Síndrome de Morquio: nueva mutación del gen GALNS en dos hermanos del sur-occidente colombiano. Análisis clínico, molecular y bioinformático

Mucopolysaccharidosis type IV A, or Morquio syndrome, is an autosomal recessive lysosomal storage disorder that is caused by mutations on the GALNS gene, resulting in the accumulation of keratan sulfate and condroitin sulfate in certain tissues. It is expressed as generalized skeletal dysplasia incl...

Full description

Autores:
Pachajoa Londoño, Harry Mauricio
Castillo, Andrés
Eichler, Sabrina
Hernández Amariz, María Fernanda
Ruíz Botero, Felipe
Tipo de recurso:
Article of investigation
Fecha de publicación:
2016
Institución:
Universidad ICESI
Repositorio:
Repositorio ICESI
Idioma:
spa
OAI Identifier:
oai:repository.icesi.edu.co:10906/81413
Acceso en línea:
https://nebulosa.icesi.edu.co:2615/record/display.uri?eid=2-s2.0-84991772092&origin=resultslist&sort=plf-f&src=s&st1=S%c3%adndrome+de+Morquio&st2=S%c3%adndrome+de+Morquio&sid=E01D21DDECC54497C1F7194D30930AB0.wsnAw8kcdt7IPYLO0V48gA%3a1470&sot=b&sdt=b&sl=75&s=%28TITLE-ABS-KEY%28S%c3%adndrome+de+Morquio%29+AND+TITLE-ABS-KEY%28S%c3%adndrome+de+Morquio%29%29&relpos=0&citeCnt=0&searchTerm=
http://new.medigraphic.com/cgi-bin/resumen.cgi?IDARTICULO=67772
http://hdl.handle.net/10906/81413
Palabra clave:
Ciencias socio biomédicas
Medical sciences
Síndrome de Morquio
Bioinformática
Mucopolisacaridosis
Rights
openAccess
License
https://creativecommons.org/licenses/by-nc-nd/4.0/
Description
Summary:Mucopolysaccharidosis type IV A, or Morquio syndrome, is an autosomal recessive lysosomal storage disorder that is caused by mutations on the GALNS gene, resulting in the accumulation of keratan sulfate and condroitin sulfate in certain tissues. It is expressed as generalized skeletal dysplasia including short stature, Pectus carinatum, platyspondylia, odontoid hypoplasia, kyphoscoliosis, and genu valgum. Material and methods: 9 and 6 six year old brothers with clinical characteristic of severe Morquio syndrome. GALNS gene sequencing is performed detecting two mutations in both brothers, the fi rst one in exon 3 (c.280C>T p.R94C), and a new mutation in exon 9 (c.998G>A p.G333D), which was determined as potentially pathological. Bioinformatic analysis of the mutations via an in silico analysis of multiple sequence homology, using the Softwares SIFT, PolyPhen, nsSNPAnalyzer, I-Mutant, FOLD X, and DeepView-Swiss-PdbView