Pustular Psoriasis
What's New
Last Posted: Jul 04, 2024
- Rare Filaggrin Variants Are Associated with Pustular Skin Diseases in Asians.
Luca Lo Piccolo, et al. International journal of molecular sciences 2024 0 (12) - Targeted review of IL36RN mutations in patients with generalised pustular psoriasis.
James G Krueger, et al. Skin health and disease 2024 0 (2) e343 - Expression of interleukin-36 receptor antagonist in a patient with generalized pustular psoriasis harboring the p.Pro82Leu variant in the IL36RN gene.
Itsumi Mizukawa, et al. The Journal of dermatology 2023 0 - Identification of the BTN3A3 gene as a molecule implicated in generalized pustular psoriasis in a Chinese population.
Zhang Qilin, et al. The Journal of investigative dermatology 2023 0 - Newly revealed variants of SERPINA3 in generalized pustular psoriasis attenuate inhibition of ACT on cathepsin G.
Liu Yaqin, et al. Journal of human genetics 2023 0 - [Genetic Polymorphism of IL36RN in Han Patients with Generalized Pustular Psoriasis Alone in Sichuan Region].
Li Zhong-Tao, et al. Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition 2018 0 (4) 582-586 - Clinical and genetic differences between pustular psoriasis subtypes.
Twelves Sophie, et al. The Journal of allergy and clinical immunology 2018 0 (3) 1021-1026 - Lack of association between mutation in IL36RN and palmoplantar pustular psoriasis in Chinese patients.
Xiaoling Yu, et al. Anais brasileiros de dermatologia 2019 0 (6) 658-663 - Myeloperoxidase Modulates Inflammation in Generalized Pustular Psoriasis and Additional Rare Pustular Skin Diseases.
Haskamp Stefan, et al. American journal of human genetics 2020 0 (3) 527-538 - Clinical background of patients with psoriasiform skin lesions due to tumor necrosis factor antagonist administration at a single center.
Mori Miho, et al. The Journal of dermatology 2021 0 (11) 1745-1753
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Rare Disease PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to rare diseases...more
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Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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