Seckel syndrome: A rare case report

Seckel syndrome (SS) is a rare, autosomal recessive syndrome; characterized by severe intrauterine and postnatal growth retardation, microcephaly, mental retardation, and typical facial appearance with beaklike protrusion of the midface (bird headed). In addition to the characteristic craniofacial d...

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Bibliographic Details
Main Authors: Rinky Sisodia (Author), Ravi Kadur Sundar Raj (Author), Vipin Goel (Author)
Format: Book
Published: Wolters Kluwer Medknow Publications, 2014-01-01T00:00:00Z.
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100 1 0 |a Rinky Sisodia  |e author 
700 1 0 |a Ravi Kadur Sundar Raj  |e author 
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245 0 0 |a Seckel syndrome: A rare case report 
260 |b Wolters Kluwer Medknow Publications,   |c 2014-01-01T00:00:00Z. 
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500 |a 10.4103/0970-4388.130983 
520 |a Seckel syndrome (SS) is a rare, autosomal recessive syndrome; characterized by severe intrauterine and postnatal growth retardation, microcephaly, mental retardation, and typical facial appearance with beaklike protrusion of the midface (bird headed). In addition to the characteristic craniofacial dysmorphism and skeletal defects, abnormalities have been described in the cardiovascular, hematopoietic, endocrine, gastrointestinal, and central nervous systems. Usually such patients have poor psychomotor development. This case report presents an 8-year-old child with SS born to parents, exposed in Bhopal gas disaster. 
546 |a EN 
690 |a Bird-headed appearance 
690 |a dwarfism 
690 |a microcephaly 
690 |a seckel syndrome 
690 |a Dentistry 
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655 7 |a article  |2 local 
786 0 |n Journal of Indian Society of Pedodontics and Preventive Dentistry, Vol 32, Iss 2, Pp 160-163 (2014) 
787 0 |n http://www.jisppd.com/article.asp?issn=0970-4388;year=2014;volume=32;issue=2;spage=160;epage=163;aulast=Sisodia 
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787 0 |n https://doaj.org/toc/1998-3905 
856 4 1 |u https://doaj.org/article/fa4fb65b58d74a288dcdd8a741ceea00  |z Connect to this object online.