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1.
Arq Gastroenterol ; 58(2): 214-216, 2021.
Artículo en Inglés | MEDLINE | ID: mdl-34231664

RESUMEN

BACKGROUND: Celiac disease (CD) is an autoimmune disease characterized by immune reaction mostly to wheat gluten. The diagnosis is based on clinical, serological and histological findings in patients ingesting gluten. Cases that the clinical profile indicates CD and the autoantibodies are negative bring so a dilemma for the professional, as the risk of missed the diagnosis or a delay at the same. OBJECTIVE: To show the importance of correct diagnosis of cases with seronegative celiac disease (SNCD). METHODS: Ten cases of SNCD Brazilian patients were retrospectively studied (2013 to 2019). Data of clinical complaints, autoantibodies, IgA serum levels, histological findings and HLA-DQ2/DQ-8 were compiled. Dual-X densitometry, delay at diagnosis, previous autoimmune diseases and family history of CD were also checked. RESULTS: All SNCD patients presented clinical symptoms of CD, with confirmed diagnosis by histological findings of the duodenal mucosa and HLA-DQ2 and/or HLA-DQ8 positivity. All patients had normal IgA levels and negative autoantibodies (IgA-anti-transglutaminase and anti-endomysial). Dual-X densitometry detected osteopenia in two women and osteoporosis in two males, all with low levels of vitamin D. Delay diagnostic ranged from 1 to 19 years. Familiar occurrence of CD was reported in 40% of the cases. After one year of gluten-free diet, eight patients refer improve of symptoms, while duodenal biopsies, done in five cases, showed histological improvement. CONCLUSION: Patients who demonstrate the clinical profile of celiac disease with negative serology and normal levels of IgA, especially those who have family members with celiac disease, should be submitted to duodenal biopsies to look for histological findings.


Asunto(s)
Enfermedad Celíaca , Autoanticuerpos , Enfermedad Celíaca/diagnóstico , Dieta Sin Gluten , Femenino , Glútenes , Humanos , Masculino , Estudios Retrospectivos , Transglutaminasas
2.
Arq. gastroenterol ; 58(2): 214-216, Apr.-June 2021. tab
Artículo en Inglés | LILACS | ID: biblio-1285320

RESUMEN

ABSTRACT BACKGROUND: Celiac disease (CD) is an autoimmune disease characterized by immune reaction mostly to wheat gluten. The diagnosis is based on clinical, serological and histological findings in patients ingesting gluten. Cases that the clinical profile indicates CD and the autoantibodies are negative bring so a dilemma for the professional, as the risk of missed the diagnosis or a delay at the same. OBJECTIVE: To show the importance of correct diagnosis of cases with seronegative celiac disease (SNCD). METHODS: Ten cases of SNCD Brazilian patients were retrospectively studied (2013 to 2019). Data of clinical complaints, autoantibodies, IgA serum levels, histological findings and HLA-DQ2/DQ-8 were compiled. Dual-X densitometry, delay at diagnosis, previous autoimmune diseases and family history of CD were also checked. RESULTS: All SNCD patients presented clinical symptoms of CD, with confirmed diagnosis by histological findings of the duodenal mucosa and HLA-DQ2 and/or HLA-DQ8 positivity. All patients had normal IgA levels and negative autoantibodies (IgA-anti-transglutaminase and anti-endomysial). Dual-X densitometry detected osteopenia in two women and osteoporosis in two males, all with low levels of vitamin D. Delay diagnostic ranged from 1 to 19 years. Familiar occurrence of CD was reported in 40% of the cases. After one year of gluten-free diet, eight patients refer improve of symptoms, while duodenal biopsies, done in five cases, showed histological improvement. CONCLUSION: Patients who demonstrate the clinical profile of celiac disease with negative serology and normal levels of IgA, especially those who have family members with celiac disease, should be submitted to duodenal biopsies to look for histological findings.


RESUMO CONTEXTO: A doença celíaca (DC) é uma doença autoimune caracterizada por reação imune principalmente ao glúten do trigo. O diagnóstico é baseado em achados clínicos, sorológicos e histológicos em pacientes que ingerem glúten. Casos em que o perfil clínico indica DC e os autoanticorpos são negativos trazem um dilema para o profissional, como o risco de não realizar ou atrasar o diagnóstico da DC. OBJETIVO: Mostrar a importância do diagnóstico correto de casos com doença celíaca soronegativa (DCSN). MÉTODOS: Dez casos de pacientes brasileiros com DCSN foram estudados retrospectivamente (2013 a 2019). Foram compilados dados de queixas clínicas, autoanticorpos, níveis séricos de IgA, achados histológicos e HLA-DQ2 / DQ-8. Densitometria, atraso no diagnóstico, doenças autoimunes prévias e histórico familiar de DC também foram verificados. RESULTADOS: Todos os pacientes com DCSN apresentaram sintomas clínicos de DC, com diagnóstico confirmado por achados histológicos da mucosa duodenal e positividade para HLA-DQ2 e/ou HLA-DQ8. Todos os pacientes apresentavam níveis normais de IgA e autoanticorpos negativos (IgA-anti-transglutaminase e anti-endomisial). A densitometria detectou osteopenia em duas mulheres e osteoporose em dois homens, todos com baixos níveis de vitamina D. O atraso no diagnóstico variou de 1 a 19 anos. A ocorrência familiar de DC foi relatada em 40% dos casos. Após 1 ano de dieta isenta em glúten, oito pacientes referem melhora dos sintomas, enquanto as biópsias duodenais, realizadas em cinco casos, mostraram melhora histológica. CONCLUSÃO: Pacientes que apresentam quadro clínico de doença celíaca com sorologia negativa e níveis normais de IgA, principalmente aqueles que possuem familiares com doença celíaca, devem ser submetidos à biópsia duodenal para pesquisa de achados histológicos.


Asunto(s)
Humanos , Masculino , Femenino , Enfermedad Celíaca/diagnóstico , Autoanticuerpos , Transglutaminasas , Estudios Retrospectivos , Dieta Sin Gluten , Glútenes
3.
Rev Esp Enferm Dig ; 108(2): 84-8, 2016 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-26838490

RESUMEN

BACKGROUND: Osteoporosis (OP) is a metabolic bone illness that may complicate celiac disease (CD). It can lead to devastating consequences because of low bone mass and fragility fractures. PURPOSE: To study the OP prevalence in a group of Brazilian patients with CD and the value of a gluten free diet (GFD). METHODS: Retrospective study of celiac female patients from a single University Center followed with bone densitometries. Results from densitometry made at first visit were compared with a second study after a median time of 5 years. During this period, patients were submitted to a GFD according to orientations from special program training. Calcium and vitamin D were prescribed to those patients who did not reach the minimal daily requirement through diet. RESULTS: Forty-one celiac female patients, mean age 46.1 ± 14.8 years, were included. The prevalence of osteopenia at first visit was 56.1% and that of osteoporosis 29.2%. Osteoporosis was associated with longer disease duration (p = 0.01). The second densitometry was performed in a median time of 5 years (range 1 to 13 years) and disclosed 58.9% osteopenia and 28.2% osteoporosis. The GFD improved bone mass, mainly at (of) spine (comparison of T score with p = 0.03 and of bone mass in g/cm2 with p = 0.02), but it was not sufficient to reduce the number of osteopenic (p = 0.9) and osteoporotic patients (p = 0.4). During the follow up period 25% of osteoporotic patients developed low impact fractures. CONCLUSION: Bone health is notably impaired at baseline in CD patients, especially in those with a diagnostic delay. A GFD modestly improved bone mass density with low impact fractures occurring in one third of patients during the follow up period.


Asunto(s)
Densidad Ósea , Enfermedad Celíaca/dietoterapia , Dieta Sin Gluten , Osteoporosis/prevención & control , Adolescente , Adulto , Anciano , Enfermedades Óseas Metabólicas/diagnóstico , Enfermedades Óseas Metabólicas/epidemiología , Enfermedades Óseas Metabólicas/etiología , Enfermedades Óseas Metabólicas/prevención & control , Brasil , Enfermedad Celíaca/complicaciones , Femenino , Estudios de Seguimiento , Humanos , Persona de Mediana Edad , Osteoporosis/diagnóstico , Osteoporosis/epidemiología , Osteoporosis/etiología , Prevalencia , Estudios Retrospectivos , Adulto Joven
4.
Arq Gastroenterol ; 52(3): 171-5, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-26486281

RESUMEN

BACKGROUND: Restrictions imposed by the gluten-free diet generate large changes in the daily habits of the celiac patient, causing a negative impact on quality of life. OBJECTIVE: This study aimed to evaluate the quality of life of patients with celiac disease on a capital in Southern Brazil. METHODS: Patients older than 18 years were included, with confirmed celiac disease for at least 60 days in the period from June to October 2013. A validated questionnaire, with specific questions to assess the patient's quality of life celiac was applied. A total score ranged from 20 to 100 points; the higher the score, worse quality of life. RESULTS: A total of 103 questionnaires were evaluated, 96 (93.2%) female, with average score 56.6±12.35 (28 to 88 points). The comparison between the questionnaire scores and family income was not significant (P=0.139). Patients diagnosed less than 1 year have poorer quality of life than those with more than 10 years (P=0.063). Patients older than 60 years had better quality of life compared with the younger ones (P=0.04). CONCLUSION: There was no association between quality of life and factors such as family income, length of diet and age at diagnosis. Chronological age greater than 60 years has positively influenced the quality of life of celiac patients.


Asunto(s)
Enfermedad Celíaca/fisiopatología , Calidad de Vida , Adolescente , Adulto , Factores de Edad , Brasil , Enfermedad Celíaca/dietoterapia , Estudios Transversales , Dieta Sin Gluten , Femenino , Humanos , Masculino , Persona de Mediana Edad , Factores Socioeconómicos , Encuestas y Cuestionarios , Factores de Tiempo , Adulto Joven
5.
Arq. gastroenterol ; 52(3): 171-175, July-Sep. 2015. tab, ilus
Artículo en Inglés | LILACS | ID: lil-762866

RESUMEN

BackgroundRestrictions imposed by the gluten-free diet generate large changes in the daily habits of the celiac patient, causing a negative impact on quality of life.ObjetiveThis study aimed to evaluate the quality of life of patients with celiac disease on a capital in Southern Brazil.MethodsPatients older than 18 years were included, with confirmed celiac disease for at least 60 days in the period from June to October 2013. A validated questionnaire, with specific questions to assess the patient’s quality of life celiac was applied. A total score ranged from 20 to 100 points; the higher the score, worse quality of life.ResultsA total of 103 questionnaires were evaluated, 96 (93.2%) female, with average score 56.6±12.35 (28 to 88 points). The comparison between the questionnaire scores and family income was not significant (P=0.139). Patients diagnosed less than 1 year have poorer quality of life than those with more than 10 years (P=0.063). Patients older than 60 years had better quality of life compared with the younger ones (P=0.04).ConclusionThere was no association between quality of life and factors such as family income, length of diet and age at diagnosis. Chronological age greater than 60 years has positively influenced the quality of life of celiac patients.


ContextoRestrições impostas pela dieta isenta em glúten podem gerar grandes mudanças nos hábitos diários do paciente celíaco, causando um impacto negativo na sua qualidade de vida.ObjetivoEste estudo teve como objetivo avaliar a qualidade de vida de pacientes com doença celíaca, em uma capital do Sul do Brasil.MétodosPacientes maiores de 18 anos foram incluídos, com doença celíaca confirmada há mais de 60 dias, no período de junho a outubro de 2013. Um questionário validado, com perguntas específicas para avaliar a qualidade de vida do paciente celíaco foi aplicado. A pontuação total nesse questionário varia entre 20 a 100 pontos; quanto maior a pontuação, pior a qualidade de vida.ResultadosNo total 103 questionários foram avaliados, sendo 96 (93,2%) do sexo feminino, com pontuação média de 56,6±12,35 (28-88 pontos). A comparação entre os escores do questionário e renda familiar não foi significativa (P=0,139). Pacientes diagnosticados há menos de 1 ano, apresentam pior qualidade de vida do que aqueles com mais de 10 anos (P=0,063). Pacientes com mais de 60 anos apresentaram melhor qualidade de vida em comparação com os mais jovens (P=0,04).ConclusãoNão houve associação entre a qualidade de vida e fatores como renda familiar, tempo de dieta e idade no momento do diagnóstico. A idade cronológica superior a 60 anos influenciou positivamente a qualidade de vida de pacientes celíacos.


Asunto(s)
Adolescente , Adulto , Femenino , Humanos , Masculino , Persona de Mediana Edad , Adulto Joven , Enfermedad Celíaca/fisiopatología , Calidad de Vida , Factores de Edad , Brasil , Estudios Transversales , Enfermedad Celíaca/dietoterapia , Dieta Sin Gluten , Factores Socioeconómicos , Encuestas y Cuestionarios , Factores de Tiempo
6.
Digestion ; 91(4): 303-6, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-25925094

RESUMEN

BACKGROUND/AIMS: Arthropathy is the most common extraintestinal manifestation observed in patients with Crohn's disease (CD). The present study aimed to screen rheumatoid arthritis (RA) using anti-CCP antibodies and rheumatoid factor (RF) in CD patients from Southern Brazil. Additionally, the presence of arthralgia and spondyloarthritis (SpA) was evaluated. CD patients, previously diagnosed using clinical data, imaging tests, endoscopic and histological findings, were included consecutively. METHODS: A total of 100 patients participated in the study, of which 60% were female, with a mean age of 41.9 ± 12.04 (16-83 years). As controls, sera from 100 healthy individuals from the same geographic area were analyzed. RESULTS: Arthralgias were present in 55% of the patients, being more frequent in women (65.5%; 36/55), than in males (34.5%). No association was found between arthralgia and the treatment method used. Six patients (6/100) had SpA previously diagnosed. In the CD group, anti-CCP was positive only in one patient, while RF was positive in 7 patients (7%; 7/100). The anti-CCP positive patient (woman, 38 years old, RF positive), fulfilled the ACR criteria and was diagnosed as RA. In the control group, anti-CCP antibodies were detected in 1% (1/100) and RF was positive in 6 of the samples (6%). CONCLUSION: Our data showed low frequency of anti-CCP antibodies and RF in Brazilian patients with CD. Additionally, we found a high prevalence of arthralgia in these patients, with 6% of them diagnosed with SpA.


Asunto(s)
Autoanticuerpos/sangre , Enfermedad de Crohn/sangre , Péptidos Cíclicos/sangre , Factor Reumatoide/sangre , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Artralgia/epidemiología , Artralgia/etiología , Artritis Reumatoide/etiología , Brasil , Enfermedad de Crohn/complicaciones , Enfermedad de Crohn/inmunología , Femenino , Humanos , Masculino , Persona de Mediana Edad , Péptidos Cíclicos/antagonistas & inhibidores , Prevalencia , Factores Sexuales , Espondilitis Anquilosante/etiología , Adulto Joven
7.
Rev. bras. alergia imunopatol ; 30(5): 187-193, set.-out. 2007. ilus, tab
Artículo en Portugués | LILACS | ID: lil-471667

RESUMEN

Objetivo: Fazer levantamento de dados recentes relacionados a aspectos estruturais e biológicos da lectina ligante de manose (MBL), assim como da sua participação na fisiopatogenia de diversas doenças. Fonte de dados: Informações contidas em livros, assim como em periódicos acessados principalmente através do Portal da Capes e Pubmed. Síntese dos dados: A MBL é uma proteína com importante participação no sistema imunológico inato e representa a proteína central da ativação da via das lectinas do complemento. A concentração plasmática da MBL é determinada genetica¬mente e varia significativamente entre os indivíduos. A MBL reconhece unidades de açúcares como N-acetil-glucosamina, manose, N-acetil-manosamina, fucose e glucose na superfície de microorganismos, possibilitando a interação com vírus, bactérias, leveduras, fungos e protozoários, levando à sua opsoni¬zação e fagocitose. Dados recentes mostram que a MBL participa na modulação da inflamação e apoptose ao ligar-se a recep¬tores na superfície de fagócitos. A MBL apresenta papel complexo nas doenças. Sua deficiência tem sido associada a maior susceptibilidade a doenças infecciosas, especialmente por patógenos extracelulares. Por outro lado, altas concentrações de MBL sérica têm sido associadas a infecções por microorganismos intracelulares como Leishmania spp. e M. leprae. Há evidências que a MBL também tem participação em condições co¬mo abortos espontâneos, doenças autoimunes e inflamatórias. A MBL é considerada uma proteína de fase aguda, embora apresente aumentos sé ricos modestos quando comparada à proteína C reativa (PCR). Conclusões: Estudos evidenciam ao longo dos anos a notável influência da MBL na resposta inata do hospedeiro e sua participação nos diferentes processos inflamatórios e infecciosos, respaldados na perspectiva que representa a terapia de reposição dessa proteína.


Asunto(s)
Humanos , Colectinas/genética , Sistema Inmunológico , Enfermedades del Sistema Inmune , Lectina de Unión a Manosa , Proteínas del Sistema Complemento , Técnicas Genéticas , Inmunidad Innata , Estructura Molecular
8.
J. bras. patol. med. lab ; 42(5): 339-343, out. 2006. tab
Artículo en Portugués | LILACS | ID: lil-446488

RESUMEN

OBJETIVO: Determinar as concentrações de hormônio estimulante da tireóide (TSH) e a presença de anticorpos antitireoperoxidase (anti-TPO) em pacientes com síndrome de Down (SD) atendidos no ambulatório do Hospital de Clínicas da Universidade Federal do Paraná. MÉTODOS: Foram incluídos no estudo 72 pacientes com SD, não aparentados e selecionados consecutivamente, com média de idade de 6,15 anos. Oitenta crianças sadias, pareadas com os pacientes, foram utilizadas como controles. Em todas as amostras foram determinadas as concentrações séricas de TSH e de anti-TPO, através do método de dosagem imunométrica. RESULTADOS: Trinta pacientes com SD (42,9 por cento) apresentaram alterações nas concentrações de TSH, sendo que 4,3 por cento tinham valores menores que 0,5æUI/ml e 38,6 por cento, valores superiores a 5æUI/ml (5,1 a 22) (média de 5,56 ± 4,18æUI/ml). Nos controles, a concentração média de TSH foi 2,76æUI/ml (± 1,14), evidenciando-se um aumento significativo nos níveis de TSH nos pacientes com SD (p < 0,001). De forma similar, caracterizou-se uma diferença significativa na positividade para o anti-TPO nos pacientes (15,4 por cento) em relação aos controles (0 por cento; p < 0,001). Observou-se ainda aumento significativo nas concentrações de TSH nos pacientes com idade superior a 9 anos (média de 6,86 ± 4,6æUI/ml) quando comparados aos menores de 9 anos (média de 5,24 ± 3,81æUI/ml; p = 0,006), bem como na positividade do anti-TPO (6/20 vs. 5/52; p = 0,041). CONCLUSÕES: Os resultados demonstraram alta prevalência de alterações das dosagens de TSH e de doença tireoidiana nos pacientes com SD, principalmente naqueles com idade superior a 9 anos. Os dados indicam que a avaliação da função tireoidiana nos pacientes com SD deve receber atenção especial dos profissionais de saúde que atendem esses pacientes.


OBJECTIVE: To evaluate the thyroid stimulating hormone (TSH) levels and the presence of antithyroperoxidase antibody (anti-TPO) in DownÆs syndrome (DS) patients from Hospital de Clínicas of Universidade Federal do Paraná (HC/UFPR). METHODS: Seventy-two DS patients, non-related and consecutively selected (mean age 6.15) were included in the study. Eighty matched healthy children were used as controls. The TSH measurement and the anti-TPO were determined by immunometric assay in all samples. RESULTS: Thirty patients with DS (42.9 percent) presented abnormal levels of TSH; 4.3 percent showed values below 0.5æIU/ml and 38.6 percent presented values higher than 5æIU/ml (range 5.1-22; mean 5.56 ± 4.18æIU/ml). The mean concentration of TSH in the controls was 2.76 ± 1.14æIU/ml, indicating a significant increase in TSH levels in the DS patients (p < 0.001). Similarly, a significant difference was observed in the anti-TPO positivity in the patientsÆ group (15.4 percent) when compared with the controls (0 percent; p < 0.001). In addition, the TSH levels of patients older than 9 years presented a significant increase (mean of 6.86 ± 4.6æIU/ml) when compared with the levels observed in patients younger than 9 years (mean of 5.24 ± 3.81æIU/ml; p = 0.006). The same pattern was observed in the positivity of anti-TPO (6/20 vs. 5/52; p = 0.041). CONCLUSIONS: The results demonstrated high prevalence of elevated TSH and anti-TPO in the patients from the DS ambulatory of HC/UFPR, with increased frequency in those older than 9 years. The data indicate that the evaluation of thyroid function in DS patients must receive special attention from health professionals who take care of these patients.

9.
J Pediatr (Rio J) ; 81(5): 373-6, 2005.
Artículo en Inglés | MEDLINE | ID: mdl-16247538

RESUMEN

OBJECTIVES: High prevalence rates of celiac disease in patients with Down syndrome have been reported in several countries. However, in Brazil there is no data regarding this association. In this study we report the prevalence of celiac disease in Down syndrome children and adolescents from southern Brazil. METHODS: Seventy-one patients (32 female and 39 male, 2-18 years) from Curitiba, Brazil, were studied. Eighty young people (42 male and 38 female, 2-19 years) were used as controls. All subjects were screened for the IgA-antiendomysium antibody (EmA) and IgA anti-tecidual transglutaminase (anti-tTG). EmA was measured by an immunofluorescence assay using umbilical cord as the substrate and anti-tTG by ELISA with tecidual transglutaminase as the antigen. The total IgA serum level was determined by turbidimetry. RESULTS: Five DS patients (7%) were positive for EmA-IgA, with titers from 1/5 to 1/80 and 14 (17.5%) for anti-tTG (21-340 units). All EmA positive patients also presented anti-tTG antibodies simultaneously. Clinical and histological findings of the intestinal mucosa confirmed celiac disease diagnoses in four patients. The other EmA positive patient was asymptomatic and was not submitted to duodenal biopsy. Patients only positive for anti-tTG presented borderline values (< 25 units) and were asymptomatic. None of the controls were positive for EmA or anti-tTG. No Down syndrome patients or controls presented IgA deficiency. CONCLUSIONS: These data indicates a high prevalence (5.6%) of confirmed celiac disease in Down syndrome patients from southern Brazil.


Asunto(s)
Enfermedad Celíaca/epidemiología , Síndrome de Down/complicaciones , Adolescente , Brasil/epidemiología , Estudios de Casos y Controles , Enfermedad Celíaca/complicaciones , Enfermedad Celíaca/inmunología , Niño , Preescolar , Síndrome de Down/inmunología , Ensayo de Inmunoadsorción Enzimática , Femenino , Sangre Fetal/inmunología , Humanos , Inmunoglobulina A/sangre , Masculino , Prevalencia , Transglutaminasas/inmunología
10.
J. pediatr. (Rio J.) ; 81(5): 373-376, set.-out. 2005. tab, graf
Artículo en Portugués | LILACS | ID: lil-418520

RESUMEN

OBJETIVOS: Alta prevalência de doença celíaca em pacientes com síndrome de Down tem sido descrita em vários países. No entanto, no Brasil ainda não há relatos mostrando essa associação. O presente estudo teve como objetivo avaliar a prevalência de doença celíaca em crianças e adolescentes com síndrome de Down no sul do Brasil. MÉTODOS: Setenta e um pacientes (32 do sexo feminino e 39 masculino, 2-18 anos) provenientes de Curitiba, Brasil, foram estudados. Oitenta indivíduos (42 do sexo masculino e 38 feminino, 2-19 anos) foram utilizados como controles do estudo. Todas as amostras foram investigadas para anticorpo anti-endomísio (EmA) e anti-transglutaminase tecidual (anti-tTG). O EmA foi pesquisado através de imunofluorescência indireta usando cordão umbilical como substrato e o anti-tTG através da técnica de ELISA, utilizando transglutaminase tecidual como antígeno. As dosagens de IgA foram realizadas por turbidimetria. RESULTADOS: Cinco pacientes com síndrome de Down (7 por cento) foram positivos para EmA-IgA, com títulos entre 1/5 e 1/80 e catorze (17,5 por cento) para anti-tTG (21-340 unidades). Todos os pacientes positivos para EmA apresentaram simultaneamente positividade para o anti-tTG. Os achados clínicos e histológicos na mucosa intestinal confirmaram doença celíaca em quatro pacientes. O outro paciente EmA positivo não foi submetido a biópsia duodenal. Os pacientes positivos apenas para anti-tTG apresentaram valores limítrofes (< 25 unidades) e eram assintomáticos. Nenhum indivíduo do grupo controle foi positivo para EmA ou anti-tTG. Nenhuma amostra do estudo foi deficiente para IgA. CONCLUSÕES: Os dados do presente estudo mostram alta prevalência (5,6 por cento) de doença celíaca confirmada em crianças e adolescentes com síndrome de Down da região sul do Brasil.


Asunto(s)
Adolescente , Niño , Preescolar , Femenino , Humanos , Masculino , Enfermedad Celíaca/epidemiología , Síndrome de Down/complicaciones , Brasil/epidemiología , Estudios de Casos y Controles , Enfermedad Celíaca/complicaciones , Enfermedad Celíaca/inmunología , Síndrome de Down/inmunología , Ensayo de Inmunoadsorción Enzimática , Sangre Fetal/inmunología , Inmunoglobulina A/sangre , Prevalencia , Transglutaminasas/inmunología
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