Nonsyndromic oligodontia in siblings: A rare case report

Nonsyndromic Oligodontia: a Rare Case Report with Review of Literature

Nonsyndromic Oligodontia with Ankyloglossia: a Rare Case Report

Agenesis of teeth is one of the most common human developmental anomalies. Oligodontia is a condition in which there is absence of six or more teeth, which itself is a rare condition. Oligodontia is associated with many syndromes. There is no much literature on oligodontia with ankylogossia. This is case report of a 9 year old girl child, who had missing permanent mandibular anterior teeth and ...

Nonsyndromic Familial Oligodontia with Multiple Dens Invaginatus: A Case Report of an Unusual Case

Oligodontia is a rare dental anomaly with a prevalence of 0.3% in permanent teeth and much less frequency in the primary dentition. Familial oligodontia represents an absence of varying numbers of primary and/or secondary teeth as an isolated trait. It is a complex and multifactorial condition. Many explanations-evolutionary, genetic, and environmental-have been proposed as the etiology. Simult...

Hypophosphatemic Rickets in Siblings: A Rare Case Report

Hypophosphatemic rickets (HR) is a type of hereditary rickets characterized by persistent hypophosphatemia and hyperphosphaturia. The most predominant type is inherited in an X-linked fashion and caused by mutation in the gene encoding the phosphate-regulating endopeptidase homolog, X-linked (PHEX), identified in 1995. The X-linked hypophosphatemic (XLH) rickets is a rare hereditary metabolic d...

Ellis–Van Creveld syndrome in siblings: A rare case report

Ellis-Van Creveld syndrome or chondroectodermal dysplasia is a rare autosomal recessive disorder presenting several skeletal manifestations and congenital heart malformations. Ellis-Van Creveld syndrome comprises of a tetrad of clinical manifestations of chondrodysplasia, polydactyly, ectodermal dysplasia, and cardiac defects. Here, we are presenting a very rare case of Ellis-Van Creveld syndro...