CONGENITAL corneal opacities vary greatly in extent and location and are usually associated with other anomalies of the anterior segment. Although a variety of clinical terms, such as cornea plana, sclerocornea, Rieger's anomaly, Axenfeld's syndrome, has been used to describe these anomalies, recent evidence (Goldstein and Cogan, 1962) suggests that they are all closely related entities. Theodo...

Submit Manuscript | http://medcraveonline.com Abbreviations: CKD: Chronic Kidney Disease; AKI: Acute Kidney Injury; PE: Pre-Eclampsia; SLE: Systemic Lupus Erythematosus; RA: Rheumatoid Arthritis; SS: Systemic Scleroderma; ESRD: End-Stage Renal Disease; CVDs: Cardiovascular Diseases; GFR: Glomerular Filtration Rate; sCR: Serum Creatinine; LLAC: Lupuslike anticoagulant; PE-AKI: Preeclampsia Acute...

Submit Manuscript | http://medcraveonline.com Abbreviations: CKD: Chronic Kidney Disease; AKI: Acute Kidney Injury; PE: Pre-Eclampsia; SLE: Systemic Lupus Erythematosus; RA: Rheumatoid Arthritis; SS: Systemic Scleroderma; ESRD: End-Stage Renal Disease; CVDs: Cardiovascular Diseases; GFR: Glomerular Filtration Rate; sCR: Serum Creatinine; LLAC: Lupuslike anticoagulant; PE-AKI: Preeclampsia Acute...

OBJECTIVE The extracardiac conduit procedure is widely used for patients with heterotaxy syndrome with complex systemic and pulmonary venous anomalies; however, it lacks conduit-growth potential and requires long-term anticoagulation. We present the intracardiac Fontan procedure, which eliminates the above-mentioned disadvantages. PATIENTS AND METHODS Twenty-four patients (mean age, 4.1 years...

Background  H syndrome is an autosomal recessive genodermatosis with a low prevalence which is caused by a mutation in SLC29A3 gene. This disorder is characterized by sclerotic, hyperpigmented, hypertrichotic cutaneous plaques with systemic involvement including: hepatosplenomegaly, heart anomalies, hearing loss, hypogonadism, low height, and hyperglycemia. Case Presentation  Here we have pres...

Background: Complete colonic duplication is a very rare congenital anomaly that may have different presentations according to its location and size. Complete colonic duplication can occur in 15% of gastrointestinal duplication. We report two cases of complete colonic duplications, and their characteristics. Case Presentation: We present two patients with complete colonic duplication with differ...

The research objectives were to determine the prevalence of impacted teeth in orthodontic patients Israel, examining epidemiological and genetic linkage. Methods: Data was collected from cohort treated Tel-Aviv University between 2010–2017. Forty-five for randomly selected, compared 45 control patients, paired by age sex. Collected data included: week birth, type medical history, dental anomali...

background: complete colonic duplication is a very rare congenital anomaly that may have different presentations according to its location and size. complete colonic duplication can occur in 15% of gastrointestinal duplication. we report two cases of complete colonic duplications, and their characteristics. case presentation: we present two patients with complete colonic duplication with differ...