Turner Syndrome is a disorder of the X chromosome affecting girls with a prevalence of approximately 1/2500 to 1 in 3000 live female births. About 50 % of girls with Turner syndrome have monosomy X (45XO, pure form of TS). About 30% of girls with this disorder have Turner mosaic...
Open access
Research Article10.9734/ijrrd/2024/v7i2199
Background: Oral submucous fibrosis (OSMF) is regarded as a potentially malignant condition. It is characterized by a mucosal rigidity of variable intensity because of the fibroelastic changes of the juxta epithelial layer, resulting in a progressive inability to open the mouth....
Open access
Research Article10.9734/BJMMR/2016/23615
Leukoplakia is a potentially malignant disorder affecting the oral cavity. Early detection and prompt treatment are the keys to prevent its malignant transformation. Various treatment modalities have been discussed in multiple literatures, broadly categorized into non-surgical an...
Open access
Research Article10.9734/jcti/2025/v15i3304
Background: Von Recklinghausen’s disease also termed as “Neurofibromatosis type 1 (NF1)” is an autosomal dominant inherited disorder, characterized by various abnormalities such as neurofibroma, mainly in the skin and nerves. The classic manifestations include neurofibroma, café-...
Open access
Research Article10.9734/ijrrd/2025/v8i1204
Vascular anomalies or lesions consist of wide spectrum of congenital lesions of vascular origin. Broadly, it is classified into proliferative vascular tumors and nonproliferative vascular malformations. Based on the hemodynamic flow, vascular malformations can be classified as hi...
Open access
Research Article10.9734/ijrrd/2025/v8i1202