Reinfection of COVID‐19 after 3 months with a distinct and more aggressive clinical presentation: Case report von Torres, Danielle de Araujo, Ribeiro, Luciana do Carmo Bueno, Riello, Anna Patrícia de Freitas Linhares, Horovitz, Dafne Dain Gandelman, Pinto, Luis Felipe Ribeiro, Croda, Julio

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Laryngeal, Tracheal, and Bronchial Disease in the Mucopolysaccharidoses: Endoscopic Study von Pires de Mello, Paulo, Lopes Barth, Anneliese, de Araujo Torres, Danielle, Pires de Mello Valente, Mariana, Dain Gandelman Horovitz, Dafne

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Cranial bone collapse in microcephalic infants prenatally exposed to Zika virus infection von Dain Gandelman Horovitz, Dafne, da Silva Pone, Marcos Vinicius, Moura Pone, Sheila, Dias Saad Salles, Tania Regina, Bastos Boechat, Marcia Cristina

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Identification of relevant International Classification of Functioning Disability and Health (ICF) categories in patients with 22q11.2 Deletion Syndrome: a Delphi exercise von Corrêa, Ana Paula Carvalho, Ribeiro, Carla Trevisan Martins, Horovitz, Dafne Dain Gandelman, Ribeiro, Luciana Castaneda

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Alternative laronidase dose regimen for patients with mucopolysaccharidosis I: a multinational, retrospective, chart review case series von Horovitz, Dafne Dain Gandelman, Acosta, Angelina X, Giugliani, Roberto, Hlavatá, Anna, Hlavatá, Katarína, Tchan, Michel C, Lopes Barth, Anneliese, Cardoso, Jr, Laercio, Embiruçu de Araújo Leão, Emília Katiane, Esposito, Ana Carolina, Kyosen, Sandra Obikawa, De Souza, Carolina Fischinger Moura, Martins, Ana Maria

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Genetics and genomics in Brazil: a promising future von Passos‐Bueno, Maria Rita, Bertola, Debora, Horovitz, Dafne Dain Gandelman, Faria Ferraz, Victor Evangelista, Brito, Luciano Abreu

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Identification of a founder effect involving n.197C>T variant in RMRP gene associated to cartilage-hair hypoplasia syndrome in Brazilian patients von Gomes, Maria Eduarda, Kehdy, Fernanda, de Neves-Manta, Fernanda Saloum, Horovitz, Dafne Dain Gandelman, Sanseverino, Maria Teresa, Leal, Gabriela Ferraz, Felix, Têmis Maria, Cavalcanti, Denise Pontes, Llerena, Juan Clinton, Gonzalez, Sayonara

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Medical Genetics in Brazil in the 21st Century: A Thriving Specialty and Its Incorporation in Public Health Policies von Horovitz, Dafne Dain Gandelman, Félix, Têmis Maria, Ferraz, Victor Evangelista de Faria

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Enzyme replacement therapy for Mucopolysaccharidosis Type I among patients followed within the MPS Brazil Network von Dornelles, Alícia Dorneles, de Camargo Pinto, Louise Lapagesse, de Paula, Ana Carolina, Steiner, Carlos Eduardo, Lourenço, Charles Marques, Kim, Chong Ae, Horovitz, Dafne Dain Gandelman, Ribeiro, Erlane Marques, Valadares, Eugênia Ribeiro, Goulart, Isabela, Neves de Souza, Isabel C, da Costa Neri, João Ivanildo, Santana-da-Silva, Luiz Carlos, Silva, Luiz Roberto, Ribeiro, Márcia, de Oliveira Sobrinho, Ruy Pires, Giugliani, Roberto, Schwartz, Ida Vanessa Doederlein

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Genetic services and testing in Brazil von Horovitz, Dafne Dain Gandelman, de Faria Ferraz, Victor Evangelista, Dain, Sulamis, Marques-de-Faria, Antonia Paula

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Mucopolysaccharidosis VII in Brazil: natural history and clinical findings von Giugliani, Roberto, Barth, Anneliese Lopes, Dumas, Melissa Rossi Calvão, da Silva Franco, José Francisco, de Rosso Giuliani, Liane, Grangeiro, Carlos Henrique Paiva, Horovitz, Dafne Dain Gandelman, Kim, Chong Ae, de Araújo Leão, Emilia Katiane Embiruçu, de Medeiros, Paula Frassinetti Vasconcelos, Miguel, Diego Santana Chaves Geraldo, Moreira, Maria Espírito Santo Almeida, dos Santos, Helena Maria Guimarães Pimentel, da Silva, Luiz Carlos Santana, da Silva, Luiz Roberto, de Souza, Isabel Neves, Nalin, Tatiele, Garcia, Daniel

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Complex care, high cost, and loss of income: frequent issues for families of children and adolescents with rare health conditions von Pinto, Márcia, Madureira, Adelino, Barros, Letícia Baptista de Paula, Nascimento, Marcos, Costa, Ana Carolina Carioca da, Oliveira, Nicole Velloso de, Albernaz, Lidianne, Campos, Daniel de Souza, Horovitz, Dafne Dain Gandelman, Martins, Antilia Januária, Moreira, Martha Cristina Nunes

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When rarity is an asset: political activism for the rights of persons with rare diseases in the Brazilian Unified National Health System von Moreira, Martha Cristina Nunes, Nascimento, Marcos Antonio Ferreira do, Horovitz, Dafne Dain Gandelman, Martins, Antilia Januaria, Pinto, Marcia

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Treatment networks and associations of patients with rare diseases von Lima, Maria Angelica de Faria Domingues de, Gilbert, Ana Cristina Bohrer, Horovitz, Dafne Dain Gandelman

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The 22q11.2 Deletion Syndrome from A Biopsychosocial Perspective: A Series of Cases with an ICF-Based Approach von Cabral, Ana Paula Corrêa, Horovitz, Dafne Dain Gandelman, Santos, Lidiane Nogueira, Carvalho, Amanda Oliveira de, Wigg, Cristina Maria Duarte, Castaneda, Luciana, Simon, Liane, Ribeiro, Carla Trevisan Martins

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Neurological Phenotypes of IRF2BPL Gene Variants: A Report of Four Novel Variants von Horovitz, Dafne Dain Gandelman, de Faria Domingues de Lima, Maria Angelica, Pires, Lais de Carvalho, Campos Araujo, Abelardo de Queiroz, Vargas, Fernando Regla

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Enzyme replacement therapy interruption in mucopolysaccharidosis type IVA patients and its impact in different clinical outcomes von Politei, Juan, Porras‐Hurtado, Gloria Liliana, Guelbert, Norberto, Fainboim, Alejandro, Horovitz, Dafne Dain Gandelman, Satizábal, José María

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Rare diseases and the associative dialogue: resignifications for moral experiences von Moreira, Martha Cristina Nunes, Nascimento, Marcos Antonio Ferreira do, Campos, Daniel de Souza, Albernaz, Lidianne, Costa, Ana Carolina Carioca da, Barros, Letícia Baptista de Paula, Horovitz, Dafne Dain Gandelman, Martins, Antilia Januária, Madureira, Adelino Furtado, Oliveira, Nicole Velloso de, Pinto, Márcia

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Intrathecal administration of recombinant human N-acetylgalactosamine 4-sulfatase to a MPS VI patient with pachymeningitis cervicalis von Muñoz-Rojas, María Verónica, Horovitz, Dafne Dain Gandelman, Jardim, Laura Bannach, Raymundo, Marcia, Llerena, Juan Clinton, de Magalhães, Tatiana de Sá Carneiro Pacheco, Vieira, Taiane Alves, Costa, Ronaldo, Kakkis, Emil, Giugliani, Roberto

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Oral and craniofacial manifestations in a Hunter syndrome patient with hematopoietic stem cell transplantation: A case report von Torres, Rafaela de Oliveira, Pintor, Andréa Vaz Braga, Guedes, Fábio Ribeiro, Freitas‐Fernandes, Liana Bastos, Barth, Anneliese Lopes, Horovitz, Dafne Dain Gandelman, Souza, Ivete Pomarico Ribeiro

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