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Seckel syndrome: a rare case report.

Authors :
Sisodia R
Raj RK
Goel V
Source :
Journal of the Indian Society of Pedodontics and Preventive Dentistry [J Indian Soc Pedod Prev Dent] 2014 Apr-Jun; Vol. 32 (2), pp. 160-3.
Publication Year :
2014

Abstract

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.

Details

Language :
English
ISSN :
1998-3905
Volume :
32
Issue :
2
Database :
MEDLINE
Journal :
Journal of the Indian Society of Pedodontics and Preventive Dentistry
Publication Type :
Academic Journal
Accession number :
24739918
Full Text :
https://doi.org/10.4103/0970-4388.130983