Waardenburg syndrome (WS) is a uncommon autosomal inherited and genetically heterogenous disorder .Patients have heterochromia or eyes with iris of different ...
CASE REPORT. A 16 days old male babypresented with complains of not passing stools and bilious vomiting since birth,abdominal distension since 10.
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.
Pawar A,. Dimri U.. Indian. Journal of. Applied. Research. 2017 https://www.worldwidejournals.com/ indian-journal-of-applied-research-. (IJAR)/article/ ...
Atrichia with papular lesions is a rare Autosomal recessive disorder characterized clinically by complete and irreversible hair loss shortly after birth.
Aim: This study aims at studying different congenital ocular and its adnexal anomalies over a period of two years in a tertiary care hospital and their ...
Oct 22, 2024 · Background: Waardenburg syndrome is a group of rare genetic conditions. ... We report a unique case of seven siblings with Waardenburg syndrome.
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The Centre for Cellular & Molecular Biology (CCMB) is a premier research organization in frontier areas of modern biology. The objectives of the Centre are ...
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: ...