Neuronal ceroid lipofuscinosis in the South American-Caribbean region: An epidemiological overview

被引:7
作者
Guelbert, Guillermo [1 ,2 ]
Venier, Ana Clara [1 ,3 ,4 ]
Cismondi, Ines Adriana [1 ,5 ]
Becerra, Adriana [1 ,2 ]
Vazquez, Juan Carlos [6 ]
Fernandez, Elmer Andres [6 ]
De Paul, Ana Lucia [3 ,4 ]
Guelbert, Norberto [1 ,7 ]
Noher, Ines [1 ,8 ]
Pesaola, Favio [1 ,9 ]
机构
[1] Hosp Ninos Santisima Trinidad, Programa Invest Translac Lipofuscinosis Ceroidea, Cordoba, Argentina
[2] Hosp Ninos Santisima Trinidad, Serv Enfermedades Metab Hereditarias, Cordoba, Argentina
[3] Univ Nacl Cordoba, Fac Ciencias Med, Ctr Microscopia Elect, Cordoba, Argentina
[4] Consejo Nacl Invest Cient & Tecn, Inst Invest Ciencias Salud, Cordoba, Argentina
[5] Univ Nacl Cordoba, Fac Odontol, Cordoba, Argentina
[6] Univ Catolica Cordoba, Ctr Invest & Desarrollo Inmunol & Enfermedades In, CONICET, Cordoba, Argentina
[7] Clin Univ Reina Fabiola, Serv Enfermedades Metab Hereditarias, Cordoba, Argentina
[8] Univ Nacl Cordoba, Cordoba, Argentina
[9] Washington Univ, Sch Med, Dept Pediat, St Louis, MO 63130 USA
关键词
neuronal ceroid lipofuscinoses (NCL); South America-Caribbean; epidemiology; genotype; phenotype; CLN8; DISEASE; VARIANT; DIAGNOSIS; MUTATIONS; PARKINSONISM; GUIDELINES; PHENOTYPE; SPECTRUM;
D O I
10.3389/fneur.2022.920421
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Neuronal ceroid lipofuscinoses (NCLs) comprise 13 hereditary neurodegenerative pathologies of very low frequency that affect individuals of all ages around the world. All NCLs share a set of symptoms that are similar to other diseases. The exhaustive collection of data from diverse sources (clinical, genetic, neurology, ophthalmology, etc.) would allow being able in the future to define this group with greater precision for a more efficient diagnostic and therapeutic approach. Despite the large amount of information worldwide, a detailed study of the characteristics of the NCLs in South America and the Caribbean region (SA&C) has not yet been done. Here, we aim to present and analyse the multidisciplinary evidence from all the SA&C with qualitative weighting and biostatistical evaluation of the casuistry. Seventy-one publications from seven countries were reviewed, and data from 261 individuals (including 44 individuals from the Cordoba cohort) were collected. Each NCL disease, as well as phenotypical and genetic data were described and discussed in the whole group. The CLN2, CLN6, and CLN3 disorders are the most frequent in the region. Eighty-seven percent of the individuals were 10 years old or less at the onset of symptoms. Seizures were the most common symptom, both at onset (51%) and throughout the disease course, followed by language (16%), motor (15%), and visual impairments (11%). Although symptoms were similar in all NCLs, some chronological differences could be observed. Sixty DNA variants were described, ranging from single nucleotide variants to large chromosomal deletions. The diagnostic odyssey was probably substantially decreased after medical education activities promoted by the pharmaceutical industry and parent organizations in some SA&C countries. There is a statistical deviation in the data probably due to the approval of the enzyme replacement therapy for CLN2 disease, which has led to a greater interest among the medical community for the early description of this pathology. As a general conclusion, it became clear in this work that the combined bibliographical/retrospective evaluation approach allowed a general overview of the multidisciplinary components and the epidemiological tendencies of NCLs in the SA&C region.
引用
收藏
页数:12
相关论文
共 53 条
[1]   Guidelines for incorporating scientific knowledge and practice on rare diseases into higher education: neuronal ceroid lipofuscinoses as a model disorder [J].
Adriana Cismondi, Ines ;
Kohan, Romina ;
Adams, Heather ;
Bond, Mike ;
Brown, Rachel ;
Cooper, Jonathan D. ;
de Hidalgo, Perla K. ;
Holthaus, Sophia-Martha Kleine ;
Mole, Sara E. ;
Mugnaini, Julia ;
Maria Oller de Ramirez, Ana ;
Pesaola, Favio ;
Rautenberg, Gisela ;
Platt, Frances M. ;
Noher de Halac, Ines .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2015, 1852 (10) :2316-2323
[2]   Retinal function in patients with the neuronal ceroid lipofuscinosis phenotype [J].
Aparecida Barasnevicius Quagliato, Elizabeth Maria ;
Rocha, Daniel Martins ;
Sacai, Paula Yuri ;
Watanabe, Sung Song ;
Salomao, Solange Rios ;
Berezovsky, Adriana .
ARQUIVOS BRASILEIROS DE OFTALMOLOGIA, 2017, 80 (04) :215-219
[3]   Neuronal Ceroid Lipofuscinosis Type 6 (CLN6) clinical findings and molecular diagnosis: Costa Rica's experience [J].
Badilla-Porras, R. ;
Echeverri-McCandless, A. ;
Weimer, J. M. ;
Ulate-Campos, A. ;
Soto-Rodriguez, A. ;
Gutierrez-Mata, A. ;
Hernandez-Con, L. ;
Bogantes-Ledezma, S. ;
Balmaceda-Meza, A. ;
Brudvig, J. ;
Sanabria-Castro, A. .
ORPHANET JOURNAL OF RARE DISEASES, 2022, 17 (01)
[4]  
Bajaj L, 2020, J CLIN INVEST, V130, P4118, DOI [10.1172/JCl130955, 10.1172/JCI130955]
[5]   Deficiency of the Lysosomal Protein CLN5 Alters Lysosomal Function and Movement [J].
Basak, Indranil ;
Hansen, Rachel A. ;
Ward, Michael E. ;
Hughes, Stephanie M. .
BIOMOLECULES, 2021, 11 (10)
[6]   CLN8 disease caused by large genomic deletions [J].
Beesley, Clare ;
Guerreiro, Rita J. ;
Bras, Jose T. ;
Williams, Ruth E. ;
Taratuto, Ana Lia ;
Eltze, Christin ;
Mole, Sara E. .
MOLECULAR GENETICS & GENOMIC MEDICINE, 2017, 5 (01) :85-91
[7]   Clinical Spectrum of Kufor-Rakeb Syndrome in the Chilean Kindred with ATP13A2 Mutations [J].
Behrens, Maria I. ;
Brueggemann, Norbert ;
Chana, Pedro ;
Venegas, Pablo ;
Kaegi, Marianne ;
Parrao, Teresa ;
Orellana, Patricia ;
Garrido, Cristian ;
Rojas, Cecilia V. ;
Hauke, Jan ;
Hahnen, Eric ;
Gonzalez, Rafael ;
Seleme, Nicolas ;
Fernandez, Veronica ;
Schmidt, Alexander ;
Binkofski, Ferdinand ;
Koempf, Detlef ;
Kubisch, Christian ;
Hagenah, Johann ;
Klein, Christine ;
Ramirez, Alfredo .
MOVEMENT DISORDERS, 2010, 25 (12) :1929-1937
[8]   Diagnosis and misdiagnosis of adult neuronal ceroid lipofuscinosis (Kufs disease) [J].
Berkovic, Samuel F. ;
Staropoli, John F. ;
Carpenter, Stirling ;
Oliver, Karen L. ;
Kmoch, Stanislav ;
Anderson, Glenn W. ;
Damiano, John A. ;
Hildebrand, Michael S. ;
Sims, Katherine B. ;
Cotman, Susan L. ;
Bahlo, Melanie ;
Smith, Katherine R. ;
Cadieux-Dion, Maxime ;
Cossette, Patrick ;
Jedlickova, Ivana ;
Pristoupilova, Anna ;
Mole, Sara E. .
NEUROLOGY, 2016, 87 (06) :579-584
[9]   CLN2/TPP1 deficiency:: The novel mutation IVS7-10A>G causes intron retention and is associated with a mild disease phenotype [J].
Bessa, C. ;
Teixeira, C. A. ;
Dias, A. ;
Alves, M. ;
Rocha, S. ;
Lacerda, L. ;
Loureiro, L. ;
Guimaraes, A. ;
Ribeiro, M. G. .
MOLECULAR GENETICS AND METABOLISM, 2008, 93 (01) :66-73
[10]   Neuronal ceroid lipofuscinosis. Type 6 late infantile variant in two compound heterozygous siblings with novel mutations [J].
Bravo Oro, Antonio ;
Saavedra Alanis, Victor M. ;
Reyes Vaca, Jorge Guillermo ;
Espinosa Tanguma, Ricardo ;
Shiguetomi Medina, Juan Manuel ;
Esmer, Carmen .
REVISTA DE NEUROLOGIA, 2021, 73 (10) :368-371