Add to ORKGAbstract: Waardenburg 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
WOS: 000222302200006PubMed ID: 15029423Background. Waardenburg syndrome (WS) is an autosomal dominan...
Waardenburg syndrome (WS) is a rare genetic disorder characterized by hearing loss (HL) and pigment ...
Objectives: Sensorineural hearing impairment (HI) is one of the most frequent congenital defects, wi...
Waardenburg syndrome is an inherited disease characterized by sensorineural hearing loss, pigmen-tat...
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...
Aim: Waardenburg syndrome is a very rare condition, inherited autosomally with genetic heterogeneity...
Waardenburg syndrome is a rare disease characterized by sensorineural deafness in association with p...
Introduction: Waardenburg's syndrome is a rare inherited disorder of congenital hearing loss and Pig...
Waardenburg's Syndrome {WS} is described in two girls of a Nigerian family. Both girls presented wit...
Waardenburg syndrome (WS), first described by Dutch ophthalmologist PJ Waardenburg, is a congenital ...
Waardenburg Syndrome is a rare disorder of neural crest cell development. It is genetically inherite...
Waardenburg syndrome is a rare genetic disorder with at least 1,400 cases has been reported in medic...
Waadernburg syndrome (WS) is an autosomal dominant disease clinically and genetically heterogeneous....
PubMed ID: 15029423Background. Waardenburg syndrome (WS) is an autosomal dominant disorder character...
WOS: 000222302200006PubMed ID: 15029423Background. Waardenburg syndrome (WS) is an autosomal dominan...
Waardenburg syndrome (WS) is a rare genetic disorder characterized by hearing loss (HL) and pigment ...
Objectives: Sensorineural hearing impairment (HI) is one of the most frequent congenital defects, wi...
Waardenburg syndrome is an inherited disease characterized by sensorineural hearing loss, pigmen-tat...
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...
Aim: Waardenburg syndrome is a very rare condition, inherited autosomally with genetic heterogeneity...
Waardenburg syndrome is a rare disease characterized by sensorineural deafness in association with p...
Introduction: Waardenburg's syndrome is a rare inherited disorder of congenital hearing loss and Pig...
Waardenburg's Syndrome {WS} is described in two girls of a Nigerian family. Both girls presented wit...
Waardenburg syndrome (WS), first described by Dutch ophthalmologist PJ Waardenburg, is a congenital ...
Waardenburg Syndrome is a rare disorder of neural crest cell development. It is genetically inherite...
Waardenburg syndrome is a rare genetic disorder with at least 1,400 cases has been reported in medic...
Waadernburg syndrome (WS) is an autosomal dominant disease clinically and genetically heterogeneous....
PubMed ID: 15029423Background. Waardenburg syndrome (WS) is an autosomal dominant disorder character...
WOS: 000222302200006PubMed ID: 15029423Background. Waardenburg syndrome (WS) is an autosomal dominan...
Waardenburg syndrome (WS) is a rare genetic disorder characterized by hearing loss (HL) and pigment ...
Objectives: Sensorineural hearing impairment (HI) is one of the most frequent congenital defects, wi...