Gelişmiş Arama

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dc.contributor.authorElmas, Muhsin
dc.contributor.authorGöğüş, Başak
dc.contributor.authorKılıçarslan, Furkan
dc.contributor.authorBükülmez, Ayşegül
dc.contributor.authorSolak, Mustafa
dc.date.accessioned2021-05-05T22:14:03Z
dc.date.available2021-05-05T22:14:03Z
dc.date.issued2021
dc.identifier.issn2146-4596
dc.identifier.issn2146-460X
dc.identifier.urihttps://doi.org/10.1055/s-0040-1708555
dc.identifier.urihttps://hdl.handle.net/20.500.12933/242
dc.descriptionElmas, Muhsin/0000-0002-5626-2160en_US
dc.descriptionWOS:000613901500014en_US
dc.descriptionPubMed: 33552644en_US
dc.description.abstractMucopolysaccharidosis type IIIB (Sanfilippo's B; OMIM no.: 252920) is a lysosomal storage disorder caused by defective degradation of heparan sulfate. The enzyme that has decreased function in this disease is alpha-N acetylglucosaminidase. This enzyme is encoded by the NAGLU gene. A 9-year-old male patient was referred to us with speech disability, developmental delay, hepatomegaly, mild learning disability, and otitis media with effusion complaints. Whole exome sequencing (WES) was performed because of consanguinity between the parents of the patient and the lack of specific prediagnosis. As a result of the patient's WES analysis, a homozygous mutation was detected in the NAGLU gene. The leukocyte enzyme activity was then evaluated to confirm the diagnosis. Alpha-N acetylglucosaminidase deficiency was found. Alpha-N acetylglucosaminidase activity was 0.2nmol/mLh. WES is a successful diagnostic method in the diagnosis of the mild clinical diseases with recessive inheritance. In addition, our case is a good example of genotype to phenotype diagnosis. Because in storage diseases, the diagnosis is made by leukocyte enzyme analysis first, and then the result is confirmed by gene analysis. The opposite situation occurred in our case.en_US
dc.language.isoengen_US
dc.publisherGeorg Thieme Verlag Kgen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectmucopolysaccharidosis IIIen_US
dc.subjectSanfilippo's syndrome Ben_US
dc.subjectconsanguineous marriageen_US
dc.subjectwhole exome sequencingen_US
dc.titleGenotype to Phenotype: Identification of Mucopolysaccharidosis Type IIIB (Sanfilippo's B) Case Using Whole Exome Sequencingen_US
dc.typearticleen_US
dc.departmentAFSÜ, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Tıbbi Genetik Ana Bilim Dalıen_US
dc.contributor.institutionauthorElmas, Muhsin
dc.contributor.institutionauthorGöğüş, Başak
dc.contributor.institutionauthorBükülmez, Ayşegül
dc.contributor.institutionauthorSolak, Mustafa
dc.identifier.doi10.1055/s-0040-1708555
dc.identifier.volume10en_US
dc.identifier.issue01en_US
dc.identifier.startpage74en_US
dc.identifier.endpage76en_US
dc.relation.journalJournal Of Pediatric Geneticsen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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