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
The heå loss is present from birth (congenital). Here we present 2 case reports who presented to our outpatient department with the heå loss since birth.
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
In this report a case has been discussed of finding a 30 years old male patient with. Waardenburg syndrome. Keywords: Waardenburg syndrome, autosomal dominant ...
Purpose: Waardenburg syndrome type 1 (WS1) is a rare genetic disorder characterized by dystopia canthorum, abnormal iris pigmentation, and congenital hearing ...
Neural tube defects in Waardenburg syndrome: A case report and review of the literature. ... 2023, INDIAN JOURNAL OF APPLIED RESEARCH, p. 64-65. Crossref ...
Mar 30, 2023 · Waardenburg syndrome is a rare genetically inherited disorder well-known for its classical auditory-pigmentary abnormalities.
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 -
Waardenburg syndrome (WS) is an autosomal disorder with genetic heterogeneity and not all of it forms are dominantly inherited. It is characterised by dystopia ...