Tumor necrosis factor receptor-associated periodic syndrome: A novel syndrome with cutaneous manifestations

Archives of Dermatology

Volumn 136, Issue 12, 2000, Pages 1487-1494

  Toro, J R ^a   Aksentijevich, I ^a   Hull, K ^a   Dean, J ^a   Kastner, D L ^a  

^a NATIONAL CANCER INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

TUMOR NECROSIS FACTOR RECEPTOR;

ADOLESCENT; ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; CONJUNCTIVITIS; DIAGNOSTIC PROCEDURE; EDEMA; ERYTHEMA; FEMALE; FEVER; GENE MUTATION; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; IMMUNOPHENOTYPING; INFLAMMATION; INFLAMMATORY DISEASE; LYMPHOCYTE; MALE; MICROSCOPY; MONOCYTE; PRIORITY JOURNAL; SKIN INFILTRATE; SKIN MANIFESTATION; SYNDROME; TRAP SYNDROME;

ADOLESCENT; ADULT; ANTIGENS, CD; CHILD; CHILD, PRESCHOOL; DIAGNOSIS, DIFFERENTIAL; FAMILIAL MEDITERRANEAN FEVER; FEMALE; HUMANS; IMMUNOPHENOTYPING; MALE; MIDDLE AGED; RECEPTORS, TUMOR NECROSIS FACTOR; RECEPTORS, TUMOR NECROSIS FACTOR, TYPE I; SKIN DISEASES; SYNDROME;

EID: 0034535910     PISSN: 0003987X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (74)

1. Germline mutations in the extracellular domains of the 55 kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammatory syndromes
2. Familial Hibernian fever
3. Clinical spectrum of familial Hibernian fever: A 14-year follow-up study of the index case and extended family
4. Gene localization for an autosomal dominant familial periodic fever to 12q13
5. Autosomal dominant familial Mediterranean fever-like syndrome with amyloidosis
6. Familial Mediterranean fever
7. Familial Mediterranean fever at the millennium: Clinical spectrum, ancient mutations, and a survey of 100 American referrals to the National Institutes of Health
8. Hyperimmunoglobulinemia D and periodic fever: A new syndrome
9. Hyperimmunoglobulinemia D and periodic fever syndrome: The clinical spectrum in a series of 50 patients
10. Autosomal dominant 'Mediterranean fever' in a Finnish family
11. A Dutch family with familial Mediterranean fever
12. Clinical syndromes resembling familial Mediterranean fever
13. A 38-year-old man with nephrotic syndrome, episodic fever and abdominal pain
14. A receptor for tumor necrosis factor defines an unusual family of cellular and viral proteins
15. The tumor necrosis factor ligand and receptor families
16. Antibodies to a soluble form of a tumor necrosis factor (TNF) receptor have TNF-like activity
17. A tumor necrosis factor-binding protein purified to homogeneity from human urine protects cells from tumor necrosis factor toxicity
18. The pathophysiology of tumor necrosis factors
19. TNF receptor-associated periodic fever syndrome (TRAPS): Novel TNFR1 mutations and early experience with etanercept therapy
20. T-cell subset analysis of peripheral T-cell lymphomas by paraffin section immunohistology and correlation of CD4/CD8 results with flow cytometry
21. Structure of the human TNF receptor 1 (p60) gene (TNFR1) and localization to chromosome 12p13
22. Linkage of familial Hibernian fever to chromosome 12p13
23. Ancient missense mutations in a new member of the RoRet gene family are likely to cause familial Mediterranean fever
24. A candidate gene for familial Mediterranean fever
25. The hereditary periodic fever syndromes: Molecular analysis of a new family of inflammatory diseases
26. B30.2-like domain proteins: Update and new insights into a rapidly expanding family of proteins
27. Mutation and haplotype studies of familial Mediterranean fever reveal new ancestral relationships and evidence for a high carrier frequency with reduced penetrance in the Ashkenazi Jewish population
28. MEFV-gene analysis in Armenian patients with familial Mediterranean fever: Diagnostic value and unfavorable renal prognosis of the M694V homozygous genotype-genetic and therapeutic implications
29. Pyrin/marenostrin mutations in familial Mediterranean fever
30. Non-founder mutations in the MEFV gene establish this gene as the cause of familial Mediterranean fever (FMF)
31. Familial Mediterranean fever in the 'Chuetas' of Mallorca: A question of Jewish origin or genetic heterogeneity
32. Mutations in the MEFV gene in a large series of patients with a clinical diagnosis of familial Mediterranean fever
33. Genes associated with periodic fevers highlighted at Dutch workshop
34. Mutations in the gene encoding mevalonate kinase cause hyper-IgD and periodic fever syndrome
35. Mutations in MVK, encoding mevalonate kinase, cause hyperimmunoglobulinaemia D and periodic fever syndrome
36. Regulation of the mevalonate pathway
37. The SREBP pathway: Regulation of cholesterol metabolism by proteolysis of a membrane-bound transcription factor
38. Hyperimmunoglobulinaemia D and periodic fever mimicking familial Mediterranean fever in the Mediterranean
39. Children with hyperimmunoglobulinemia D and periodic fever syndrome
40. Immunological studies in the hyper-immunogiobulin D syndrome
41. Arthritis in hyperimmunoglobulinaemia D
42. Occurrence of arthritis in hyperimmunoglobulinaemia D
43. Phenotype-genotype correlation in familial Mediterranean fever: Evidence for an association between Met694Val and amyloidosis
44. MEFV mutation analysis in patients suffering from amyloidosis of familial Mediterranean fever
45. Immunoglobulin D enhances the release of tumor necrosis factor-alpha and interleukin-1 beta as well as interleukin-1 receptor antagonist from human mononuclear cells
46. You give me fever
47. Cutaneous manifestations and histologic findings in the hyperimmunoglobulinemia D syndrome
48. IgD immune complex vasculitis in a patient with hyperimmunoglobulinemia D and periodic fever
49. Syndrome hyper-IgD: Manifestations cutanees
50. Syndrome hyper-IgD ou pseudo-maladie periodique: Manifestations cutanees dans 3 observations
51. Association of hyperimmunoglobulinemia D syndrome with erythema elevatum diutinum
52. Cutaneous manifestations of familial Mediterranean fever
53. Familial Mediterranean fever (recurrent hereditary polyserositis) in Arabs: A study of 175 patients and review of the literature
54. Familial Mediterranean fever: A survey of 470 cases and review of the literature
55. Familial Mediterranean fever in children
56. The cutaneous manifestations in children with familial Mediterranean fever (recurrent hereditary polyserositis): A six-year study
57. Familial Mediterranean fever in Arab children: The high prevalence and gene frequency
58. Erysipelas-like erythema of familial Mediterranean fever: Clinicopathologic correlation
59. Polyarteritis nodosa and familial Mediterranean fever
60. Polyarteritis nodosa and familial Mediterranean fever: A report of 2 cases and review of the literature
61. Perirenal and renal subcapsular haematoma as presenting symptoms of polyarteritis nodosa
62. Familial Mediterranean fever and polyarteritis nodosa: Experience of five paediatric cases: A causal relationship or coincidence?
63. Vasculitis in familial Mediterranean fever
64. Effect of prophylactic colchicine therapy on leukocyte function in patients with familial Mediterranean fever
65. Leukocyte chemotaxis in recurrent polyserositis (familial Mediterranean fever)
66. Colchicine alters the quantitative and qualitative display of selectins on endothelial cells and neutrophis
67. Colchicine in the prevention and treatment of the amyloidosis of familial Mediterranean fever
68. TNF receptor-associated periodic syndromes (TRAPS): Novel TNFR1 mutations and early experience with etanercept therapy
69. Tumor necrosis factor blockers in rheumatoid arthritis
70. Treatment options for rheumatoid arthritis: Celecoxib, leflunomide, etanercept, and infliximab
71. Neonatal onset multisystem inflammatory disease
72. Infantile-onset arthritis and multisystem inflammatory disease: 'A new syndrome'
73. Infantile-onset multisystem inflammatory disease: Radiologic findings
74. Periodic fever, aphthous stomatitis, pharyngitis, and adenopathy syndrome: Clinical characteristics and outcome