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1.
Clin Genet ; 106(5): 644-649, 2024 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-39015008

RESUMEN

Limb-girdle muscular dystrophy type 2G/R7 (LGMD2G/R7) is an ultra-rare condition initially identified within the Brazilian population. We aimed to expand clinical and genetic information about this disease, including its worldwide distribution. A multicenter historical cohort study was performed at 13 centers in Brazil in which data from index cases and their affected relatives from consecutive families with LGMD2G/R7 were reviewed from July 2017 to August 2023. Additionally, a systematic literature review was conducted to identify case reports and series of the disease worldwide. Forty-one LGMD2G/R7 cases were described in the Brazilian cohort, being all subjects homozygous for the c.157C>T/(p.Gln53*) variant in TCAP. Survival curves showed that the median disease duration before individuals required walking aids was 21 years. Notably, women exhibited a slower disease progression, requiring walking aids 13 years later than men. LGMD2G/R7 was frequently reported not only in Brazil but also in China and Bulgaria, with 119 cases identified globally, with possible founder effects in the Brazilian, Eastern European, and Asian populations. These findings are pivotal in raising awareness of LGMD2G/R7, understanding its progression, and identifying potential modifiers. This can significantly contribute to the development of future natural history studies and clinical trials for this disease.


Asunto(s)
Distrofia Muscular de Cinturas , Mutación , Humanos , Distrofia Muscular de Cinturas/genética , Distrofia Muscular de Cinturas/epidemiología , Distrofia Muscular de Cinturas/diagnóstico , Masculino , Brasil/epidemiología , Femenino , Adulto , Adolescente , Persona de Mediana Edad , Niño , Estudios de Cohortes , Adulto Joven , Linaje , Conectina/genética , Fenotipo , Predisposición Genética a la Enfermedad , Preescolar
2.
Transpl Infect Dis ; 19(4)2017 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-28306183

RESUMEN

Serological diagnosis of flavivirus infection is a challenge, particularly in the context of a disease associated with immune response enhancement in a transplant patient, where aspects such as previous flavivirus infections may be involved with the outcome. We report a case of a pediatric patient who developed Guillain-Barré syndrome (GBS) after matched-unrelated hematopoietic stem cell transplantation (HSCT). The patient lives in a Brazilian region that is experiencing an epidemic of Zika virus (ZIKV) and dengue virus (DENV). Because an increasing number of cases of GBS, likely triggered by ZIKV infection, are being reported in Brazil, samples from the patient were tested for both ZIKV and DENV infection. Serological assays strongly suggested a recent ZIKV infection, although infection by DENV or co-infection with both viruses cannot be ruled out. The presence of anti-DENV immunoglobulin-G in donor serum led to the hypothesis that antibodies from the donor could have enhanced the severity of the ZIKV infection. This hypothesis is in agreement with the recent findings that DENV sero-cross-reactivity drives antibody-dependent enhancement of ZIKV infection. These findings highlight the need for discussion of the indication to perform previous flavivirus tests in HSCT donors, especially in areas where ZIKV and other flaviviruses co-circulate.


Asunto(s)
Virus del Dengue/inmunología , Dengue/complicaciones , Síndrome de Guillain-Barré/etiología , Trasplante de Células Madre Hematopoyéticas/efectos adversos , Infección por el Virus Zika/complicaciones , Virus Zika/inmunología , Anticuerpos Antivirales/sangre , Brasil , Niño , Coinfección , Reacciones Cruzadas , Dengue/diagnóstico , Dengue/virología , Femenino , Síndrome de Guillain-Barré/diagnóstico , Síndrome de Guillain-Barré/inmunología , Humanos , Inmunoglobulina M/sangre , Pruebas Serológicas , Infección por el Virus Zika/diagnóstico , Infección por el Virus Zika/virología
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