| Autor: |
Fussiger, Helena, Pereira, Bruna Letícia da Silva, Padilha, Janice Pacheco Dias, Donis, Karina Carvalho, Siebert, Marina, Brusius‐Facchin, Ana Carolina, Baldo, Guilherme, Saute, Jonas Alex Morales |
| Předmět: |
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| Zdroj: |
Clinical Genetics; May2023, Vol. 103 Issue 5, p580-584, 5p |
| Abstrakt: |
Copy number variations (CNV) may represent a significant proportion of SPG4 and SPG3A diagnosis, the most frequent autosomal dominant subtypes of hereditary spastic paraplegias (HSP). We aimed to assess the frequency of CNVs in SPAST and ATL1 and to update the molecular epidemiology of HSP families in southern Brazil. A cohort study that included 95 Brazilian index cases with clinical suspicion of HSP was conducted between April 2011 and September 2022. Multiplex Ligation Dependent Probe Amplification (MLPA) was performed in 41 cases without defined diagnosis by different massive parallel sequencing techniques (MPS). Diagnosis was obtained in 57/95 (60%) index cases, 15/57 (26.3%) being SPG4. Most frequent autosomal recessive HSP subtypes were SPG7 followed by SPG11, SPG76 and cerebrotendinous xanthomatosis. No CNVs in SPAST and ATL1 were found. Copy number variations are rare among SPG4 and SPG3A families in Brazil. Considering the possibility of CNVs detection by specific algorithms with MPS data, we consider that this is likely the most cost‐effective approach to investigate CNVs in these genes in low‐risk populations, with MLPA being reserved as an orthogonal confirmatory test. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
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