Extractions: Syndrome Bourneville-Pringle syndrome Synonyms Bourneville disease Bourneville syndrome Bourneville-Brissaud disease Pringle disease adenoma sebaceum epiploia hereditary multiple system hamartomatosis neurinomatosis centralis neuromatosis universalis neurospongioblastosis diffusa phacomatosis sclerosis tuberosa spongioblastosis circumscripta tuberose sclerosis tuberous sclerosis Summary A triad of epilepsy, mental retardation, and angiofibromas of numerous organs with intracranial hamartomatous lesions involving subependymal nodules and cerebral cortical tubers (hence the name "tuberous sclerosis." Major Features Head and neck: Thickened calvaria, exostosis of the frontal bone, and increased density of the cranium occur in most cases. Eyes: Retinal hamartomas occur in about half of all cases Mouth and oral structures: Fibrous growth on oral mucosa and gingiva. Hand and foot: Two thirds of patients exhibit cystlike areas on the phalanges and new bone formation on the metacarpal and metatarsal bones. Large single digit may occur. Extremities: New bone formation may occur on the long bones.
Tuberous Sclerosis Information Diseases Database Tuberous sclerosis bournevillepringle syndrome Bourneville's disease Epiloia, Disease Database Information http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126
Syndrome DB - Table Of Contents bournevillepringle syndrome Brachmann-Cornelia de Lange (BCDL) syndrome (BDLS) brachycephaly-deafness-cataract-microstomia-mental retardation syndrome http://www.nlm.nih.gov/mesh/jablonski/syndrome_toc/toc_b.html
Tuberous Sclerosis Information Diseases Database Tuberous sclerosis,bournevillepringle syndrome,Bourneville s disease,Epiloia,Disease Database Information. http://www.diseasesdatabase.com/ddb13433.htm
Cmj3802 bournevillepringle syndrome Detected at the Age of Two Days. Nikola Susic,Katarina Kapeli, Alenka Miletic-Juric, Zeljko Buric, Jasna Duic http://www.cmj.hr/1997/3802/susic.htm
CMJ - June 1997 (Volume 38, Number 2) bournevillepringle syndrome Detected at the Age of Two Days Nikola Susic, KatarinaKapeli, Alenka Miletic-Juric, Zeljko Buric, Jasna Duic. Correspondence http://www.cmj.hr/1997/3802/contents.htm
Entrez PubMed BACKGROUND/METHODS To present a 26year-old woman affected by the abortive formof Bourneville-Prin http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=1
Entrez PubMed Aside from the classical trias of symptoms, BournevillePringle s syndrome showsa lot of other alte http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=3
BRINT Research Directories 204) Body Dysmorphic Disorder (20) Bone Disorders (1,120) Borderline PersonalityDisorder (58) Botulism (19) bournevillepringle syndrome (15) Bovine http://portal.brint.com/cgi-bin/getit/links/Health/Conditions_and_Diseases/B/
Extractions: An autosomal dominant disorder which is generally classified as a phacomatosis. Pathologically, the condition is characterized by glial cell tumors which arise in the cerebral hemispheres and retina. There is an increased incidence of benign rhabdomyomas of the heart and angiomyolipomas of kidney, liver, lungs, thyroid, and testes. Clinical manifestations include MENTAL RETARDATION; adenoma sebaceum of the face (actually angiofibromas); EPILEPSY; SPASMS; INFANTILE; Shagreen patches on the trunk; and subungual fibromas. (From Adams et al., Principles of Neurology, 6th ed, p1011) Synonyms and Source Vocabularies:
