HEREDITARY MICROSPHEROCYTIC HEMOLYTIC ANEMIA (MINKOWSKI-CHAUFFARD DISEASE)

Authors

  • Ruziev Zarif Muhammadovich Department of Hematology and Clinical Laboratory Diagnostics Bukhara State Medical Institute Bukhara, Uzbekistan

Keywords:

hereditary microspherocytosis, hemolytic anemia, clinical case

Abstract

Hereditary microspherocytic hemolytic anemia was first described over a century ago by the German physician Oskar Minkowski and the French therapist Anatole Chauffard, who singled out the disease from the group of hemolytic syndromes as a special nosology. This disease has not lost its relevance even today, as it is still a widespread disease of the hereditary type with an incidence rate of 1:5000 live-born children of both sexes, including mild and subclinical forms - 1:2000 live-born children of both sexes. Minkowski - Chauffard hemolytic anemia is encountered quite often in the practical work of a pediatrician, therefore the main methods of diagnosing this disease, providing assistance to children in a state of hemolytic crisis, as well as recommendations during the remission period should be well known to a pediatrician in any area of practical work.

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Published

2024-09-04

How to Cite

Muhammadovich, R. Z. (2024). HEREDITARY MICROSPHEROCYTIC HEMOLYTIC ANEMIA (MINKOWSKI-CHAUFFARD DISEASE). EUROPEAN JOURNAL OF MODERN MEDICINE AND PRACTICE, 4(9), 105–107. Retrieved from https://inovatus.es/index.php/ejmmp/article/view/3960

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