Syndrome in Question
An. bras. dermatol
;
90(4): 589-590, July-Aug. 2015. tab, ilus
Article
in English
| LILACS
| ID: lil-759211
ABSTRACT
AbstractWaardenburg syndrome is an inherited disease characterized by sensorineural hearing loss, pigmentation changes and minor facial malformations. It has four clinical variants. We report the case of a girl who, like her mother, was affected by this syndrome. The diagnosis was made after detection and treatment of deafness.
Full text:
Available
Index:
LILACS (Americas)
Main subject:
Waardenburg Syndrome
Type of study:
Diagnostic study
/
Screening study
Limits:
Child
/
Female
/
Humans
Language:
English
Journal:
An. bras. dermatol
Journal subject:
Dermatology
Year:
2015
Type:
Article
Affiliation country:
Brazil
Institution/Affiliation country:
Federal University of Rio Grande do Sul/BR
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