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1.
Consenso de leucemia mieloide aguda en México
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Arana-Luna, Luara L.
; Alvarado-Ibarra, Martha
; Silva-Michel, Luis G.
; Morales-Maravilla, Adrián
; González-Rubio, María del C.
; Chávez-Aguilar, Lénica A.
; Tena-Iturralde, María Fernanda
; Mojica-Balceras, Liliana
; Zapata-Canto, Nidia
; Galindo-Delgado, Patricia
; Miranda-Madrazo, María Raquel
; Morales-Hernández, Alba E.
; Silva-Vera, Karina
; Grimaldo-Gómez, Flavio A.
; Hernández-Caballero, Álvaro
; Bates-Martin, Ramón A.
; Álvarez-Vera, José L.
; Tepepa-Flores, Fredy
; Teomitzi-Sánchez, Óscar
; Fermín-Caminero, Denisse J.
; Peña-Celaya, José A. de la
; Salazar-Ramírez, Óscar
; Flores-Villegas, Luz V.
; Guerra-Alarcón, Lidia V.
; Leyto-Cruz, Faustino
; Inclán-Alarcón, Sergio I.
; Milán-Salvatierra, Andrea I.
; Ventura-Enríquez, Yanet
; Pérez-Lozano, Uendy
; Báez-Islas, Pamela E.
; Tapia-Enríquez, Ana L.
; Palma-Moreno, Orlando G.
; Aguilar-Luévano, Jocelyn
; Espinosa-Partida, Arturo
; Pérez-Jacobo, Luis F.
; Rojas-Castillejos, Flavio
; Ruiz-Contreras, Josué I.
; Loera-Fragoso, Sergio J.
; Medina-Coral, Jesús E.
; Acosta-Maldonado, Brenda L.
; Soriano-Mercedes, Emely J.
; Saucedo-Montes, Erick E.
; Valero-Saldana, Luis M.
; González-Prieto, Susana G.
; Nava-Villegas, Lorena
; Hernández-Colin, Ana K.
; Hernández-Alcántara, Areli E.
; Zárate-Rodríguez, Pedro A.
; Ignacio-Ibarra, Gregorio
; Meillón-García, Luis A.
; Espinosa-Bautista, Karla A.
; Ledesma de la Cruz, Cindy
; Barbosa-Loría, Diego M.
; García-Castillo, Carolina
; Balderas-Delgado, Carolina
; Cabrera-García, Álvaro
; Pérez-Zúñiga, Juan M.
; Hernández-Ruiz, Eleazar
; Villela-Peña, Atenas
; Gómez Cortés, Sue Cynthia
; Romero-Rodelo, Hilda
; Garzón-Velásquez, Katheryn B.
; Serrano-Hernández, Cristina
; Martínez-Ríos, Annel
; Pedraza-Solís, María Luisa
; Martínez-Coronel, Jorge A.
; Narváez-Davalos, Iris M.
; García-Camacho, Alinka S.
; Merino-Pasaye, Laura E.
; Aguilar-Andrade, Carolina
; Aguirre-Domínguez, Juan A.
; Guzmán-Mera, Pedro G.
; Delgado-de la Rosa, Elizabeth
; Flores López, Perla E.
; González-Aguirre, Lilia L.
; Ramírez-Alfaro, Edgar M.
; Vera-Calderón, Heidi
; Meza-Dávalos, María Lizeth
; Murillo-Cruz, Juan
; Pichardo-Cepín, Yayra M.
; Ramírez-Romero, Eva F.
.
Abstract Acute myeloid leukemia (AML) comprises a heterogeneous group of hematopoietic cell neoplasms of myeloid lineage that arise from the clonal expansion of their precursors in the bone marrow, interfering with cell differentiation, leading to a syndrome of bone marrow failure. AML is a consequence of genetic and epigenetic changes (point mutations, gene rearrangements, deletions, amplifications, and arrangements in epigenetic changes that influence gene expression) in hematopoietic precursor cells, which create a clone of abnormal cells that are capable of proliferating but cannot differentiate into mature hematopoietic cells or undergo programmed cell death. The diagnosis requires more than 20% myeloid blasts in the bone marrow and certain cytogenic abnormalities. Treatment will depend on age, comorbidities, and cytogenetic risk among the most frequent.
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https://doi.org/10.24875/gmm.m21000597
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2.
Guía de práctica clínica mexicana para el diagnóstico y tratamiento de las dislipidemias y enfermedad cardiovascular aterosclerótica
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Pavía-López, Abel A.
; Alcocer-Gamba, Marco A.
; Ruiz-Gastelum, Edith D.
; Mayorga-Butrón, José L.
; Mehta, Roopa
; Díaz-Aragón, Filiberto A.
; Aldrete-Velasco, Jorge A.
; López-Juárez, Nitzia
; Cruz-Bautista, Ivette
; Chávez-Mendoza, Adolfo
; Secchi-Nicolás, Nikos C.
; Guerrero-Martínez, Francisco J.
; Cossio-Aranda, Jorge E.
; Mendoza-Zubieta, Victoria
; Fanghänel-Salmon, Guillermo
; Valdivia-Proa, Martha
; Olmos-Domínguez, Luis
; Aguilar-Salinas, Carlos A.
; Dávila-Maldonado, Luis
; Vázquez-Rangel, Armando
; Pavia-Aubry, Vanina
; Nava-Hernández, María de los A.
; Hinojosa-Becerril, Carlos A.
; Anda-Garay, Juan C.
; Ríos-Ibarra, Manuel O. de los
; Berni-Betancourt, Ana C.
; López-Cuellar, Julio
; Araiza-Garaygordobil, Diego
; Rivera-Reyes, Romina
; Borrayo-Sánchez, Gabriela
; Tapia-Hernández, Mónica
; Cano-Nigenda, Claudia V.
; Guerra-López, Arturo
; Elías-López, Josué
; Figueroa-Morales, Marco A.
; Montaño-Velázquez, Bertha B.
; Velasco-Hidalgo, Liliana
; Rodríguez-Lozano, Ana L.
; Pimentel-Hernández, Claudia
; Baquero-Hoyos, María M.
; Romero-Moreno, Felipe
; Rodríguez-Vega, Mario
.
resumen está disponible en el texto completo
Abstract Background: Cardiovascular diseases are the leading cause of mortality worldwide and Mexico is no exception. The epidemiological data obtained in 1990 showed that cardiovascular diseases represented 19.8% of all causes of death in our country. This figure increased significantly to 25.5% for 2015. Some national surveys suggest that more than 60% of the adult population has at least one risk factor for cardiovascular disease (obesity or overweight, hypertension, smoking, diabetes, dyslipidemias). On the other hand, data from the Pan American Health Organization have linked the process of atherosclerosis as the first cause of premature death, significantly reducing life expectancy, which has enormous social repercussions. Objective: This document constitutes the Clinical Practice Guide (CPG) prepared at the initiative of the Mexican Society of Cardiology in collaboration with the Mexican Society of Nutrition and Endocrinology, AC, National Association of Cardiologists of Mexico, AC, Mexican Association for the Prevention of Atherosclerosis and its Complications, AC, National Normative Committee of General Medicine, AC, National College of Geriatric Medicine, AC, College of Internal Medicine of Mexico, AC, Mexican Society of Angiology and Vascular and Endovenous Surgery, AC, Mexican Institute of Research Nephrological, AC and the Mexican Academy of Neurology, A.C.; with the methodological support of the Ibero-American Agency for the Development and Evaluation of Health Technologies, in order to establish recommendations based on the best available evidence and agreed upon by an interdisciplinary group of experts. The objective of this document is to provide evidence-based recommendations to help decision makers in the diagnosis and treatment of dyslipidemias in our country. Material and methods: This document complies with international quality standards, such as those described by the Institute of Medicine of the USA, the Institute of Clinical Excellence of Great Britain, the Scottish Intercollegiate Guideline Network and the Guidelines International Network. A multidisciplinary group of clinical experts and methodologists with experience in systematic reviews of the literature and the development of clinical practice guidelines was formed. A scope document was agreed upon, relevant clinical questions were established, the best available evidence critically evaluated in systematic literature reviews was exhaustively identified, and clinical recommendations were developed. The modified Delphi Panel methodology was used to achieve an adequate level of consensus in each of the recommendations contained in this CPG. Results: 23 clinical questions were agreed upon which gave rise to their respective clinical recommendations. Conclusions: We consider that this document contributes to better clinical decision-making and becomes a point of reference for clinicians and patients in the management of dyslipidemias and this contributes to reducing the morbidity and mortality derived from atherosclerotic cardiovascular events in our country.
https://doi.org/10.24875/acm.m22000081
1458 downloads
3.
Consenso de hemofilia en México
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López-Arroyo, José L.
; Pérez-Zúñiga, Juan M.
; Merino-Pasaye, Laura E.
; Saavedra-González, Azucena
; Alcivar-Cedeño, Luisa María
; Álvarez-Vera, José Luis
; Anaya-Cuellar, Irene
; Arana-Luna, Luara L.
; Ávila-Castro, David
; Bates-Martín, Ramón A.
; Cesarman-Maus, Gabriela
; Chávez-Aguilar, Lénica A.
; Peña-Celaya, José A. de la
; Espitia-Ríos, María E.
; Estrada-Domínguez, Patricia
; Fermín-Caminero, Denisse
; Flores-Patricio, Willy
; García Chávez, Jaime
; García-Lee, María T.
; González-Pérez, María del Carmen
; González-Rubio, María del Carmen
; González-Villareal, María Guadalupe
; Ramírez-Moreno, Fabiola
; Hernández-Colin, Ana K.
; Hernández-Ruiz, Eleazar
; Herrera-Olivares, Wilfrido
; Leyto-Cruz, Faustino
; Loera-Fragoso, Sergio
; Martínez-Ríos, Annel
; Miranda-Madrazo, María R.
; Morales-Hernández, Alba
; Nava-Villegas, Lorena
; Orellana-Garibay, Juan J.
; Palma-Moreno, Orlando G.
; Paredes-Lozano, Eugenia P.
; Peña-Alcántara, Paula
; Pérez-Lozano, Uendy
; Pichardo-Cepín, Yayra M.
; Reynoso-Pérez, Ana Carolina
; Rodríguez-Serna, Mishel
; Rojas-Castillejos, Flavio
; Romero-Rodelo, Hilda
; Ruíz-Contreras, Josué I.
; Segura-García, Adela
; Silva-Vera, Karina
; Soto-Cisneros, Paulina M.
; Tapia-Enríquez, Ana L.
; Tavera-Rodríguez, Martha G.
; Teomitzi-Sánchez, Óscar
; Tepepa-Flores, Fredy
; Valencia-Rivas, María D.
; Valle-Cárdenas, Teresa
; Varela-Constantino, Ana
; Javier-Morales, Adrián
; Martínez-Ramírez, Mario A.
; Tena-Cano, Sergio
; Terrazas-Marín, Ricardo
; Vilchis-González, Shendel P.
; Villela-Peña, Atenas
; Mena-Zepeda, Verónica
; Alvarado Ibarra, Martha
.
Abstract Hemophilia is a hemorrhagic disorder with a sex-linked inherited pattern, characterized by an inability to amplify coagulation due to a deficiency in coagulation factor VIII (hemophilia A or classic) or factor IX (hemophilia B). Sequencing of the genes involved in hemophilia has provided a description and record of the main mutations, as well as a correlation with the various degrees of severity. Hemorrhagic manifestations are related to levels of circulating factor, mainly affecting the musculoskeletal system and specifically the large joints (knees, ankles and elbows). This document is a review and consensus of the main genetic aspects of hemophilia, from the inheritance pattern to the concept of women carriers, physiopathology and classification of the disorder, the basic and confirmation studies when hemophilia is suspected, the various treatment regimens based on infusion of the deficient coagulation factor as well as innovative factor-free therapies and recommendations for the management of complications associated with treatment (development of inhibitors and/or transfusion transmitted infections) or secondary to articular hemorrhagic events (hemophilic arthropathy). Finally, relevant reviews of clinical and treatment aspects of hemorrhagic pathology charachterized by acquired deficiency of FVIII secondary to neutralized antibodies named acquired hemophilia.
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https://doi.org/10.24875/gmm.m20000451
305 downloads
4.
Consenso Mexicano de Mieloma Múltiple
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Peña-Celaya, José A. de la
; Aguilar-Luevano, Jocelyn
; Alcivar-Cedeño, Luisa María
; Álvarez-Vera, José L.
; Anaya-Cuellar, Irene
; Añorve-Hernández, Erika
; Arana-Luna, Luara L.
; Arteaga-Ortíz, Luis
; Báez-Islas, Pamela E.
; Banda-García, Luisa I.
; Bates-Martín, Ramón A.
; Campa-Monroy, Dafne Itzel
; Cardiel-Silva, Mariela
; Castillo-Salas, Ángel de Jesús
; Cota-Rangel, Xóchitl
; Díaz-Vargas, Guillermo
; Espitia-Ríos, M. Eugenia
; Estrada-Domínguez, Patricia
; Fermín-Caminero, Denisse
; García-Camacho, Alinka
; García-Castillo, Carolina
; Garzón-Velásquez, Katheryn B.
; Gil-Rondero, Carlos
; Hernández-Colín, Ana K.
; Hernández-Ruiz, Eleazar
; Hernández-Alcántara, Areli E.
; Hernández-Cervantes, Silvia A.
; Herrera-Olivares, Wilfrido
; Ignacio-Ibarra, Gregorio
; Inclán-Alarcón, Sergio I.
; Leyto-Cruz, Faustino
; Macías-Flores, Juan P.
; Martínez-de la Vega, Andrea
; Martínez-Ramírez, Mario A.
; Martínez-Coronel, Jorge
; Medina-Coral, Jesús E.
; Meza-Dávalos, Lizeth
; Montoya-Jiménez, Leire
; Morales-Hernández, Alba
; Morales-López, Elizabeth
; Morales-Adrián, Javier de Jesús
; Morales-de Azcué, Maricruz
; Mújica-Martínez, Aldo
; Murillo-Cruz, Juan L.
; Nájera-Martínez, Jéssica
; Narváez-Sarmiento, Iris M.
; Nava-Villegas, Lorena
; Nava-Alpide, Marco A.
; Orellana-Garibay, Juan J.
; Palafox-Zaldívar, María Teresa
; Palma-Moreno, Orlando G.
; Paredes-Lozano, Eugenia P.
; Pedraza-Colín, María Luisa
; Pérez-Zúñiga, Juan M.
; Pérez-Lizardi, Alejandra B.
; Rojas-Castillejos, Flavio
; Romero-Martínez, Eduardo
; Romero-Rodelo, Hilda
; Ruiz-Contreras, Josué
; Saavedra-González, Azucena
; Saucedo-Montes, Erick
; Silva-Michel, Luis G.
; Silva-Vera, Karina
; Teomitzi-Sánchez, Óscar
; Tepepa-Flores, Fredy
; Ventura-Enríquez, Yanet
; Villela-Peña, Atenas
; Vilchis-González, Shendel P.
; Zapata-Canto, Nidia
; Zárate-Rodríguez, Pedro A.
; Alvarado-Ibarra, Martha
.
Abstract To identify this increasingly common pathology, known as Multiple Myeloma, it is necessary to refer to the specific factors that characterize it; to this end, the classic criteria known as CRAB (hypercalcemia, renal failure, anemia and lytic lesions) are available, in which renal failure is one of the most frequent complications. Recently, 3 indisputable biomarkers have been described for the diagnostic support for Multiple Myeloma, which are: more than 10% of clonal plasma cells in BM or, a biopsy that corroborates the presence of a plasmacytoma, light chain ratio ≥100 mg/dL and more than one focal lesion on magnetic resonance imaging (MRI). A differential diagnosis for plasma cell leukemia, solitary bone plasmacytoma, and extramedullary plasmacytoma should always be considered. Being this an incurable disease, a lot of research has been done regarding its therapeutic management, whose main objective is the disappearance of plasma cells and the patient clinical improvement. Melphalan was the first drug that showed a benefit in 1958 and afterwards, with the addition of a steroid as a second drug, it was possible to improve response rates. Subsequently, different molecules were studied, forming multiple combinations, and achieving better rates of Overall Survival and Progression-Free Survival. Years later, with the arrival of proteasome inhibitors such as bortezomib, and immunomodulators such as thalidomide and lenalidomide, an important turnaround in the disease has been seen, as deeper responses, more prolonged remissions, and improvement in the quality of life of patients have been achieved. This consensus has the purpose of integrating a group of Mexican specialists and promoting the updating of this pathology.
resumen está disponible en el texto completo
https://doi.org/10.24875/gmm.m20000392
223 downloads
5.
Confiabilidad de los estudios de neuroconducción en el síndrome de túnel carpiano
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ABSTRACT Objective To determine the reliability of neuroconduction studies by comparing two observers and detecting minimum changes when diagnosing carpal tunnel syndrome. Methods Sixty-nine patients referred for electrophysiological study due to suspected carpal tunnel syndrome were studied. The patients underwent two examinations, performed by two evaluators, on two different days. Sensory and motor latencies of the median and ulnar nerves were evaluated; all were classified as negative, incipient, mild, moderate, severe or extreme. Relative interval variation, intraclass correlation coefficient, kappa index, limit of agreement and minimum detectable change were estimated. Results The relative variation of motor nerve latency of the median nerve was -6.8% to 15.9%, with intraclass correlation coefficient of 0.98 for the difference of median-ulnar nerve latency. The minimum detected change was 0.4ms, while the relative interval variation of sensory latency of the median nerve was -5.0% to 11%, with intraclass correlation coefficient of 0.95 for difference with the ulnar nerve. The minimum detectable change was 0.2ms. Electrophysiological classification agreed in 93% of the cases, with a kappa index of 0.89. Conclusions Sensory and motor latencies of the median nerve, as well as the difference between them and the ulnar nerve, are reliable measures. The minimum detectable change obtained in our study helps clinicians to establish whether changes in latencies in consecutive or post-treatment studies are significant.
RESUMEN Objetivo Determinar la confiabilidad entre dos observadores y el cambio mínimo detectable de los estudios de neuroconducción para diagnosticar el síndrome de túnel carpiano. Métodos Se estudiaron 69 pacientes remitidos para estudio electrofisiológico por sospecha de síndrome de túnel carpiano. A los pacientes, se les realizaron dos exámenes, dos días diferentes, por dos evaluadores. Se evaluaron las latencias sensitivas y motoras de los nervios mediano y cubital; todos fueron clasificados como negativos, incipientes, leves, moderados, severos o extremos. Se calculó la variación relativa entre ensayos, el coeficiente de correlación intraclase, el índice de kappa, el límite de acuerdo y el cambio mínimo detectable. Resultados La variación relativa entre ensayos de la latencia motora del nervio mediano fue de -6,8 % a 15,9 % con coeficiente de correlación intraclase de 0,98 para la diferencia con la latencia del nervio cubital. El cambio mínimo detectable fue de 0,4ms. La variación relativa entre ensayos de la latencia sensitiva del nervio mediano fue -5,0 % a 11 % con coeficiente de correlación intraclase de 0,95 para la diferencia con el nervio cubital. El cambio mínimo detectable fue de 0,2ms. La clasificación ele trofisiológica coincidió en 93 % de los casos, índice de kappa de 0,89. Conclusiones Las latencias sensitivas y motoras del nervio mediano así como la diferencia de estas con el nervio cubital son medidas confiables. El cambio mínimo detectable obtenido en nuestro estudio le sirve al clínico para establecer si los cambios de las latencias en estudios consecutivos o después del tratamiento son significativos.
https://doi.org/10.15446/rsap.v19n4.64307
21 downloads
6.
Confiabilidad de los estudios de neuroconducción en el síndrome de túnel carpiano
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RESUMEN Objetivo Determinar la confiabilidad entre dos observadores y el cambio mínimo detectable de los estudios de neuroconducción para diagnosticar el síndrome de túnel carpiano. Métodos Se estudiaron 69 pacientes remitidos para estudio electrofisiológico por sospecha de síndrome de túnel carpiano. A los pacientes, se les realizaron dos exámenes, dos días diferentes, por dos evaluadores. Se evaluaron las latencias sensitivas y motoras de los nervios mediano y cubital; todos fueron clasificados como negativos, incipientes, leves, moderados, severos o extremos. Se calculó la variación relativa entre ensayos, el coeficiente de correlación intraclase, el índice de kappa, el límite de acuerdo y el cambio mínimo detectable. Resultados La variación relativa entre ensayos de la latencia motora del nervio mediano fue de -6,8 % a 15,9 % con coeficiente de correlación intraclase de 0,98 para la diferencia con la latencia del nervio cubital. El cambio mínimo detectable fue de 0,4ms. La variación relativa entre ensayos de la latencia sensitiva del nervio mediano fue -5,0 % a 11 % con coeficiente de correlación intraclase de 0,95 para la diferencia con el nervio cubital. El cambio mínimo detectable fue de 0,2ms. La clasificación ele trofisiológica coincidió en 93 % de los casos, índice de kappa de 0,89. Conclusiones Las latencias sensitivas y motoras del nervio mediano así como la diferencia de estas con el nervio cubital son medidas confiables. El cambio mínimo detectable obtenido en nuestro estudio le sirve al clínico para establecer si los cambios de las latencias en estudios consecutivos o después del tratamiento son significativos.
ABSTRACT Objective To determine the reliability of neuroconduction studies by comparing two observers and detecting minimum changes when diagnosing carpal tunnel syndrome. Methods Sixty-nine patients referred for electrophysiological study due to suspected carpal tunnel syndrome were studied. The patients underwent two examinations, performed by two evaluators, on two different days. Sensory and motor latencies of the median and ulnar nerves were evaluated; all were classified as negative, incipient, mild, moderate, severe or extreme. Relative interval variation, intraclass correlation coefficient, kappa index, limit of agreement and minimum detectable change were estimated. Results The relative variation of motor nerve latency of the median nerve was -6.8% to 15.9%, with intraclass correlation coefficient of 0.98 for the difference of median-ulnar nerve latency. The minimum detected change was 0.4ms, while the relative interval variation of sensory latency of the median nerve was -5.0% to 11%, with intraclass correlation coefficient of 0.95 for difference with the ulnar nerve. The minimum detectable change was 0.2ms. Electrophysiological classification agreed in 93% of the cases, with a kappa index of 0.89. Conclusions Sensory and motor latencies of the median nerve, as well as the difference between them and the ulnar nerve, are reliable measures. The minimum detectable change obtained in our study helps clinicians to establish whether changes in latencies in consecutive or post-treatment studies are significant.
https://doi.org/10.15446/rsap.v19n4.64307
1161 downloads
7.
Growing knowledge: an overview of Seed Plant diversity in Brazil
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Zappi, Daniela C.
; Filardi, Fabiana L. Ranzato
; Leitman, Paula
; Souza, Vinícius C.
; Walter, Bruno M.T.
; Pirani, José R.
; Morim, Marli P.
; Queiroz, Luciano P.
; Cavalcanti, Taciana B.
; Mansano, Vidal F.
; Forzza, Rafaela C.
; Abreu, Maria C.
; Acevedo-Rodríguez, Pedro
; Agra, Maria F.
; Almeida Jr., Eduardo B.
; Almeida, Gracineide S.S.
; Almeida, Rafael F.
; Alves, Flávio M.
; Alves, Marccus
; Alves-Araujo, Anderson
; Amaral, Maria C.E.
; Amorim, André M.
; Amorim, Bruno
; Andrade, Ivanilza M.
; Andreata, Regina H.P.
; Andrino, Caroline O.
; Anunciação, Elisete A.
; Aona, Lidyanne Y.S.
; Aranguren, Yani
; Aranha Filho, João L.M.
; Araújo, Andrea O.
; Araújo, Ariclenes A.M.
; Araújo, Diogo
; Arbo, María M.
; Assis, Leandro
; Assis, Marta C.
; Assunção, Vivian A.
; Athiê-Souza, Sarah M.
; Azevedo, Cecilia O.
; Baitello, João B.
; Barberena, Felipe F.V.A.
; Barbosa, Maria R.V.
; Barros, Fábio
; Barros, Lucas A.V.
; Barros, Michel J.F.
; Baumgratz, José F.A.
; Bernacci, Luis C.
; Berry, Paul E.
; Bigio, Narcísio C.
; Biral, Leonardo
; Bittrich, Volker
; Borges, Rafael A.X.
; Bortoluzzi, Roseli L.C.
; Bove, Cláudia P.
; Bovini, Massimo G.
; Braga, João M.A.
; Braz, Denise M.
; Bringel Jr., João B.A.
; Bruniera, Carla P.
; Buturi, Camila V.
; Cabral, Elza
; Cabral, Fernanda N.
; Caddah, Mayara K.
; Caires, Claudenir S.
; Calazans, Luana S.B.
; Calió, Maria F.
; Camargo, Rodrigo A.
; Campbell, Lisa
; Canto-Dorow, Thais S.
; Carauta, Jorge P.P.
; Cardiel, José M.
; Cardoso, Domingos B.O.S.
; Cardoso, Leandro J.T.
; Carneiro, Camila R.
; Carneiro, Cláudia E.
; Carneiro-Torres, Daniela S.
; Carrijo, Tatiana T.
; Caruzo, Maria B.R.
; Carvalho, Maria L.S.
; Carvalho-Silva, Micheline
; Castello, Ana C.D.
; Cavalheiro, Larissa
; Cervi, Armando C.
; Chacon, Roberta G.
; Chautems, Alain
; Chiavegatto, Berenice
; Chukr, Nádia S.
; Coelho, Alexa A.O.P.
; Coelho, Marcus A.N.
; Coelho, Rubens L.G.
; Cordeiro, Inês
; Cordula, Elizabeth
; Cornejo, Xavier
; Côrtes, Ana L.A.
; Costa, Andrea F.
; Costa, Fabiane N.
; Costa, Jorge A.S.
; Costa, Leila C.
; Costa-e-Silva, Maria B.
; Costa-Lima, James L.
; Cota, Maria R.C.
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Resumo Um levantamento atualizado das plantas com sementes e análises relevantes acerca desta biodiversidade são apresentados. Este trabalho se iniciou em 2010 com a publicação do Catálogo de Plantas e Fungos e, desde então vem sendo atualizado por mais de 430 especialistas trabalhando online. O Brasil abriga atualmente 32.086 espécies nativas de Angiospermas e 23 espécies nativas de Gimnospermas e estes novos dados mostram um aumento de 3% da riqueza em relação a 2010. A Amazônia é o Domínio Fitogeográfico com o maior número de espécies de Gimnospermas, enquanto que a Floresta Atlântica possui a maior riqueza de Angiospermas. Houve um crescimento considerável no número de espécies e nas taxas de endemismo para a maioria dos Domínios (Caatinga, Cerrado, Floresta Atlântica, Pampa e Pantanal), com exceção da Amazônia que apresentou uma diminuição de 2,5% de endemicidade. Entretanto, a maior parte das plantas com sementes que ocorrem no Brasil (57,4%) é endêmica deste território. A proporção de formas de vida varia de acordo com os diferentes Domínios: árvores são mais expressivas na Amazônia e Floresta Atlântica do que nos outros biomas, ervas são dominantes no Pampa e as lianas apresentam riqueza expressiva na Amazônia, Floresta Atlântica e Pantanal. Este trabalho não só quantifica a biodiversidade brasileira, mas também indica as lacunas de conhecimento e o desafio a ser enfrentado para a conservação desta flora.
Abstract An updated inventory of Brazilian seed plants is presented and offers important insights into the country's biodiversity. This work started in 2010, with the publication of the Plants and Fungi Catalogue, and has been updated since by more than 430 specialists working online. Brazil is home to 32,086 native Angiosperms and 23 native Gymnosperms, showing an increase of 3% in its species richness in relation to 2010. The Amazon Rainforest is the richest Brazilian biome for Gymnosperms, while the Atlantic Rainforest is the richest one for Angiosperms. There was a considerable increment in the number of species and endemism rates for biomes, except for the Amazon that showed a decrease of 2.5% of recorded endemics. However, well over half of Brazillian seed plant species (57.4%) is endemic to this territory. The proportion of life-forms varies among different biomes: trees are more expressive in the Amazon and Atlantic Rainforest biomes while herbs predominate in the Pampa, and lianas are more expressive in the Amazon, Atlantic Rainforest, and Pantanal. This compilation serves not only to quantify Brazilian biodiversity, but also to highlight areas where there information is lacking and to provide a framework for the challenge faced in conserving Brazil's unique and diverse flora.
https://doi.org/10.1590/2175-7860201566411
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