Practical recommendations for diagnosis, management, and follow-up of Niemann-Pick type-C disease patients: a Brazilian perspective

Niemann-Pick type-C (NPC) disease is a rare genetic condition with a clinical spectrum ranging from a fatal prenatally-presenting and quickly lethal disorder to an adult-onset chronic neurodegenerative condition. Given the scarcity of information regarding NPC disease in Brazil, a group of experts decided to discuss some disease-related aspects at the national level. The present manuscript describes the results of a Brazilian consensus meeting conducted to propose recommendations for the diagnosis, management, and follow-up of NPC disease in Brazil, considering the clinical practice point of view. These recommendations include patient characteristics on clinical presentation, as systemic and neurological manifestations according to the age group and atypical manifestations; a flowchart for diagnostic confirmation, considering the Brazilian scenario; and treatment, encompassing disease-modifying therapy, supportive care, and patients' follow-up. The expert panel provided an objective basis of recommendations on NPC diagnosis and management in Brazil. The authors expect that this manuscript will help clinicians to identify, adequately treat and follow-up NPC patients in Brazil.

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Publication Details

Journal
Arquivos de Neuro-Psiquiatria
Published
2025-03-01
DOI
https://doi.org/10.1055/s-0045-1807714
Citations
2
Primary Topic
Lysosomal Storage Disorders Research
Type
article
Field-Weighted Citation Impact
2.33

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article

Practical recommendations for diagnosis, management, and follow-up of Niemann-Pick type-C disease patients: a Brazilian perspective

Carolina Fischinger Moura de Souza, Marcondes C. França, Emília Katiane Embiruçu de Araújo Leão, Charles Marques Lourenço et al.
2 citations
Arquivos de Neuro-Psiquiatria
Lysosomal Storage Disorders Research
2.33
article

Practical recommendations for diagnosis, management, and follow-up of Niemann-Pick type-C disease patients: a Brazilian perspective

Carolina Fischinger Moura de Souza, Marcondes C. França, Emília Katiane Embiruçu de Araújo Leão, Charles Marques Lourenço, André Luiz Santos Pessoa, Dafne Dain Gandelman Horovitz, Pedro Braga‐Neto, Roberto Giugliani
article en
2 citations

Abstract

Niemann-Pick type-C (NPC) disease is a rare genetic condition with a clinical spectrum ranging from a fatal prenatally-presenting and quickly lethal disorder to an adult-onset chronic neurodegenerative condition. Given the scarcity of information regarding NPC disease in Brazil, a group of experts decided to discuss some disease-related aspects at the national level. The present manuscript describes the results of a Brazilian consensus meeting conducted to propose recommendations for the diagnosis, management, and follow-up of NPC disease in Brazil, considering the clinical practice point of view. These recommendations include patient characteristics on clinical presentation, as systemic and neurological manifestations according to the age group and atypical manifestations; a flowchart for diagnostic confirmation, considering the Brazilian scenario; and treatment, encompassing disease-modifying therapy, supportive care, and patients' follow-up. The expert panel provided an objective basis of recommendations on NPC diagnosis and management in Brazil. The authors expect that this manuscript will help clinicians to identify, adequately treat and follow-up NPC patients in Brazil.

Arquivos de Neuro-PsiquiatriaVol. 83(03)
Universidade Federal do Rio Grande do Sul (BR), Faculdade de Medicina de São José do Rio Preto (BR), Universidade Estadual de Campinas (UNICAMP) (BR), Universidade Federal do Ceará (BR), Complexo Hospitalar Universitário Professor Edgard Santos (BR), Centro Brasileiro de Estudos em Dermatologia (BR), Hospital de Clínicas de Porto Alegre (BR), Instituto Nacional de Saúde (MZ), Hospital Infantil Albert Sabin (BR), Instituto de Medicina Genómica (ES), Universidade Salvador (BR)
Cilag
Good health and well-being
Openalex Percentile: Top 13%
Lysosomal Storage Disorders Research
2.33
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