Introduction: With its unprecedented throughput, scalability and speed, next-generation sequencing (NGS) is revolutionizing clinical research. Targeted sequencing in particular is now available in many labs. Still, whenever a novel variant is detected, its pathogenicity must be carefully assessed and every now and again, a case pops up to highlight how tricky and delicate this process can be. Here we present a case of a molecular diagnosis of a patient with a clinical suspicion of MPS type VI, where even though the causal mutation was easy to detect by both Sanger and NGS, only through indirect studies could we present proof of principle on its pathogenicity.This work was partially supported by Fundação Millennium bcp and N2020 (bcp/LIM/D...
Mucopolysaccharidosis type VI (MPS VI), or Maroteaux-Lamy syndrome, is a lysosomal storage disorder ...
Mucopolysaccharidosis type IIIC (MPSIIIC) is a severe, rare autosomal recessive disorder caused by v...
IGMJM, Unidade de Enzimologia- Porto and IBMC, Unilipe- Universidade do PortoResumo disponível em: J...
Introduction: With its unprecedented throughput, scalability and speed, next-generation sequencing (...
Here, we present the molecular diagnosis of a patient with a general clinical suspicion of Mucopolys...
Mucopolysaccharidoses (MPS) are a subgroup of 11 monogenic lysosomal storage disorders due to the de...
Mucopolysaccharidosis (MPS) are a group of rare genetic disorders caused by deficiency in the activi...
Q483-89Introduction: Maroteaux–Lamy syndrome, or mucopolysaccharidosis (MPS) type VI, is an autosoma...
Copyright © 2006 Elsevier Inc. All rights reserved.Mucopolysaccharidosis type VI (MPS VI; Maroteaux-...
Mucolipidosis II and III alpha/beta (ML II/III alpha/beta) are rare autosomal recessive lysosomal st...
In this study we have investigated a group of 29 Brazilian patients, who had been diagnosed with the...
While being well known that the diagnosis of many genetic disorders relies on a combination of clini...
Mucopolysaccharidosis type VI (MPS VI) or Maroteaux-Lamy syndrome is produced by the deficiency of t...
Mucopolysaccharidosis type VI (MPS VI; Maroteaux-Lamy syndrome) is a lysosomal storage disorder caus...
Mucopolysaccharidosis type VI (MPS VI - Maroteaux-Lamy syndrome) is a globally rare lysosomal storag...
Mucopolysaccharidosis type VI (MPS VI), or Maroteaux-Lamy syndrome, is a lysosomal storage disorder ...
Mucopolysaccharidosis type IIIC (MPSIIIC) is a severe, rare autosomal recessive disorder caused by v...
IGMJM, Unidade de Enzimologia- Porto and IBMC, Unilipe- Universidade do PortoResumo disponível em: J...
Introduction: With its unprecedented throughput, scalability and speed, next-generation sequencing (...
Here, we present the molecular diagnosis of a patient with a general clinical suspicion of Mucopolys...
Mucopolysaccharidoses (MPS) are a subgroup of 11 monogenic lysosomal storage disorders due to the de...
Mucopolysaccharidosis (MPS) are a group of rare genetic disorders caused by deficiency in the activi...
Q483-89Introduction: Maroteaux–Lamy syndrome, or mucopolysaccharidosis (MPS) type VI, is an autosoma...
Copyright © 2006 Elsevier Inc. All rights reserved.Mucopolysaccharidosis type VI (MPS VI; Maroteaux-...
Mucolipidosis II and III alpha/beta (ML II/III alpha/beta) are rare autosomal recessive lysosomal st...
In this study we have investigated a group of 29 Brazilian patients, who had been diagnosed with the...
While being well known that the diagnosis of many genetic disorders relies on a combination of clini...
Mucopolysaccharidosis type VI (MPS VI) or Maroteaux-Lamy syndrome is produced by the deficiency of t...
Mucopolysaccharidosis type VI (MPS VI; Maroteaux-Lamy syndrome) is a lysosomal storage disorder caus...
Mucopolysaccharidosis type VI (MPS VI - Maroteaux-Lamy syndrome) is a globally rare lysosomal storag...
Mucopolysaccharidosis type VI (MPS VI), or Maroteaux-Lamy syndrome, is a lysosomal storage disorder ...
Mucopolysaccharidosis type IIIC (MPSIIIC) is a severe, rare autosomal recessive disorder caused by v...
IGMJM, Unidade de Enzimologia- Porto and IBMC, Unilipe- Universidade do PortoResumo disponível em: J...