FARBER DISEASE - DISEASE DESCRIPTION WITH CASE REPORTS

Farber disease (lipogranulomatosis, OMIM 228000) - is extremely rare autosomal-recessive disorder from group of lysosomal storage disorders, due to deficiency of acid ceramidase activity enzyme. Farber disease has a lot of clinical masques and resembles to different inflammatory disorders, such as j...

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Detalhes bibliográficos
Main Authors: I. A. Chikova (Author), N. V. Buchinskaya (Author), М. М. Kostik (Author), V. V. Avramenko (Author), O. L. Krasnogorskaya (Author), R. A. Nasirov (Author), T. Levade (Author), V. G. Chasnyk (Author)
Formato: Livro
Publicado em: "Paediatrician" Publishers LLC, 2014-12-01T00:00:00Z.
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