Condition
Leukocyte-Adhesion Deficiency Syndrome
General Healthcare
Overview
Rare, autosomal recessive disorder caused by deficiency of the beta 2 integrin receptors (RECEPTORS, LEUKOCYTE-ADHESION) comprising the CD11/CD18 family of glycoproteins. The syndrome is characterized by abnormal adhesion-dependent functions, especially defective tissue emigration of neutrophils, leading to recurrent infection.
This information is general and should not be treated as medical advice. Always speak directly with a qualified healthcare professional before making decisions about treatment, diagnosis, procedures, medicines or care.
Quick facts about Leukocyte-Adhesion Deficiency Syndrome
- Topic type
- Condition
- Category
- General Healthcare
- MeSH classification
- C16.320.798.719|C20.673.795.719
Preparing for an appointment about Leukocyte-Adhesion Deficiency Syndrome
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Source: Medical Subject Headings (MeSH), produced by the U.S. National Library of Medicine. EuroCareFinder is not endorsed by the National Library of Medicine. MeSH version: 2026.