Search results for "Glycogen storage disease type IV"

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Severe neonatal onset of glycogenosis type IV: Clinical and laboratory findings leading to diagnosis in two siblings

2005

Glycogenosis type IV is an autosomal recessive disease, exceptionally diagnosed at birth: only very few reports of the fatal perinatal neuromuscular form have been described. We report on two sibling male newborns who died at 10 and 4 weeks of age with clinical signs of a systemic storage disease. Prenatal history included polyhydramnios, reduced fetal movements and fetal hydrops, and Caesarean section was performed at 36 weeks of gestational age because of fetal distress. At birth, both babies showed severe hypotonia, hyporeflexia and no spontaneous breathing activity. They never showed active movements, sucking and swallowing and were respirator-dependent until death. A muscle biopsy reve…

Central Nervous SystemMaleCytoplasmPolyhydramniosPathologymedicine.medical_specialtyGenes RecessiveAutopsyNeonatal onsetGlycogen Storage Disease Type IVFatal Outcomeneonate glycogenosis onsetGeneticsFetal distressHumansMedicineTissue DistributionAge of OnsetMuscle SkeletalGenetics (clinical)Family HealthMuscle biopsymedicine.diagnostic_testbusiness.industryInfant NewbornInfantHyporeflexiamedicine.diseaseHypotoniaFetal movementAutopsymedicine.symptombusinessGlycogenJournal of Inherited Metabolic Disease
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A mild juvenile variant of type IV glycogenosis.

1992

The mild juvenile form of type IV glycogenosis, confirmed by a profound deficiency of the brancher enzyme in tissue specimens is reported from three Turkish male siblings who, foremost, suffered from chronic progressive myopathy. Muscle fibers contained polyglucosan inclusions of typical fine structure, i.e. a mixture of granular and filamentous glycogen. They reacted strongly for myophosphorylase, but were resistant to diastase. These inclusions were ubiquitinated and reacted with antibody KM-279 which previously has been shown to bind to Lafora bodies, corpora amylacea and polyglucosan material in hepatic and cardiac cells of type IV glycogenosis as well as polyglucosan body myopathy with…

Muscle tissueMalemedicine.medical_specialtyBiologychemistry.chemical_compoundGlycogen Storage Disease Type IVDevelopmental NeuroscienceInternal medicineSweat glandmedicineHumansGlycogen storage disease type IVMyopathyChildGlycogenStaining and LabelingHistocytochemistryMusclesInfantGeneral Medicinemedicine.diseaseEnzyme assaySweat Glandsmedicine.anatomical_structureEndocrinologychemistryMyophosphorylasePediatrics Perinatology and Child Healthbiology.proteinNeurology (clinical)medicine.symptomCorpora amylaceaBraindevelopment
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Branching enzyme deficiency/glycogenosis storage disease type IV presenting as a severe congenital hypotonia: muscle biopsy and autopsy findings, bio…

2010

The fatal infantile neuromuscular presentation of branching enzyme deficiency (glycogen storage disease type IV) due to mutations in the gene encoding the glycogen branching enzyme, is a rare but probably underdiagnosed cause of congenital hypotonia. We report an infant girl with severe generalized hypotonia, born at 33 weeks gestation who required ventilatory assistance since birth. She had bilateral ptosis, mild knee and foot contractures and echocardiographic evidence of cardiomyopathy. A muscle biopsy at 1 month of age showed typical polyglucosan storage. The autopsy at 3.5 months of age showed frontal cortex polymicrogyria and polyglucosan bodies in neurons of basal ganglia, thalamus, …

Pathologymedicine.medical_specialtyMuscle HypotoniaCardiomyopathyAutopsyGlycogen Storage Disease Type IVFatal Outcome14-alpha-Glucan Branching EnzymemedicineGlycogen branching enzymePolymicrogyriaHumansGlycogen storage disease type IVMuscle SkeletalGenetics (clinical)Muscle biopsymedicine.diagnostic_testbiologyInfant NewbornBrainInfantmedicine.diseaseNeurologyPediatrics Perinatology and Child Healthbiology.proteinMuscle HypotoniaFemaleNeurology (clinical)Differential diagnosisInfant PrematureNeuromuscular disorders : NMD
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