Search results for "Molecular genetic classification"

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The neuronal ceroid-lipofuscinoses: A historical introduction

2013

AbstractThe neuronal ceroid-lipofuscinoses (Batten disease) collectively constitute one of the most common groups of inherited childhood onset neurodegenerative disorders, and have also been identified in many domestic and laboratory animals. The group of human neuronal ceroid-lipofuscinoses currently comprises 14 genetically distinct disorders, mostly characterised by progressive mental, motor and visual deterioration with onset in childhood or adolescence. Abnormal autofluorescent, electron-dense granules accumulate in the cytoplasm of nerve cells, and this storage process is associated with selective destruction and loss of neurons in the brain and retina. The present paper outlines near…

Batten diseaseHistoryBatten diseaseDiseaseBiology03 medical and health sciences0302 clinical medicineNeuronal Ceroid-LipofuscinosesmedicineHumansNeurodegenerationMolecular Biology030304 developmental biologyNeuronal Ceroid-Lipofuscinoses0303 health sciencesRetinaNeurodegenerationHistory 19th CenturyHistory 20th Centurymedicine.disease3. Good healthAgeingmedicine.anatomical_structureNerve cellsNeuronal ceroid-lipofuscinosisMolecular genetic classificationMolecular MedicineNeuronal ceroid lipofuscinosisIdentification (biology)Neuroscience030217 neurology & neurosurgeryBiochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
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