Seckel syndrome: A case report of the rare syndrome

Seckel syndrome: A case report of the rare syndrome

Seckel syndrome is a rare genetic disorder characterized by marked intra-uterine growth retardation (primordial dwarfism) and post natal dwarfism, microcephaly, mental retardation and typical facial features with a 'bird-headed' appearance. The syndrome has autosomal recessive inheritance...

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Bibliographic Details
Main Authors: N Mahesh, Sivan Sathish, Lakshmayya Naidu, Sanjay Reddy, J Rajesh K. Reddy, Pavan Kancherla
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2018-01-01
Series:Journal of Dr. NTR University of Health Sciences
Subjects:
Apertognathia
“Bird - like” facies
micrognathia
mental retardation
Online Access:http://www.jdrntruhs.org/article.asp?issn=2277-8632;year=2018;volume=7;issue=3;spage=223;epage=227;aulast=Mahesh

Internet

http://www.jdrntruhs.org/article.asp?issn=2277-8632;year=2018;volume=7;issue=3;spage=223;epage=227;aulast=Mahesh

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