[1] |
张抒扬, 张学. 近年中国罕见病相关政策和实践探索[J]. 罕见病研究, 2022, 1(1): 1-6. doi: 10.12376/j.issn.2097-0501.2022.01.001
|
[2] |
Feng S, Liu S, Zhu C, et al. National rare diseases registry system of China and related cohort studies: vision and roadmap[J]. Hum Gene Ther, 2018, 29(2): 128-135. doi: 10.1089/hum.2017.215
|
[3] |
张学军. 罕见性遗传性皮肤病的研究现状及展望[J]. 皮肤科学通报, 2020, 37(1): 1-4. https://www.cnki.com.cn/Article/CJFDTOTAL-ZYXW202001001.htm
|
[4] |
He PP, He CD, Cui Y, et al. Refined localization of dyschromatosis symmetrica hereditaria gene to a 9.4-cM region at 1q21-22 and a literature review of 136 cases reported in China[J]. Br J Dermatol, 2004, 150(4): 633-639. doi: 10.1111/j.0007-0963.2004.05861.x
|
[5] |
Xing QH, Wang MT, Chen XD, et al. A gene locus responsible for dyschromatosis symmetrica hereditaria (DSH) maps to chromosome 6q24.2-q25.2[J]. Am J Hum Genet, 2003, 73(2): 377-382. doi: 10.1086/377007
|
[6] |
Zhang Z, Niu Z, Yuan W, et al. Fine mapping and identification of a candidate gene SSH1 in disseminated superficial actinic porokeratosis[J]. Hum Mutat, 2004, 24(5): 438.
|
[7] |
Zhang ZH, Niu ZM, Yuan WT, et al. A mutation in SART3 gene in a Chinese pedigree with disseminated superficial actinic porokeratosis[J]. Br J Dermatol, 2005, 152(4): 658-663. doi: 10.1111/j.1365-2133.2005.06443.x
|
[8] |
Lin Z, Chen Q, Lee M, et al. Exome sequencing reveals mutations in TRPV3 as a cause of Olmsted syndrome[J]. Am J Hum Genet, 2012, 90(3): 558-564. doi: 10.1016/j.ajhg.2012.02.006
|
[9] |
Wu Y, Li G, Zhu X. A novel homozygous point mutation in the COL17A1 gene in a Chinese family with generalized atrophic benign epidermolysis bullosa[J]. J Dermatol Sci, 2002, 28(3): 181-186. doi: 10.1016/S0923-1811(01)00163-3
|
[10] |
Feng YG, Xiao SX, Ren XR, et al. Keratin 17 mutation in pachyonychia congenita type 2 with early onset sebaceous cysts[J]. Br J Dermatol, 2003, 148(3): 452-455. doi: 10.1046/j.1365-2133.2003.05152.x
|
[11] |
He PP, Zhang XJ, Yang Q, et al. Refinement of a locus for Marie Unna hereditary hypotrichosis to a 1.1-cM interval at 8p21.3[J]. Br J Dermatol, 2004, 150(5): 837-842. doi: 10.1111/j.1365-2133.2004.05913.x
|
[12] |
Yang Y, Wang Y, Li S, et al. Mutations in SCN9A, encoding a sodium channel alpha subunit, in patients with primary erythermalgia[J]. J Med Genet, 2004, 41(3): 171-174. doi: 10.1136/jmg.2003.012153
|
[13] |
Wang B, Yang W, Wen W, et al. Gamma-secretase gene mutations in familial acne inversa[J]. Science, 2010, 330(6007): 1065. doi: 10.1126/science.1196284
|
[14] |
Wei A, Zhang T, Yuan Y, et al. Spectrum analysis of albinism genes in a large cohort of Chinese index patients[J]. J Invest Dermatol, 2022, 142(6): 1752-1755. e3. doi: 10.1016/j.jid.2021.11.014
|
[15] |
Has C, Bauer JW, Bodemer C, et al. Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility[J]. Br J Dermatol, 2020, 183(4): 614-627. doi: 10.1111/bjd.18921
|
[16] |
Chen F, Wei R, Deng D, et al. Genotype and phenotype correlations in 441 patients with epidermolysis bullosa from China[J]. J Eur Acad Dermatol Venereol, 2023, 37(2): 411-419. doi: 10.1111/jdv.18692
|
[17] |
Chen C, Hou G, Zeng C, et al. Metabolomic profiling reveals amino acid and carnitine alterations as metabolic signatures in psoriasis[J]. Theranostics, 2021, 11(2): 754-767. doi: 10.7150/thno.51154
|
[18] |
Chiu CY, Lin G, Wang CJ, et al. Metabolomics reveals microbial-derived metabolites associated with immunoglobulin E responses in filaggrin-related atopic dermatitis[J]. Pediatr Allergy Immunol, 2021, 32(8): 1709-1717. doi: 10.1111/pai.13570
|
[19] |
Huang Y, Chen G, Liu X, et al. Serum metabolomics study and eicosanoid analysis of childhood atopic dermatitis based on liquid chromatography-mass spectrometry[J]. J Proteome Res, 2014, 13(12): 5715-5723. doi: 10.1021/pr5007069
|
[20] |
Lee SJ, Woo SI, Ahn SH, et al. Functional interpretation of metabolomics data as a new method for predicting long-term side effects: treatment of atopic dermatitis in infants[J]. Sci Rep, 2014, 4: 7408. doi: 10.1038/srep07408
|
[21] |
Xing L, Wu T, Yu L, et al. Exploration of biomarkers of psoriasis through combined multiomics analysis[J]. Mediators Inflamm, 2022, 2022: 7731082.
|
[22] |
Leng L, Liu Z, Ma J, et al. Proteomic identification of new diagnostic biomarkers of early-stage cutaneous mycosis fungoides[J]. Cancer Commun (Lond), 2022, 42(6): 558-562. doi: 10.1002/cac2.12266
|
[23] |
Xu C, Zhou D, Luo Y, et al. Tissue and serum lipidome shows altered lipid composition with diagnostic potential in mycosis fungoides[J]. Oncotarget, 2017, 8(29): 48041-48050. doi: 10.18632/oncotarget.18228
|
[24] |
Wang L, Yu X, Wu C, et al. RNA sequencing-based longitudinal transcriptomic profiling gives novel insights into the disease mechanism of generalized pustular psoriasis[J]. BMC Med Genomics, 2018, 11(1): 52. doi: 10.1186/s12920-018-0369-3
|
[25] |
弓孟春, 焦塬石, 马武仁, 等. 人工智能支持罕见病诊疗的研究进展[J]. 罕见病研究, 2022, 1(2): 101-109. doi: 10.12376/j.issn.2097-0501.2022.02.003
|
[26] |
Kakkis ED, Muenzer J, Tiller GE, et al. Enzyme-replacement therapy in mucopolysaccharidosis I[J]. N Engl J Med, 2001, 344(3): 182-188. doi: 10.1056/NEJM200101183440304
|
[27] |
Germain DP, Charrow J, Desnick RJ, et al. Ten-year outcome of enzyme replacement therapy with agalsidase beta in patients with Fabry disease[J]. J Med Genet, 2015, 52(5): 353-358. doi: 10.1136/jmedgenet-2014-102797
|
[28] |
Longhurst H, Cicardi M, Craig T, et al. Prevention of hereditary angioedema attacks with a subcutaneous C1 inhibitor[J]. N Engl J Med, 2017, 376(12): 1131-1140. doi: 10.1056/NEJMoa1613627
|
[29] |
French JA, Lawson JA, Yapici Z, et al. Adjunctive everolimus therapy for treatment-resistant focal-onset seizures associated with tuberous sclerosis (EXIST-3): a phase 3, randomised, double-blind, placebo-controlled study[J]. Lancet, 2016, 388(10056): 2153-2163. doi: 10.1016/S0140-6736(16)31419-2
|
[30] |
Bissler JJ, McCormack FX, Young LR, et al. Sirolimus for angiomyolipoma in tuberous sclerosis complex or lymphangioleiomyomatosis[J]. N Engl J Med, 2008, 358(2): 140-151. doi: 10.1056/NEJMoa063564
|
[31] |
Langendonk JG, Balwani M, Anderson KE, et al. Afamelanotide for erythropoietic protoporphyria[J]. N Engl J Med, 2015, 373(1): 48-59. doi: 10.1056/NEJMoa1411481
|
[32] |
Donadieu J, Larabi IA, Tardieu M, et al. Vemurafenib for refractory multisystem langerhans cell histiocytosis in children: an international observational study[J]. J Clin Oncol, 2019, 37(31): 2857-2865. doi: 10.1200/JCO.19.00456
|
[33] |
Bachelez H, Choon SE, Marrakchi S, et al. Trial of spesolimab for generalized pustular psoriasis[J]. N Engl J Med, 2021, 385(26): 2431-2440. doi: 10.1056/NEJMoa2111563
|
[34] |
Iznardo H, Puig L. Exploring the role of IL-36 cytokines as a new target in psoriatic disease[J]. Int J Mol Sci, 2021, 22(9): 4344.
|
[35] |
Gurevich I, Agarwal P, Zhang P, et al. In vivo topical gene therapy for recessive dystrophic epidermolysis bullosa: a phase 1 and 2 trial[J]. Nat Med, 2022, 28(4): 780-788.
|
[36] |
Leachman SA, Hickerson RP, Schwartz ME, et al. First-in-human mutation-targeted siRNA phase Ib trial of an inherited skin disorder[J]. Mol Ther, 2010, 18(2): 442-446.
|
[37] |
Mendell JR, Rodino-Klapac LR, Sahenk Z, et al. Eteplirsen for the treatment of Duchenne muscular dystrophy[J]. Ann Neurol, 2013, 74(5): 637-647.
|
[38] |
Darras BT, Chiriboga CA, Iannaccone ST, et al. Nusiner-sen in later-onset spinal muscular atrophy: long-term results from the phase 1/2 studies[J]. Neurology, 2019, 92(21): e2492-e2506.
|
[39] |
Ablinger M, Lettner T, Friedl N, et al. Personalized development of antisense oligonucleotides for exon skipping restores type XVⅡ collagen expression in junctional epidermolysis bullosa[J]. Int J Mol Sci, 2021, 22(7): 3326.
|
[40] |
Ma J, Li W, Cao R, et al. Application of an iPSC-derived organoid model for localized scleroderma therapy[J]. Adv Sci (Weinh), 2022, 9(16): e2106075.
|