Search on: BRANCHIO-OCULO-FACIAL SYNDROME 
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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) 
Indexing Annotation English:   multiple abnorm; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES; DF: note short X ref
History Note English:   97 
Allowable Qualifiers English:  
blood cerebrospinal fluid
chemically induced classification
complications diet therapy
diagnosis drug therapy
economics ethnology
embryology enzymology
epidemiology etiology
genetics history
immunology metabolism
microbiology mortality
nursing pathology
prevention & control physiopathology
parasitology psychology
radiography rehabilitation
radionuclide imaging radiotherapy
surgery therapy
ultrastructure urine
ultrasonography veterinary
virology  
Record Number:   32954 
Unique Identifier:   D019280 

Occurrence in VHL:
 

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