Alport syndrome: deducing the mode of inheritance from the presence of haematuria in family members
Alport syndrome: deducing the mode of inheritance from the presence of haematuria in family members
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Publisher
Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title
Language
English
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Publisher
Berlin/Heidelberg: Springer Berlin Heidelberg
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Scope and Contents
Contents
The diagnosis of Alport syndrome is suspected when an individual has haematuria or renal failure, together with a hearing loss; haematuria or renal failure, and a family history of Alport syndrome; or a pathognomonic Alport feature, such as lenticonus, fleck retinopathy, a lamellated glomerular basement membrane (GBM), or a GBM that lacks the colla...
Alternative Titles
Full title
Alport syndrome: deducing the mode of inheritance from the presence of haematuria in family members
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Author / Creator
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Record Identifier
TN_cdi_proquest_miscellaneous_2149025095
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2149025095
Other Identifiers
ISSN
0931-041X
E-ISSN
1432-198X
DOI
10.1007/s00467-018-4121-1
