A RARE DISEASE OF CONGENITAL HISTIOCYTOSIS FROM LANGERHANS CELLS IN A NEW-BORN BABY
Histiocytosis from Langerhans cells (НCL) is a rare disease. HCL is not a hereditary, genetically determined disease. The epidemiology of HCL has not been studied enough. Purpose of the study - the aim is to present a clinical case of Langerhans cell histiocytosis (HCL) in a newborn and describe the...
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| Main Authors: | , , , , |
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| Format: | Book |
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The Publishing House Medicine and Enlightenment,
2022-08-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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