Search on: BOURNEVILLE DISEASE 
Descriptors Found: 1
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Descriptor English:   Tuberous Sclerosis 
Descriptor Spanish:   Esclerosis Tuberosa 
Descriptor Portuguese:   Esclerose Tuberosa 
Synonyms English:   Bourneville Disease
Epiloia
Phakomatosis, Bourneville  
Tree Number:   C04.445.810
C10.500.507.875
C10.562.850
C10.574.500.865
C16.131.666.507.875
C16.320.400.880
Definition English:   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) 
Allowable Qualifiers English:  
BL blood CF cerebrospinal fluid
CI chemically induced CL classification
CO complications DI diagnosis
DH diet therapy DT drug therapy
EC economics EM embryology
EN enzymology EP epidemiology
EH ethnology ET etiology
GE genetics HI history
IM immunology ME metabolism
MI microbiology MO mortality
NU nursing PS parasitology
PA pathology PP physiopathology
PC prevention & control PX psychology
RA radiography RI radionuclide imaging
RT radiotherapy RH rehabilitation
SU surgery TH therapy
US ultrasonography UR urine
VE veterinary VI virology
Record Number:   14804 
Unique Identifier:   D014402 

Occurrence in VHL:
 

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