Dentinogenesis imperfecta associated with short stature, hearing loss and mental retardation: A new syndrome with autosomal recessive inheritance?

Journal of Oral Pathology and Medicine

Volumn 34, Issue 7, 2005, Pages 444-446

  Cauwels, Rita G E C ^a,b   De Coster, P J ^a   Mortier, G R ^b   Marks, L A M ^a   Martens, L C ^a  

^a GHENT UNIVERSITY   (Belgium)

^b GHENT UNIVERSITY HOSPITAL   (Belgium)

Author keywords

Autosomal recessive; Collagen I; Consanguinity; Dentinogenesis imperfecta

Indexed keywords

COLLAGEN TYPE 1; COLLAGEN TYPE 3; RETICULIN;

ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; BONE RADIOGRAPHY; CASE REPORT; CHILD; CONSANGUINEOUS MARRIAGE; DENTIN; FACIES; FOLLOW UP; GENETIC HETEROGENEITY; HISTOPATHOLOGY; HUMAN; MALE; MENTAL DEFICIENCY; MOLAR TOOTH; OSTEOPOROSIS; PERCEPTION DEAFNESS; PRIORITY JOURNAL; SHORT STATURE; SIBLING; TOOTH COLOR; TOOTH ERUPTION; TOOTH MALFORMATION; TOOTH RADIOGRAPHY;

BODY HEIGHT; CHILD; CHILD, PRESCHOOL; CONSANGUINITY; DENTINOGENESIS IMPERFECTA; GENES, RECESSIVE; HEARING LOSS; HUMANS; MALE; MENTAL RETARDATION; SYNDROME;

EID: 22344455931     PISSN: 09042512     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1600-0714.2005.00318.x     Document Type: Article

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