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Syndrome in question
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نویسنده
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peruzzo j. ,nazar f.l. ,tubone m.q. ,escobar g.f. ,cestari t.f.
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منبع
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journal brazilian annals of dermatology - 2015 - دوره : 90 - شماره : 4 - صفحه:589 -590
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چکیده
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Waardenburg 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. © 2015 by anais brasileiros de dermatologia.
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کلیدواژه
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Deafness; Genetic; Genetic diseases; Inborn; Skin diseases; Waardenburg syndrome
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آدرس
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federal university of rio grande do sul (ufrgs),porto alegre,rs, Brazil, federal university of rio grande do sul (ufrgs),porto alegre,rs, Brazil, private clinic,porto alegre,rs, Brazil, federal university of rio grande do sul (ufrgs),porto alegre,rs, Brazil, federal university of rio grande do sul (ufrgs),porto alegre,rs, Brazil
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Authors
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