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692 Possible Causes for Leukocyte Adhesion Deficiency

  • Leukocyte Adhesion Deficiency Syndrome

    Leukocyte-adhesion deficiency syndromes are rare, autosomal recessive, hereditary immunological disorders.[ncbi.nlm.nih.gov] deficiency edit English leukocyte-adhesion deficiency syndrome Human disease leukocyte adhesion deficiency Congenital leukocyte adherence deficiency (disorder) Congenital[wikidata.org] We have previously reported a newly discovered congenital disorder of neutrophil adhesion, leukocyte adhesion deficiency syndrome type 2 (LAD II).[ncbi.nlm.nih.gov]

  • Omphalitis

    [Leukocyte adhesion deficiency syndrome: case report] [Spanish]. Rev Alerg Mex. 1999 Sep-Oct. 46 (5):140-4. [Medline]. van Vliet DN, Brandsma AE, Hartwig NG.[emedicine.com] Commonly Associated Conditions Leukocyte adhesion deficiency Omphalitis may be the initial manifestation of one of the leukocyte adhesion deficiencies (LADs).[unboundmedicine.com] Leukocyte adhesion deficiency disorder: report of one case. Acta Paediatr Taiwan. 1999 Mar-Apr. 40(2):128-31. [Medline].[emedicine.com]

  • Hereditary Neutrophilia

    […] porphyria, Leukemoid reaction, Leukocyte adhesion deficiency type 1, Leukocyte adhesion deficiency type 2, Leukocyte adhesion deficiency type 3, Lymphangitis, Polycythaemia[wikidoc.org] , hereditary Leukocyte adhesion deficiency - type 1 Leukocyte adhesion deficiency - type 2 Leukocyte adhesion deficiency type 1 Leukocyte adhesion deficiency type 2 Leukocyte[icd9data.com] - type 2 Leukocyte adhesion deficiency type 1 Leukocyte adhesion deficiency type 2 Leukocyte disorder, genetic May hegglin anomaly Pelger-huet anomaly Pelger-huët anomaly[icd10data.com]

  • Gingivitis

    Hyperplastic gingivitis is a rare manifestation of granulomatosis with polyangiitis (GPA). This gingivitis has a very distinctive clinical appearance (so-called Strawberry gingivitis) and when seen is virtually pathognomic for GPA. Gingivitis often precedes other organ involvement therefore making awareness of this[…][ncbi.nlm.nih.gov]

  • Neutrophil Immunodeficiency Syndrome

    Clinical description Neutrophil immunodeficiency syndrome presents as similar to leukocyte-adhesion deficiency (LAD; see this term), however there is no evidence of deficiency[orpha.net] Leukocyte adhesion deficiency type I (LAD1) is the result of mutations in a gene called CD18.[primaryimmune.org] Leukocyte adhesion deficiency type III (LAD3) is caused by mutations in a gene called FERMT3.[primaryimmune.org]

  • Complement Deficiency Syndrome

    ) CR3/CR4 1:1,000,000 Leukocyte adhesion deficiency CD59 1-2:1,000,000 Paroxysmal nocturnal hemoglobuinuria Complement System Deficiency Diseases References 1.[sinobiological.com] Other symptoms of complement deficiency diseases (like hereditary angioedema, paroxysmal nocturnal hemoglobinuria, or leukocyte adhesion deficiency syndrome) include abdominal[medical-dictionary.thefreedictionary.com] […] infection C7 70 (0.0041% Japan) Meningococcal infection C8 70 (0.0027% Japan) Meningococcal infection C9 1:1000 and 0.0027% Japan Meningococcal infection (less than C5-C8 deficiency[sinobiological.com]

  • Bleeding Disorder due to CalDAG-GEFI Deficiency

    Cell adhesion and leukocyte adhesions defects. In: Smith EM, Puck J, Ochs HD eds. Primary Immune deficiency disease. A molecular and genetic approach, 2nd ed.[link.springer.com] Loss Of Gene Involved In Clot Formation May Explain Bleeding Disorder, LAD-III 09 23 15' Patients with the syndrome leukocyte adhesion deficiency (LAD) III suffer from recurrent[bphmeds.net] […] antigen; HPS, Hermansky-Pudlak syndrome; Ig, immunoglobulin; LAD, leukocyte adhesion deficiency; MIDAS, metal ion-dependent adhesion site; PAR, protease-activated receptor[accessmedicine.mhmedical.com]

  • Skin Infection

    Leukocyte adhesion deficiency (LAD) I is a well-described genetic disorder in which leukocytes are unable to migrate to sites of inflammation due to mutations in the ITGB2[ncbi.nlm.nih.gov] The hyperadhesiveness rather than adhesion deficiency of the patient's leukocytes suggests that a novel lesion in a pathway regulating integrin adhesion is responsible for[ncbi.nlm.nih.gov]

  • Hypersensitivity

    Patients with leukocyte adhesion deficiency (loss of LFA-1, Mac-1 and p150,95 proteins) have recurrent bacterial and fungal infections since polymorphonuclear cells cannot[dermatology.cdlib.org] ICAM-1 binds LFA-1 on leukocytes.[dermatology.cdlib.org]

  • Periodontitis

    adhesion deficiency syndromes Papillon-Lefèvre syndrome Chédiak-Higashi syndrome Histiocytosis syndromes Infantile genetic agranulocytosis Hypophosphatasia Cohen syndrome[merckmanuals.com] adhesion deficiency syndromes, Papillon-Lefèvre syndrome, Chediak-Higashi syndrome, histiocytosis syndromes, glycogen storage disease, infantile genetic agranulocytosis,[cda-adc.ca] Periodontitis Associated with Systemic Disease: These associated diseases included Hypophosphatasia, Neutropenia, Papillon Lefevre Syndrome, Leukocyte Adhesion Deficiency,[drbui.com]

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