Osteolytic Lesion in PAPA Syndrome Responding to Anti-interleukin 1 Treatment

[1] An Autoinflammatory Disease with Deficiency of the Interleukin-1-Receptor Antagonist [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2009, 360 (23) : 2426 - 2437

[2] Genotype, phenotype, and clinical course in five patients with PAPA syndrome (pyogenic sterile arthritis, pyoderma gangrenosum, and acne) [J]. ARTHRITIS AND RHEUMATISM, 2012, 64 (06): : 2022 - 2027

[3] Homozygous mutations in LPIN2 are responsible for the syndrome of chronic recurrent multifocal osteomyelitis and congenital dyserythropoietic anaemia (Majeed syndrome) [J]. JOURNAL OF MEDICAL GENETICS, 2005, 42 (07) : 551 - 557

[4] A missense mutation in pstpip2 is associated with the murine autoinflammatory disorder chronic multifocal osteomyelitis [J]. BONE, 2006, 38 (01) : 41 - 47

[5] Current Understanding of the Pathogenesis and Management of Chronic Recurrent Multifocal Osteomyelitis [J]. CURRENT RHEUMATOLOGY REPORTS, 2012, 14 (02) : 130 - 141

[6] Efficacy of anti-IL-1 treatment in Majeed syndrome [J]. ANNALS OF THE RHEUMATIC DISEASES, 2013, 72 (03) : 410 - 413

[7] The SAPHO Syndrome [J]. SEMINARS IN ARTHRITIS AND RHEUMATISM, 2012, 42 (03) : 254 - 265

[8] Pyrin binds the PSTPIP1/CD2BP1 protein, defining familial Mediterranean fever and PAPA syndrome as disorders in the same pathway [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (23) : 13501 - 13506

[9] Smith EJ, 2010, CURR GENOMICS, V11, P519, DOI 10.2174/138920210793175921

[10] Mutations in CD2BP1 disrupt binding to PTP PEST and are responsible for PAPA syndrome, an autoinflammatory disorder [J]. HUMAN MOLECULAR GENETICS, 2002, 11 (08) : 961 - 969

[1] An Autoinflammatory Disease with Deficiency of the Interleukin-1-Receptor Antagonist [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2009, 360 (23) : 2426 - 2437

[2] Genotype, phenotype, and clinical course in five patients with PAPA syndrome (pyogenic sterile arthritis, pyoderma gangrenosum, and acne) [J]. ARTHRITIS AND RHEUMATISM, 2012, 64 (06): : 2022 - 2027

[3] Homozygous mutations in LPIN2 are responsible for the syndrome of chronic recurrent multifocal osteomyelitis and congenital dyserythropoietic anaemia (Majeed syndrome) [J]. JOURNAL OF MEDICAL GENETICS, 2005, 42 (07) : 551 - 557

[4] A missense mutation in pstpip2 is associated with the murine autoinflammatory disorder chronic multifocal osteomyelitis [J]. BONE, 2006, 38 (01) : 41 - 47

[5] Current Understanding of the Pathogenesis and Management of Chronic Recurrent Multifocal Osteomyelitis [J]. CURRENT RHEUMATOLOGY REPORTS, 2012, 14 (02) : 130 - 141

[6] Efficacy of anti-IL-1 treatment in Majeed syndrome [J]. ANNALS OF THE RHEUMATIC DISEASES, 2013, 72 (03) : 410 - 413

[7] The SAPHO Syndrome [J]. SEMINARS IN ARTHRITIS AND RHEUMATISM, 2012, 42 (03) : 254 - 265

[8] Pyrin binds the PSTPIP1/CD2BP1 protein, defining familial Mediterranean fever and PAPA syndrome as disorders in the same pathway [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (23) : 13501 - 13506

[9] Smith EJ, 2010, CURR GENOMICS, V11, P519, DOI 10.2174/138920210793175921

[10] Mutations in CD2BP1 disrupt binding to PTP PEST and are responsible for PAPA syndrome, an autoinflammatory disorder [J]. HUMAN MOLECULAR GENETICS, 2002, 11 (08) : 961 - 969