IDENTIFICATION AND VERIFICATION OF HEREDITARY SPHEROCYTOSIS BY MEANS OF LABORATORY DIAGNOSIS

• Główni autorzy: Yu. A. Prokhorova (Autor), E. E. Zueva (Autor), N. E. Sokolova (Autor), G. N. Salogub (Autor), V. I. Golubeva (Autor)
• Format: Książka
• Wydane: Union of pediatricians of Russia, 2014-07-01T00:00:00Z.
• Hasła przedmiotowe: article
• Dostęp online: Connect to this object online.

Aim. Hereditary spherocytosis (HS) is the most commonly encountered erythrocyte membranopathy. Frequency of occurrence of the disease makes one case per 2000−5000 newborns. Hereditary spherocytosis often causes a complex of clinical signs, including hemolytic crises in patients. At the same time man...