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Ajila, Vidya
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Dentistry

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A Rare Intraoral Manifestation of Nevus of Ota - A Case Report Nair, Mithula; Castelino, Renita L; Ajila, Vidya; Babu, Subhas G; Ghosh, Rumela
Journal of Dentistry Indonesia Vol. 23, No. 3
Publisher : UI Scholars Hub

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Nevus of Ota is a dermal melanocytic nevus which is characterized by benign hamartomatous hyperpigmentation. Clinically it presents as a congenital or acquired blue or gray patch on the face and is distributed on the ophthalmic, maxillary, and mandibular branches of the trigeminal nerve. It is most commonly found in Japanese populations and is rare in the Indian subcontinent. It affects only 0.014 – 0.034% of the Asian population and is less common in the male population, with a male to female ratio of 1.4:8. The involvement of pigmentation over the pinna of the ear and the oral mucosa is extremely rare with very few cases reported in scientific literature. The case reported here is a case of nevus of Ota, with a rare intraoral presentation on the hard palate, crossing the midline.
Binder’s Syndrome – An Unusual Craniofacial Anomaly Madiyal, Ananya; Babu, Subhas; Ajila, Vidya; Castelino, Renita Lorina; Rao, Kumuda; Madi, Medhini
Journal of Dentistry Indonesia Vol. 25, No. 1
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Binder’s syndrome or maxillonasal dysostosis is a rare congenital condition that primarily affects the mid-face and sometimes the vertebrae. It was named after von Binder who described three cases of hypoplastic maxilla-nasal complex in 1962. It can either occur as a sporadic mutation or may be inherited in an autosomal recessive pattern with incomplete penetrance. Decrease in the naso-labial angle, flat forehead, dish-shaped face, absence of protrusion of nasal tip, absence of nasal flare with triangular or semilunar nostrils, palpable depression in the nasal floor and a class III tendency are characteristic of the syndrome. Vertebral anomalies are seen in some patients owing to the parallel development of the nasal complex and vertebrae in the third month of intrauterine life. Prenatal diagnosis may be done using ultrasonography at 21 weeks of pregnancy. A multi-disciplinary approach towards planning of treatment for individuals with Binder’s syndrome includes orthodontic treatment along with osteotomies and grafting to correct the nasal and mid-face defects.
Clinical and Radiographic Features of Nevoid Basal Cell Carcinoma Syndrome: A Case Report Babu, G Subhas; Pillai, Devika S; Hegde, Shruthi; Hegde, Padmaraj; Ajila, Vidya
Journal of Dentistry Indonesia Vol. 29, No. 3
Publisher : UI Scholars Hub

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Nevoid Basal Cell Carcinoma Syndrome, also called as Gorlin Gotz syndrome is an autosomal dominant disorder characterized by the presence of multiple odontogenic keratocysts (OKCs) of the jaw, basal cell carcinomas and skeletal anomalies. Presence of multiple OKCs is the first clinical manifestation in majority of the cases. Early diagnosis and treatment are of utmost importance in reducing the severity of this syndrome. We hereby report a rare case of Gorlin Goltz syndrome in a 28 years old female patient who presented with multiple cystic lesions in the jaws. Present case also highlights the clinical, radiographic and histopathologic features of this uncommon syndrome.
Co-Authors Babu, G Subhas Babu, Subhas Babu, Subhas G Castelino, Renita L Ghosh, Rumela Hegde, Padmaraj Hegde, Shruthi Kumuda Rao, Kumuda Madi, Medhini Madiyal, Ananya Nair, Mithula Pillai, Devika S Renita Lorina Castelino, Renita Lorina