Συνώνυμα & Αναγραμματισμοί | Αγγλικά λέξη ATRESIA


ATRESIA

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Αριθμός γραμμάτων

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Είναι το παλτοδρόμιο

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Παραδείγματα χρήσης ATRESIA σε μια πρόταση

  • Esophageal atresia is a congenital medical condition (birth defect) that affects the alimentary tract.
  • He helped establish the biliary atresia program at CHOP when Japanese surgeon Morio Kasai came to work with him in the 1970s.
  • Morio Kasai (葛西 森夫, 1922–2008), a surgeon who developed the Kasai procedure for biliary atresia.
  • Sheena was born with an esophageal atresia in which the esophagus narrows as it approaches the stomach.
  • Biliary atresia, also known as extrahepatic ductopenia and progressive obliterative cholangiopathy, is a childhood disease of the liver in which one or more bile ducts are abnormally narrow, blocked, or absent.
  • Cardiac conditions in which there is decreased blood flow to the lungs such as, tetralogy of Fallot or pulmonary valve atresia, result in less blood becoming oxygenated.
  • Choanal atresia is a congenital disorder where the back of the nasal passage (choana) is blocked, usually by abnormal bony or soft tissue (membranous) due to failed hole development of the nasal fossae during prenatal development.
  • Ear canal stenosis & atresia can exist independently or may result from congenital malformations of the auricle such as microtia or anotia.
  • Cryptomenorrhea or cryptomenorrhoea, is a medical condition in which menstrual bleeding occurs but remains hidden due to a congenital septum or atresia blocking the vagina, resulting in symptoms of menstruation without external bleeding.
  • A liver biopsy may indicate too few bile ducts (bile duct paucity) or, in some cases, the complete absence of bile ducts (biliary atresia).
  • Lavage is also the initial treatment for duodenal atresia in newborns, a condition where the small intestine is closed distal to the stomach, causing food and fluid to accumulate in the stomach.
  • The classic clinical triad of Biliary atresia is acholic stools, and dark urine, jaundice, and hepatomegaly.
  • At puberty, clutches of follicles begin folliculogenesis, entering a growth pattern that ends in ovulation (the process where the oocyte leaves the follicle) or in atresia (death of the follicle's granulosa cells).
  • Other variants include cloacal malformation, rectal atresia, rectal stenosis, and anterior ectopic anus.
  • Pulmonary atresia with ventricular septal defect (PA-VSD) is identified by underdevelopment of the right ventricle.
  • If the neonatal jaundice is not resolved with simple phototherapy, other causes such as biliary atresia, Progressive familial intrahepatic cholestasis, bile duct paucity, Alagille syndrome, alpha 1-antitrypsin deficiency, and other pediatric liver diseases should be considered.
  • First described in 1979, the acronym "CHARGE" came into use for newborn children with the congenital features of coloboma of the eye, heart defects, atresia of the nasal choanae, restricted growth or development, genital or urinary abnormalities, and ear abnormalities and deafness.
  • Conditions addressed by labiaplasty include congenital defects and abnormalities such as vaginal atresia (absent vaginal passage), Müllerian agenesis (malformed uterus and fallopian tubes), intersex conditions (male and female sexual characteristics in a person); and tearing and stretching of the labia minora caused by childbirth, accident, and age.
  • Esophagectomy is also occasionally performed for benign disease such as esophageal atresia in children, achalasia, or caustic injury.
  • Other abdominopelvic or perineal congenital anomalies frequently prompt radiographic evaluation in the newborn, resulting in a diagnosis of coincident vaginal atresia.



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