1. Introduction
Rigid temporization has been recognized to have a significant impact on the peri-implant tissue response in immediate implant
loading since it reduces the mechanical stress exerted on each.

1. Abstract
Schistosomiasis is a parasitic disease commonly found in en demic regions such as sub-Saharan Africa, the Middle East, and parts of Asia. However, cases in non-endemic countries like.

1. Abstract
A 32-year-old male presented with recurrent abdominal pain for two years. Esophagogastroduodenoscopy revealed duodenal wall penetration by a metallic foreign body, subsequently identified via computed tomography as an inferior vena cava.

Abstract .1
A 34-year-old young female patient was admitted to hospital with abdominal discomfort and intermittent fever for more than 1 month. Puncture pathological result: except 1.

1. Abstract
Boerhaave syndrome is a rare, life-threatening condition. Symptoms are often atypical, so early diagnosis is crucial for prompt treatment.

1. Abstract
1.1. Background
Salmonella is a genus of bacteria that is primarily recognized for causing foodborne illnesses and gastrointestinal infections. However, cases involving empyema attributed to Salmonella remain quite rare, with only a handful of cases reported in the medical literature.

1. Abstract
1.1. Introduction
Myomatous-erythrocytic syndrome is an exceptionally rare clinical entity characterized by the coexistence of giant uterine leiomyomas defined as fibroids measuring ≥20 cm and erythrocytosis, marked by an abnormal elevation in red blood cell mass, hemoglobin, and hematocrit.

1. Abstract
Stop NOx elimination by ammonia. Stop water clean centre. Abandon bonfire inhibition rule. These 3 items are essential to promote CO2 assimilation to stop global warming stop.

1. Abstract
Familial partial lipodystrophy (FPLD) is a heterogeneous group of rare genetic disorders (estimated prevalence <1/100,000) characterized by a lipodystrophy phenotype combined with metabolic abnormalities such as insulin resistance and hypertriglyceridemia. Several subtypes have been described

1. Abstract
Hypertrophic obstructive cardiomyopathy (HOCM) is a genetically driven cardiac condition most often involving asymmetric septal hypertrophy. Mid-ventricular and apical variants are rare, accounting for less than 5% of cases in Western populations, and present unique diagnostic and prognostic challenges.