Introduction: Waardenburg's syndrome is a rare inherited disorder of congenital hearing loss and Pigmentary disturbances of the eyes, hair, skin and neural crest derivatives. Methodology: 620 students in a deaf/blind school were examined and four had Waardenburg's syndrome with a frequency of 0.65%. 2 males and 2 females with Waardenburg's syndrome and age ranges between 10-19years (mean 15.75years) All 4 subjects had complete blue irides, white forelock and sensorineural hearing loss, and thus met the diagnostic criteria. They were then subjected to Audiometric assessment. Results: Otoscopy was essentially normal but Audiometry revealed sensorineural hearing loss [SNHL] in all the subjects ranging from severe to profound with one subject b...
Background/Objectives: North- Eastern Nigeria lies within the meningitis belt of sub-Saharan Africa,...
Waardenburg syndrome is a rare genetic disorder with at least 1,400 cases has been reported in medic...
Objective: (a) To report computed tomography findings of eight new cases with Waardenburg's syndrome...
This report is about ocular and audiometric findings in three children with Waardenburg syndrome Typ...
Background: Waardenburg syndrome (WS) is a rare hereditary disorder essentially characterised by dea...
Aim: Waardenburg syndrome is a very rare condition, inherited autosomally with genetic heterogeneity...
Waardenburg's Syndrome {WS} is described in two girls of a Nigerian family. Both girls presented wit...
A six year old boy presented with delay in acquiring language skills. Examination revealed heterochr...
WOS: 000237311700005PubMed: 16719276Waardenburg syndrome in the Turkish deaf population: Waardenburg...
Waardenburg syndrome (WS) is a rare genetic disorder characterized by hearing loss (HL) and pigment ...
Introduction: The most relevant clinical symptom in Waardenburg syndrome is profound bilateral senso...
To determine the visual characteristics of Japanese subjects with the Waardenburg syndrome type 2. M...
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, ...
Objective: Waardenburg syndrome is a rare disease characterized by sensorineural deafness in associa...
Background/Objectives: North- Eastern Nigeria lies within the meningitis belt of sub-Saharan Africa,...
Waardenburg syndrome is a rare genetic disorder with at least 1,400 cases has been reported in medic...
Objective: (a) To report computed tomography findings of eight new cases with Waardenburg's syndrome...
This report is about ocular and audiometric findings in three children with Waardenburg syndrome Typ...
Background: Waardenburg syndrome (WS) is a rare hereditary disorder essentially characterised by dea...
Aim: Waardenburg syndrome is a very rare condition, inherited autosomally with genetic heterogeneity...
Waardenburg's Syndrome {WS} is described in two girls of a Nigerian family. Both girls presented wit...
A six year old boy presented with delay in acquiring language skills. Examination revealed heterochr...
WOS: 000237311700005PubMed: 16719276Waardenburg syndrome in the Turkish deaf population: Waardenburg...
Waardenburg syndrome (WS) is a rare genetic disorder characterized by hearing loss (HL) and pigment ...
Introduction: The most relevant clinical symptom in Waardenburg syndrome is profound bilateral senso...
To determine the visual characteristics of Japanese subjects with the Waardenburg syndrome type 2. M...
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, ...
Objective: Waardenburg syndrome is a rare disease characterized by sensorineural deafness in associa...
Background/Objectives: North- Eastern Nigeria lies within the meningitis belt of sub-Saharan Africa,...
Waardenburg syndrome is a rare genetic disorder with at least 1,400 cases has been reported in medic...
Objective: (a) To report computed tomography findings of eight new cases with Waardenburg's syndrome...