Abstract : Waardenburg syndrome (WS) is a uncommon autosomal inherited and genetically heterogenous disorder .Patients have heterochromia or eyes with iris of ...
CASE REPORT. A 16 days old male babypresented with complains of not passing stools and bilious vomiting since birth,abdominal distension since 10.
We report a case of a 14-year-old Romanian male, with a family history of Waardenburg syndrome (mother) and Usher syndrome (father - congenitally sensorineural ...
Neural tube defects in Waardenburg syndrome: A case report and review of the literature. Am J Med Genet A. 2017;173(9):2472–7. https://doi.org/10.1002/ajmg.a.
Waardenburg, P.J.: A New Syndrome Combining De- velopmental Anomalies of the Eyelids, Eyebrows and. Nose Root With Pigmentary Defects of the Iris and. Head ...
The Centre for Cellular & Molecular Biology (CCMB) is a premier research organization in frontier areas of modern biology. The objectives of the Centre are ...
Nov 12, 2022 · Background: Waardenburg syndrome is a group of rare genetic conditions. ... We report a unique case of seven siblings with Waardenburg syndrome.
Diffuse melanotic lesion of the iris as a presenting feature of ciliary body melanocytoma: report of a case and review of the literature. ... 2023, INDIAN JOURNAL ...
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Jan 6, 2022 · Waardenburg Syndrome: Rare Case Report, Original Research. Paper, International Journal Of Scientific Research, 2019(8)2. No. Yes. NO. YES. 13.
isolation of Rhizopus homothallicus from a patient of rhino-orbital cerebral mucormycosis : a rare case report. Indian journal of applied research. 2021, 11;9: ...