Coinheritance of novel mutations in NAGLU causing mucopolysaccharidosis type IIIB and in DDHD2 causing spastic paraplegia54 in a Turkish family

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dc.contributor.authorGun Bilgic D.
dc.contributor.authorGerik Celebi H.B.
dc.contributor.authorAydin Gumus A.
dc.contributor.authorBilgic A.
dc.contributor.authorYazici H.
dc.contributor.authorCeylaner S.
dc.contributor.authorYilmaz C.
dc.contributor.authorPolat M.
dc.contributor.authorAkbal Sahin M.
dc.contributor.authorDereli F.
dc.contributor.authorCam F.S.
dc.date.accessioned2025-04-10T11:06:14Z
dc.date.available2025-04-10T11:06:14Z
dc.date.issued2020
dc.description.abstractMucopolysaccharidosis type IIIB (MPSIIIB) is one of the lysosomal storage diseases, clinically related to developmental delay in the early phase and loss of skills in the late phases of the disease. The disease is caused by homozygous mutations in the NAGLU gene. Spastic paraplegia54 (SPG54) is a neurodegenerative disorder caused by homozygous mutations in the DDHD2 gene. Clinical features are progressive spasticity and weakness in the lower limbs and corpus callosum agenesis. We report on two siblings in a consanguineous family, presenting both the clinical and molecular diagnoses of MPSIIIB and SPG54 with novel mutations by using whole exome sequencing (WES). This interesting finding shows that we should be aware of the importance of using WES for diagnosing rare diseases in consanguineous families. © 2020 Elsevier Ltd
dc.identifier.DOI-ID10.1016/j.jocn.2020.11.007
dc.identifier.urihttp://hdl.handle.net/20.500.14701/46585
dc.publisherChurchill Livingstone
dc.titleCoinheritance of novel mutations in NAGLU causing mucopolysaccharidosis type IIIB and in DDHD2 causing spastic paraplegia54 in a Turkish family
dc.typeArticle

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