Seckel syndrome: A rare case report

Sisidia, Rinky and K.S., Ravi and Goel, Vipin (2014) Seckel syndrome: A rare case report. Working Paper. Medknow Publications.

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Official URL | رابط موقع المجلة: http://www.jisppd.com/article.asp?issn=0970-4388;y...

Abstract|ملخص البحث

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. KEYWORDS: Bird-headed appearance, dwarfi sm, microcephaly, seckel syndrome

Item Type|تصنيف النتاج العلمي: Monograph |دراسةعلمية تخصصية (Working Paper)
Subjects | مجال موضوع النشر: Dentistry
Divisions | الكلية: College of Dentistry > Dentistry
Depositing User: ravi raj
Date Deposited: 23 Oct 2018 05:02
Last Modified: 23 Oct 2018 05:02
URI: http://eprints.kku.edu.sa/id/eprint/2624

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