Oral manifestations of patients with Kenny-Caffey Syndrome

European Journal of Medical Genetics

Volumn 55, Issue 8-9, 2012, Pages 441-445

  Moussaid, Youssra ^a   Griffiths, Didier ^b   Richard, Béatrice ^b   Dieux, Anne ^c   Lemerrer, Martine ^a   Léger, Juliane ^d   Lacombe, Didier ^b   Bailleul Forestier, Isabelle ^e,f  

^a UNIVERSITÉ PARIS DESCARTES   (France)

^b UNIVERSITÉ DE BORDEAUX   (France)

^c LILLE UNIVERSITY HOSPITAL   (France)

^d HÔPITAL ROBERT DEBRÉ   (France)

^e UNIVERSITÉ PAUL SABATIER   (France)

^f UNIVERSITY HOSPITALS LEUVEN   (Belgium)

Author keywords

Dental anomalies; Enamel defects; Kenny Caffey syndrome; Microdontia; Oligodontia; Sanjad Sakati syndrome

Indexed keywords

ADOLESCENT; ADULT; AUTOSOMAL RECESSIVE INHERITANCE; BONE DYSPLASIA; CHILD; CHROMOSOME 1Q; CLINICAL ARTICLE; EYE MALFORMATION; FEMALE; FOOT RADIOGRAPHY; GENE; HUMAN; HYPERPIGMENTATION; HYPOCALCEMIA; HYPODONTIA; KENNY CAFFEY SYNDROME; MALE; MEDICAL LITERATURE; MICROCEPHALY; MICRODONTIA; MICROGNATHIA; MOUTH DISEASE; NOSE MALFORMATION; OLIGODONTIA; OSTEOSCLEROSIS; PANORAMIC RADIOGRAPHY; REVIEW; SCHOOL CHILD; SHORT STATURE; TBCE GENE; TOOTH MALFORMATION;

ABNORMALITIES, MULTIPLE; DWARFISM; FOOT DEFORMITIES, CONGENITAL; HUMANS; HYPEROSTOSIS, CORTICAL, CONGENITAL; HYPOCALCEMIA; PHENOTYPE; TOOTH ABNORMALITIES;

EID: 84864137753     PISSN: 17697212     EISSN: 18780849     Source Type: Journal    
DOI: 10.1016/j.ejmg.2012.03.005     Document Type: Review

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