Search on: BRANCHIO-OTORENAL DYSPLASIA 
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Descriptor English:   Branchio-Oto-Renal Syndrome 
Descriptor Spanish:   Síndrome Branquio Oto Renal 
Descriptor Portuguese:   Síndrome Brânquio-Otorrenal 
Synonyms English:   Branchio-Oculo-Facial Syndrome
Branchio-Otorenal Dysplasia
BOR Syndrome  
Tree Number:   C16.131.077.208
C16.131.260.090
C16.320.180.090
Definition English:   An autosomal dominant disorder manifested by various combinations of preauricular pits, branchial fistulae or cysts, lacrimal duct stenosis, hearing loss, structural defects of the outer, middle, or inner ear, and renal dysplasia. Associated defects include asthenic habitus, long narrow facies, constricted palate, deep overbite, and myopia. Hearing loss may be due to Mondini type cochlear defect and stapes fixation. (Jablonski's Dictionary of Syndromes & Eponymic Diseases, 2d ed) 
History Note English:   97 
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:   32954 
Unique Identifier:   D019280 

Occurrence in VHL:
 

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