Macrodontia is a rare but cosmetically challenging dental anomaly. The following case report is described of a young girl with macrodontia central incisors who was treated with direct composite veneer and gingival color composite. The aesthetic outcome was satisfactory without unnecessary loss of teeth.  

Introduction Nutcracker syndrome is a rare disease entity that is caused by entrapment of the left renal vein between the aorta and superior mesenteric artery, usually due to abnormal branching of the superior mesenteric artery from the aorta causing renal venous hypertension. The symptoms vary from asymptomatic hematuria to severe pelvic congestion. Celiacomes-enteric trunk anomaly is a rare v...

In 1976, Gonzales-Crussi et al. (Am. J. Dis. Child. 130:1015-18, 1976) introduced the first case of bridging bronchus as a rare bronchial branching anomaly; since then, only 14 worldwide cases was described. We suggest our case might be number 15 and could be the first case of type six of this bronchial anomaly. We present a case of a 10-month-old infant with bridging bronchus, congenital trach...

Retrocaval ureter is a relatively rare developmental anomaly of the inferior vena cava. It commonly manifests in the third to fourth decade of life; however, pediatric reports of this condition are very rare. Individuals with this anomaly are symptomatic because of ureteric obstruction. All symptomatic patients need surgery where the ureter is divided and anastomosed anterior to inferior vena c...

Double right coronary artery is a relatively rare coronary anomaly. In this case report we aim to increase awareness of the importance of recognizing such anomaly and a brief literature review of similar cases and possible high risk features. Computed Tomography is well recognized modality to detect coronary anomaly and in our case we demonstrated this as well.

Aplasia of the nose is a very rare, congenital anomaly in our field. It emerges as a complete absence of the external nose and all nasal cavities on both sides, or an absence of one half of the nose and its associated nasal cavity. The latter case is called "halfnose." Etiologically, it is akin to tubular proboscis, anomaly with a snout-like nasal appendage on, or by the mid-line of the face. T...

Lateral sacral lipomyelomeningocele is a rare spinal developmental anomaly. In the case under report, the fat attached to the neural placode was blending with the gluteal fat externally. The cord was tethered at this level. Multiple bony anomalies and diastematomyelia were associated findings. A case of lateral sacral lipomyelomeningocele with excellent imaging detail provided by the multiplana...

Submit Manuscript | http://medcraveonline.com 100 cases have been reported in the literature. It was classified into four types by Smith in his review of 11 cases in 1946 [2]. Bilateral ureteral triplication is rare than bilateral ureteral duplication. Only 5 cases of bilateral ureteral triplication have been reported so far in medical literature [3]. Furthermore, ureteral triplication is occas...

Unexpected and puzzling variations in bronchial anatomy might be discovered during bronchoscopy. The occurrence of congenital tracheobronchial anomaly is estimated to range between 1% and 12% of the overall population.1 We present 2 rare cases of congenital bronchial anomaly that were discovered during bronchoscopy and that emphasize the value of computed tomogram (CT) in diagnosing congenital ...