Abstract
The combined occurrence of hereditary nephritis with nerve deafness (Alport's syndrome) and macrothrombocytopathic thrombocytopenia is very rare. The authors have had the opportunity to study such a case in a 20-year-old man who had been followed since birth. The clinical history, renal biopsy, platelet studies, and autopsy findings are presented. The renal pathologic findings are well defined; however, the hemostatic abnormalities and the hearing loss are not well characterized. In this paper, an attempt is made to clarify the diverse platelet functional and morphologic abnormalities.
Original language | English (US) |
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Pages (from-to) | 111-117 |
Number of pages | 7 |
Journal | American journal of clinical pathology |
Volume | 72 |
Issue number | 1 |
DOIs | |
State | Published - Jan 1 1979 |
ASJC Scopus subject areas
- Pathology and Forensic Medicine