Search results for "CDG"

showing 8 items of 8 documents

Are the new genetic tools for diagnosis of Wilson disease helpful in clinical practice?

2020

Summary The diagnosis of Wilson disease is not always easy. For many patients, a combination of tests reflecting disturbed copper metabolism may be needed. Testing for ATP7B variants has become part of the routine diagnostic approach. The methods of genetic testing include analysis of the 21 coding exons and intronic flanking sequences, in which exons with recurrent variants would be prioritised depending on the mutation frequency in the local population. If sequencing the entire ATP7B gene cannot identify 2 variants and the suspicion for Wilson disease is high, after reviewing the clinical data, WES (whole-exome sequencing) or WGS (whole-genome sequencing) could be applied. A workflow base…

DiseaseReviewIndian childhood cirrhosisBioinformaticsDNA sequencingWES whole-exome sequencingPFIC progressive familial intrahepatic cholestasisInternal MedicinemedicineImmunology and AllergyMultiplex ligation-dependent probe amplificationWGS whole-genome sequencingExome sequencingGenetic testingWilson diseaseWhole genome sequencingWhole-genome sequencingHepatologymedicine.diagnostic_testMEDNIK syndromebusiness.industryCopper metabolismGastroenterologyMLPA multiplex ligation-dependent probe amplificationmedicine.diseaseICC Indian childhood cirrhosisNGS next-generation sequencingDMR differentially methylated regionsWhole-exome sequencingNext-generation sequencingbusinessICT idiopathic or primary copper toxicosisCDG congenital disorders of glycosylationGenetic diseasesJHEP Reports
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Heterodimerization of Two Pathological Mutants Enhances the Activity of Human Phosphomannomutase2

2015

The most frequent disorder of glycosylation is due to mutations in the gene encoding phosphomannomutase2 (PMM2-CDG). For this disease, which is autosomal and recessive, there is no cure at present. Most patients are composite heterozygous and carry one allele encoding an inactive mutant, R141H, and one encoding a hypomorphic mutant. Phosphomannomutase2 is a dimer. We reproduced composite heterozygosity in vitro by mixing R141H either with the wild type protein or the most common hypomorphic mutant F119L and compared the quaternary structure, the activity and the stability of the heterodimeric enzymes. We demonstrated that the activity of R141H/F119L heterodimers in vitro, which reproduces t…

Genetics and Molecular Biology (all)HeterozygoteProtein StructureGlycosylationMutantlcsh:MedicineGlucose-6-PhosphateBiologymedicine.disease_causeBiochemistryQuaternaryCongenital Disorders of GlycosylationProtein structuremedicineAlleles; Congenital Disorders of Glycosylation; Dimerization; Glucose-6-Phosphate; Glycosylation; Heterozygote; Humans; Mutation; Phosphorylation; Phosphotransferases (Phosphomutases); Protein Structure Quaternary; Agricultural and Biological Sciences (all); Biochemistry Genetics and Molecular Biology (all); Medicine (all)HumansPhosphorylationAlleleProtein Structure Quaternarylcsh:ScienceGeneAllelesMutationMultidisciplinaryMedicine (all)lcsh:RWild typeMolecular biologyEnzyme structureProteostasisAgricultural and Biological Sciences (all)heterodimresPhosphotransferases (Phosphomutases)Mutationlcsh:QCDG-PMM2DimerizationResearch ArticlePLOS ONE
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An Unexplained Congenital Disorder of Glycosylation-II in a Child with Neurohepatic Involvement, Hypercholesterolemia and Hypoceruloplasminemia

2017

We report on a 12-year-old adopted boy with psychomotor disability, absence seizures, and normal brain MRI. He showed increased (but initially, at 5 months, normal) serum cholesterol, increased alkaline phosphatases, transiently increased transaminases and hypoceruloplasminemia with normal serum and urinary copper. Blood levels of immunoglobulins, haptoglobin, antithrombin, and factor XI were normal. A type 2 serum transferrin isoelectrofocusing and hypoglycosylation of apoCIII pointed to a combined N- and O-glycosylation defect. Neither CDG panel analysis with 79 CDG-related genes, nor whole exome sequencing revealed the cause of this CDG. Whole genome sequencing was not performed since th…

Hypoceruloplasminemiacongenital hereditary and neonatal diseases and abnormalitiesmedicine.medical_specialtySettore MED/09 - Medicina InternaUrinary systemHypercholesterolemiaArticleInternal medicineNeurohepatic involvementmedicineCDG-IIGlycomicsExome sequencingWhole genome sequencingchemistry.chemical_classificationbiologybusiness.industryHaptoglobinAntithrombinmedicine.diseaseDisorders of movement Donders Center for Medical Neuroscience [Radboudumc 3]EndocrinologyMALDI TOFchemistryTransferrinbiology.proteinCDGAntibodybusinessCongenital disorder of glycosylationmedicine.drug
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Key features and clinical variability of COG6-CDG

2015

The conserved oligomeric Golgi (COG) complex consists of eight subunits and plays a crucial role in Golgi trafficking and positioning of glycosylation enzymes. Mutations in all COG subunits, except subunit 3, have been detected in patients with congenital disorders of glycosylation (CDG) of variable severity. So far, 3 families with a total of 10 individuals with biallelic COG6 mutations have been described, showing a broad clinical spectrum. Here we present 7 additional patients with 4 novel COG6 mutations. In spite of clinical variability, we delineate the core features of COG6-CDG i.e. liver involvement (9/10), microcephaly (8/10), developmental disability (8/10), recurrent infections (7…

MaleMicrocephalyGlycosylationAdolescentEndocrinology Diabetes and MetabolismProtein subunitHyperkeratosisMolecular Sequence DataGolgi ApparatusCase ReportsResearch SupportBiochemistryConserved oligomeric Golgi complexYoung AdultEndocrinologyCogCongenital Disorders of GlycosylationGeneticsJournal ArticleMedicineHumansNon-U.S. Gov'tChildMolecular BiologyExome sequencingGenetic Association StudiesGeneticsbusiness.industryConserved oligomeric Golgi complexResearch Support Non-U.S. Gov'tHigh-Throughput Nucleotide SequencingInfantCongenital disorder of glycosylationmedicine.diseasePhenotypeAdaptor Proteins Vesicular TransportPhenotypeCOG6MutationMicrocephalyFemaleCDGbusinessCongenital disorder of glycosylation
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Sindrome CDG tipo I: un caso ad elevata espressività clinica

2009

Settore MED/38 - Pediatria Generale E Specialisticasindromi CDG isoelettrofocusing delle transferrine
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Suomen CDG-mallia kehittämässä : oppilaiden kokemukset oppijakeskeisestä liikunnanopetusinterventiosta

2015

Tässä tutkimuksessa tarkoituksenamme oli selvittää, eroavatko oppilaslähtöiseen liikunnanopetusinterventioon osallistuneiden alakoulun oppilaiden kokemukset koetusta autonomiasta, sekä liikuntaa opettavan luokanopettajan demokraattisesta käyttäytymisestä ja opettajan tarjoamasta sosiaalisesta tuesta, kontrollikoulun oppilaiden kokemuksiin verrattuna. Halusimme myös selvittää, erosivatko interventioon osallistuneiden tyttöjen ja poikien kokemukset toisistaan. Tutkimusaineisto koostui Liikuntatunnit kaikille aktiiviseksi - CDG-malli opetuksen tukena - hankkeesta, joka toteutettiin marraskuun 2011 ja maaliskuun 2013 välisenä aikana. Interventio pohjautui australialaiseen Quayn ja Petersin (200…

oppilaslähtöisyysSuomen CDG-mallikoululiikuntaliikuntaopetusliikunnanopetusoppilaat
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Suomen CDG-malli : oppilaiden kokemukset oppijakeskeisestä liikunnanopetusinterventiosta

2015

Tässä tutkimuksessa tarkoituksenamme oli selvittää, eroavatko oppilaslähtöiseen liikunnanopetusinterventioon osallistuneiden alakoululaisten kokemukset koetusta autonomiasta sekä liikuntaa opettavan luokanopettajan demokraattisesta käyttäytymisestä ja hänen tarjoamastaan sosiaalisesta tuesta verrattuna kontrollikoulun oppilaiden kokemuksiin. Halusimme myös selvittää, erosivatko interventioon osallistuneiden tyttöjen ja poikien kokemukset toisistaan. Tutkimuksemme oli Jyväskylän yliopiston opettajankoulutuslaitoksen ja liikuntakasvatuksen laitoksen yhteistyönä toteuttaman Liikuntatunnit kaikille aktiiviseksi – CDG-malli opetuksen tukena -hankkeen osatutkimus, joka toteutettiin marraskuun 201…

oppilaslähtöisyysSuomen CDG-mallistudent-centered teachingkoululiikuntaschool physical educationliikunnanopetusFinnish CDG model
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Tapaustutkimus Suomen CDG- mallin kehittämisestä

2012

suunnitteluluovuusluokanopettajatCDG-malliopetusKvalitatiivinen tutkimusyhteistyöasiantuntijuuskollegiaalinen yhteistyö
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