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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Main Authors: | , , , , , , , |
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Format: | Book |
Published: |
"Paediatrician" Publishers LLC,
2014-12-01T00:00:00Z.
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Online Access: | Connect to this object online. |
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Internet
Connect to this object online.3rd Floor Main Library
Call Number: |
A1234.567 |
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Copy 1 | Available |