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Seckel syndrome: a rare case report.
- 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.
- Subjects :
- Child
Humans
Male
Syndrome
Abnormalities, Multiple physiopathology
Subjects
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