Seckel syndrome associated with oligodontia, microdontia, enamel hypoplasia, delayed eruption, and dentin dysmineralization: A new variant?

Journal of Oral Pathology and Medicine

Volumn 35, Issue 10, 2006, Pages 639-641

  De Coster, P J ^a,b   Verbeeck, R M H ^b   Holthaus, V ^c   Martens, L C ^b   Vral, A ^b  

^a GHENT UNIVERSITY HOSPITAL   (Belgium)

^b GHENT UNIVERSITY   (Belgium)

^c NONE

Author keywords

Dentin dysmineralization; Histology; Microdontia; Seckel syndrome; Tooth agenesis

Indexed keywords

ADOLESCENT; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CASE REPORT; DENTIN; ENAMEL HYPOPLASIA; GROWTH RETARDATION; HUMAN; HYPODONTIA; HYPOPLASIA; MALE; MENTAL DEFICIENCY; OLIGODONTIA; PACHYGYRIA; PHENOTYPE; POSTNATAL GROWTH; PRIORITY JOURNAL; SECKEL SYNDROME;

ABNORMALITIES, MULTIPLE; ADOLESCENT; ANODONTIA; DENTAL ENAMEL HYPOPLASIA; DENTIN; DWARFISM; FACIES; HUMANS; MALE; PHENOTYPE; SYNDROME; TOOTH DEMINERALIZATION; TOOTH ERUPTION;

EID: 33749532322     PISSN: 09042512     EISSN: 16000714     Source Type: Journal    
DOI: 10.1111/j.1600-0714.2006.00462.x     Document Type: Article

References (5)

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