Family with low-grade neuroendocrine carcinoma of salivary glands, severe sensorineural hearing loss, and enamel hypoplasia

American Journal of Medical Genetics

Volumn 83, Issue 3, 1999, Pages 183-186

  Michaels, L ^a,e   Lee, K ^b   Manuja, S L ^c   Soucek, S O ^d  

^a ROYAL NATIONAL THROAT NOSE AND EAR HOSPITAL   (United Kingdom)

^b UNIVERSITY OF LONDON   (United Kingdom)

^c Department of Medicine   (United Kingdom)

^d ST MARY S HOSPITAL   (United Kingdom)

^e ROYAL FREE AND UNIVERSITY COLLEGE MEDICAL SCHOOL   (United Kingdom)

Author keywords

Amelogenesis imperfecta; Hereditary sensorineural hearing loss; Neuroendocrine carcinoma; Salivary gland neoplasia

Indexed keywords

ADULT; AGED; ARTICLE; CLINICAL ARTICLE; ENAMEL HYPOPLASIA; FEMALE; HEARING LOSS; HUMAN; MALE; NEUROENDOCRINE TUMOR; PEDIGREE ANALYSIS; PERCEPTION DEAFNESS; PRIORITY JOURNAL; SALIVARY GLAND CARCINOMA; TOOTH DEVELOPMENT; TOOTH DISEASE;

ADOLESCENT; ADULT; AGED; CARCINOMA, NEUROENDOCRINE; CHILD; DENTAL ENAMEL HYPOPLASIA; FEMALE; HEARING LOSS, SENSORINEURAL; HUMANS; IMMUNOHISTOCHEMISTRY; LINKAGE (GENETICS); MALE; MICROSCOPY, ELECTRON; MIDDLE AGED; PEDIGREE; SALIVARY GLAND NEOPLASMS; X CHROMOSOME;

RAPHIA FRATER;

EID: 0033582937     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19990319)83:3<183::AID-AJMG7>3.0.CO;2-2     Document Type: Article

References (3)

1. Karrman C, Backman B, Dixon M, Holmgrcn G, Forsman K. 1997. Mapping of the locus for autosomal dominant amelogenesis imperfecta (AIH2) to a 4-MB YAC contigon chromosome 4qll- q21. Genomics 39: 164-170.
2. Lagerstrom M, Dahl N, Nakahori Y, Nakagome Y, Backman B, Landegren U, Pettersson U. 1991. A deletion in the amelogenin gene (AMG) causes X-linked amelogenesis imperfecta. Genomics 10:971-975.
3. Witkop CJ Jr. 1988. Amelogenesis imperfecta, dentinogenesis imperfecta and dentin dysplasia revisited: problems in classification. J Oral Pathol 17:547-553.