Add to ORKGWaardenburg syndrome is an inherited disease characterized by sensorineural hearing loss, pigmen-tation 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
Objectives: Sensorineural hearing impairment (HI) is one of the most frequent congenital defects, wi...
Waardenburg's Syndrome {WS} is described in two girls of a Nigerian family. Both girls presented wit...
Waardenburg syndrome (WS) is a rare genetic disorder characterized by hearing loss (HL) and pigment ...
Waardenburg syndrome is an inherited disease characterized by sensorineural hearing loss, pigmen-tat...
Abstract: Waardenburg syndrome is an inherited disease characterized by sensorineural hearing loss, ...
Aim: Waardenburg syndrome is a very rare condition, inherited autosomally with genetic heterogeneity...
A six year old boy presented with delay in acquiring language skills. Examination revealed heterochr...
Objective: Waardenburg syndrome is a rare disease characterized by sensorineural deafness in associa...
Background: Waardenburg syndrome (WS) is a rare hereditary disorder essentially characterised by dea...
Waardenburg syndrome (WS), first described by Dutch ophthalmologist PJ Waardenburg, is a congenital ...
Waardenburg syndrome is a rare disease characterized by sensorineural deafness in association with p...
Background: Waardenburg syndrome (WS) is a rare, autosomal dominant disorder characterized by conge...
Waardenburg syndrome is a rare genetic disorder with at least 1,400 cases has been reported in medic...
Waardenburg Syndrome is a rare disorder of neural crest cell development. It is genetically inherite...
Abstract Background Waardenburg syndrome is a group of rare genetic conditions. It is determined by ...
Objectives: Sensorineural hearing impairment (HI) is one of the most frequent congenital defects, wi...
Waardenburg's Syndrome {WS} is described in two girls of a Nigerian family. Both girls presented wit...
Waardenburg syndrome (WS) is a rare genetic disorder characterized by hearing loss (HL) and pigment ...
Waardenburg syndrome is an inherited disease characterized by sensorineural hearing loss, pigmen-tat...
Abstract: Waardenburg syndrome is an inherited disease characterized by sensorineural hearing loss, ...
Aim: Waardenburg syndrome is a very rare condition, inherited autosomally with genetic heterogeneity...
A six year old boy presented with delay in acquiring language skills. Examination revealed heterochr...
Objective: Waardenburg syndrome is a rare disease characterized by sensorineural deafness in associa...
Background: Waardenburg syndrome (WS) is a rare hereditary disorder essentially characterised by dea...
Waardenburg syndrome (WS), first described by Dutch ophthalmologist PJ Waardenburg, is a congenital ...
Waardenburg syndrome is a rare disease characterized by sensorineural deafness in association with p...
Background: Waardenburg syndrome (WS) is a rare, autosomal dominant disorder characterized by conge...
Waardenburg syndrome is a rare genetic disorder with at least 1,400 cases has been reported in medic...
Waardenburg Syndrome is a rare disorder of neural crest cell development. It is genetically inherite...
Abstract Background Waardenburg syndrome is a group of rare genetic conditions. It is determined by ...
Objectives: Sensorineural hearing impairment (HI) is one of the most frequent congenital defects, wi...
Waardenburg's Syndrome {WS} is described in two girls of a Nigerian family. Both girls presented wit...
Waardenburg syndrome (WS) is a rare genetic disorder characterized by hearing loss (HL) and pigment ...