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خرید پکیج
تعداد آیتم قابل مشاهده باقیمانده : 3 مورد
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Summary of Class 1 and Class 2 defects for the ultrastructural diagnosis of PCD

Summary of Class 1 and Class 2 defects for the ultrastructural diagnosis of PCD
Class 1 defects: Hallmark diagnostic defects
ODA defect
ODA and IDA defect
Microtubular disorganisation and IDA defect
Class 2 defects: Indicate a PCD diagnosis with other supporting evidence
Central complex defect
Mislocalisation of basal bodies with few or no cilia
Microtubular disorganisation with IDA present
ODA absence from 25 to 50% of cross sections
Combined IDA and ODA absence from 25 to 50% of cross sections
Class 1 defects are diagnostic of PCD in a patient with clinical symptoms of PCD. Class 2 defects can indicate a diagnosis of PCD in a patient with clinical symptoms of the condition, if consistent across more than one sample and if consistent with other results (such as those from immunofluorescence, high speed video microscopy, or genetic analysis). Class 2 defects may require assessment of more ciliary axonemes than Class 1 defects. Care should be taken to assess cross sections from several cells and both proximal (in the region of the microvilli) and distal regions of the axoneme.
PCD: primary ciliary dyskinesia; ODA: outer dynein arm; IDA: inner dynein arm.
Reproduced with permission of the © ERS 2020: European Respiratory Journal 55 (4) 1900725. DOI: 10.1183/13993003.00725-2019. Published 16 April 2020.
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