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...
- 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/
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 |
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