Prevalence of lymphedema among Anderson-Fabry disease patients: A report from the Fabry registry
Tài liệu tham khảo
Adeboye, 2022, The cardiovascular manifestations of Anderson-Fabry disease, Curr. Cardiovasc. Risk Rep., 16, 43, 10.1007/s12170-022-00691-1
Zarate, 2008, Fabry’s disease, Lancet., 372, 1427, 10.1016/S0140-6736(08)61589-5
Tuttolomondo, 2013, Anderson-Fabry disease: a multiorgan disease, Curr. Pharm. Des., 19, 5974, 10.2174/13816128113199990352
Giuseppe, 2013, Cutaneous complications of Anderson-Fabry disease, Curr. Pharm. Des., 19, 6031, 10.2174/13816128113199990359
Hopkin, 2008, Characterization of Fabry disease in 352 pediatric patients in the Fabry registry, Pediatr. Res., 64, 550, 10.1203/PDR.0b013e318183f132
Orteu, 2007, Fabry disease and the skin: data from FOS, the Fabry outcome survey, Br. J. Dermatol., 157, 331, 10.1111/j.1365-2133.2007.08002.x
Desnick, 2003, Fabry disease, an under-recognized multisystemic disorder: expert recommendations for diagnosis, management, and enzyme replacement therapy, Ann. Intern. Med., 138, 338, 10.7326/0003-4819-138-4-200302180-00014
Wise, 1962, Angiokeratoma corporis diffusum. A clinical study of eight affected families, Q. J. Med., 31, 177
MacDermot, 2001, Anderson-Fabry disease: clinical manifestations and impact of disease in a cohort of 98 hemizygous males, J. Med. Genet., 38, 750, 10.1136/jmg.38.11.750
Whybra, 2001, Anderson-Fabry disease: clinical manifestations of disease in female heterozygotes, J. Inherit. Metab. Dis., 24, 715, 10.1023/A:1012993305223
MacDermot, 2001, Anderson-Fabry disease: clinical manifestations and impact of disease in a cohort of 60 obligate carrier females, J. Med. Genet., 38, 769, 10.1136/jmg.38.11.769
Galanos, 2002, Clinical features of Fabry’s disease in Australian patients, Intern. Med. J., 32, 575, 10.1046/j.1445-5994.2002.00291.x
Amann-Vesti, 2003, Severe lymphatic microangiopathy in Fabry disease, Lymphat. Res. Biol., 1, 185, 10.1089/153968503768330229
Lidove, 2016, Musculoskeletal manifestations of Fabry disease: a retrospective study, Joint Bone Spine., 83, 421, 10.1016/j.jbspin.2015.11.001
Fabry Disease Registry
Saito, 2011, Fabry-database.org: database of the clinical phenotypes, genotypes and mutant α-galactosidase A structures in Fabry disease, J. Hum. Genet., 56, 467, 10.1038/jhg.2011.31
Rockson, 2008, Diagnosis and management of lymphatic vascular disease, J. Am. Coll. Cardiol., 52, 799, 10.1016/j.jacc.2008.06.005