism of prenatal onset, a severe microcephaly with a "bird-headed" like appear...

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Bibliographic Details
Main Authors: K Ramalingam, S D Kaliyamurthy, M Govindarajan, S Swathi
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2012-01-01
Series:Journal of Indian Society of Pedodontics and Preventive Dentistry
Subjects:
Online Access:http://www.jisppd.com/article.asp?issn=0970-4388;year=2012;volume=30;issue=3;spage=258;epage=261;aulast=Ramalingam