Bannayan-Riley-Ruvalcaba syndrome: Report of a family

Oral Diseases

Volumn 7, Issue 5, 2001, Pages 310-314

  Wilson, P H R ^a   MacDonald, D G ^a   Felix, D H ^a  

^a GLASGOW DENTAL HOSPITAL AND SCHOOL   (United Kingdom)

Author keywords

Bannayan Riley Ruvalcaba; Hyperplasia; Oral dysaesthesia; Orofacial; Parosteal fasciitis; Syndrome

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; BANNAYAN RILEY RUVALCABA SYNDROME; CASE REPORT; CLINICAL FEATURE; COWDEN SYNDROME; DENTAL SURGERY; DISEASE ASSOCIATION; FAMILIAL DISEASE; HUMAN; MALE; MOUTH DISEASE; PRIORITY JOURNAL; SCHOOL CHILD;

ABNORMALITIES, MULTIPLE; ADOLESCENT; ADULT; CHILD; CRANIOFACIAL ABNORMALITIES; DIAGNOSIS, DIFFERENTIAL; FAMILY HEALTH; FASCIITIS; GINGIVAL NEOPLASMS; HAMARTOMA SYNDROME, MULTIPLE; HUMANS; HYPERPLASIA; MALE; MOUTH MUCOSA; PALATE, HARD; POLYPS; SYNDROME;

EID: 0035163504     PISSN: 1354523X     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1601-0825.2001.00679.x     Document Type: Article

References (11)

1. Deletion of PTEN in a patient with Bannayan-Riley-Ruvalcaba syndrome suggests allelism with Cowden disease
2. Lipomatosis, angiomatosis and macroencephalia: A previously undescribed congenital syndrome
3. Bannayan-Riley-Ruvalcaba syndrome: Renaming three formerly recognised syndromes as one etiologic entity
4. Cowden's disease: A rare but important manifestation of oral papillomatosis
5. Bannayan-Riley-Ruvalcaba syndrome
6. Cowden syndrome (multiple hamartoma syndrome)
7. PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome
8. Early diagnosis of multiple hamartoma and neoplasia syndrome: The role of the dentist
9. Macrocephaly, pseudopapilloedema and multiple hemangiomata - A previously undescribed heredofamilial syndrome
10. Sotos syndrome with intestinal polyposis and pigmentary changes of the genitalia
11. Oral manifestations in Cowden's syndrome