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Waardenburg syndrome (WS) is a uncommon autosomal inherited and genetically heterogenous disorder .Patients have heterochromia or eyes with iris of different ...
Waardenburg syndrome is a rare genetic disorder characterized by varying degree of deafness associated with pigmentary anomaly and defects of neural crest ...
Missing: IJAR - Applied Research
Here we present 2 case reports who presented to our outpatient department with the heå loss since birth. Audiological evaluation revealed bilateral severe – ...
Waardenburg syndrome (WS) is a rare genetic disorder. Patients have heterochromia or eyes with iris of different color, increased inter-canthal distance, ...
Missing: IJAR - Applied
Dec 15, 2020 · Waardenburg syndrome is a genetic disorder named after a Dutch ophthalmologist who has first described the triad of hearing loss, ...
Neural tube defects in Waardenburg syndrome: A case report and review of the literature. ... 2023, INDIAN JOURNAL OF APPLIED RESEARCH, p. 64-65. Crossref ...
Waardenburg syndrome (WS) is a rare autosomally inherited and genetically heterogeneous disorder of neural crest cell development with distinct cutaneous ...
Missing: IJAR - Applied
Waardenburg syndrome (WS) is a rare genetic disorder characterized by congenital sensorineural hearing loss and pigmentary abnormalities of the hair, skin ...
Missing: IJAR - | Show results with:IJAR -
A rare genetic mutation case report: Waardenburg syndrome type I. Case Report. Author Details : Gagandeep Kaur , Anureet Kaur , Mandeep Kaur* , Haramritpal ...
Missing: IJAR - Applied
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