introduction congenital microgastria is an extremely rare anomaly, which is due to failure of gastric development, and causes a tubular stomach with reduced capacity. it is almost always associated with other congenital anomalies. case presentation the patient was a two-month-old boy with microgastria in association with gastroesophageal reflux, tracheomalacia, and limb defect. discussion most ...

this case of a female patient, 14 yr old with association of the two anomalies, which we came across with in 2014, is rarely met in the specialty practice. the impacted canines are part of the group of dental anomalies of position, while the agenesis is part of the group of dental number anomalies. the orthodontic treatment in the two arches has to be differentiated, the therapeutic objectives ...

SUMMARY Holt Oram Syndrome consisting of upper limb defcts, cardiac anomalies and narrow shoulder, was first described by Holt and Oram in 1960. The inheritance pattern is autosomal dominant and most commonly encoutered cardiac anomalies being ASD, although all variaties of C.H.D are reported. Upper limb anomalies are not specific, although scaphoid bone deformity is almost characteristic in t...

To assess the quality and appropriateness of Canadian Congenital Anomalies Surveillance System (CCASS), a system based on routine hospital admission/separation records, we compared the congenital anomalies ascertained by CCASS for the period of January 1, 1990 to December 31, 1993 in the province of Alberta with corresponding figures obtained from Alberta Congenital Anomalies Surveillance Syste...

Congenital renal fusion anomalies, characterized by either partial or complete fusion of the two kidneys, are represented by horseshoe kidney, crossed renal ectopia with fusion and fused pelvic cake kidney. Though these anomalies may remain asymptomatic, in certain cases they may be associated with pathological conditions like nephrolithiasis, hydronephrosis, recurrent urinary tract infections,...