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 th...
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| Huvudupphov: | , , , , |
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| Materialtyp: | Artigo |
| Språk: | Russo |
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The Publishing House Medicine and Enlightenment
2022-08-01
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| Serie: | Мать и дитя в Кузбассе |
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| Länkar: | https://mednauki.ru/index.php/MD/article/view/751 |
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