Super Points

SUPERStudy: Folate Supplementation in Pregnancy

SUPERStudy: Folate Supplementation in Pregnancy Introduction: Folate (vitamin B9) is an essential nutrient during pregnancy, playing a crucial role in DNA synthesis, cell division, and the formation of the neural tube in the developing fetus. Folate supplementation is critical for preventing neural tube defects (NTDs) such as spina bifida and anencephaly. Pathophysiology: During pregnancy, folate […]

SUPERStudy: Organophosphate Poisoning

Introduction Organophosphate poisoning is a potentially life-threatening condition caused by exposure to organophosphate (OP) compounds. These agents irreversibly inhibit acetylcholinesterase, leading to the accumulation of acetylcholine and overstimulation of cholinergic receptors. Etiology Sources: Agricultural pesticides (e.g., malathion, parathion). Chemical warfare agents (e.g., sarin, VX gas). Ophthalmologic agents for glaucoma (e.g., echothiophate, isoflurophate). Accidental exposure or […]

SUPERStudy: HPV Vaccine 

Introduction: Human papillomavirus (HPV) is the most common sexually acquired infection in the world. The human papillomavirus (HPV) vaccine is a preventive measure aimed at reducing the incidence of HPV-related diseases, including cervical, anal, oropharyngeal, and other cancers, as well as genital warts. HPV is a common sexually transmitted infection, and certain high-risk types (e.g., […]

Meconium Ileus

Introduction Meconium ileus is a neonatal intestinal obstruction caused by abnormally thick and sticky meconium, typically located in the distal ileum. It is a hallmark of cystic fibrosis (CF) and often the first presentation of this genetic disorder. Etiology Primary Cause: Cystic fibrosis due to mutations in the CFTR gene, leading to abnormal chloride and […]

SUPERStudy: Choriocarcinoma

  Introduction: Choriocarcinoma is a highly malignant type of gestational trophoblastic disease (GTD) that arises from abnormal trophoblastic tissue following pregnancy. It is characterized by the proliferation of syncytiotrophoblasts and cytotrophoblasts without the formation of villi. This tumor is highly vascular and prone to hematogenous spread, making it an aggressive cancer. Epidemiology: Choriocarcinoma is reported […]

Congenital Aganglionic Megacolon (Hirschsprung Disease)

Introduction Congenital aganglionic megacolon, or Hirschsprung disease (HD), is a congenital disorder characterized by the absence of ganglion cells in the distal bowel due to neural crest cell migration failure during fetal development. This results in a lack of coordinated peristalsis and functional obstruction. Pathophysiology Neural Crest Cell Migration Failure: Ganglion cells in the submucosal […]

SUPERStudy: Ventricular Septal Defect 

Introduction: Ventricular septal defect (VSD) is a hole in the wall that separates the right and left ventricles of the heart, resulting in shunt formation.  – They are the most prevalent congenital cardiac anomaly in children and the second most common in adults, surpassed only by bicuspid aortic valves.  Etiology: can occur with other congenital […]

SUPERStudy: Patent Ductus Arteriosus (PDA) 

  Introduction: Patent ductus arteriosus (PDA) is a persistence of the in utero communication between the aortic and pulmonary arteries after birth causing a left-to-right shunt. Risk factors: Maternal rubella infection; prematurity; high altitude, genetic problems such as Down syndrome  Pathophysiology:  In the fetal circulation, superior vena cava blood enters the right atrium and characteristically […]

SUPERStudy: VACTERL Association 

Introduction VACTERL association is a nonrandom constellation of congenital anomalies involving multiple organ systems. The acronym stands for: V: Vertebral anomalies A: Anal atresia C: Cardiac defects T: Tracheoesophageal fistula E: Esophageal atresia R: Renal anomalies L: Limb defects Patients often present with at least three of these anomalies, without a unifying genetic or environmental […]

SUPERStudy: Familial hypercholesterolemia (FH) 

from www.supertestscores.com   Introduction: Familial hypercholesterolemia (FH) is a group of autosomal dominant and recessive disorders of lipoprotein metabolism characterized by strikingly elevated low-density lipoprotein-cholesterol (LDL-C), the presence of xanthomas, and premature atherosclerosis.  Epidemiology: Homozygous 1 in 1 million; Heterozygous 1 in 500   Pathogenesis: Pathogenic variations in the following four genes can cause FH: (1) […]