Proteinuria in haemoglobin H disease
Joint Authors
Ratnakar, K. S.
al-Arid, Samir M.
Rajagopalan, S.
Source
Issue
Vol. 23, Issue 2 (30 Jun. 2001), pp.1-5, 5 p.
Publisher
King Hamad University Hospital
Publication Date
2001-06-30
Country of Publication
Bahrain
No. of Pages
5
Main Subjects
Abstract EN
While extensive studies are available on the renal manifestations in sickle cell disease, there is no documented evidence in favour of renal changes in the commonly encountered haemoglobinopathy namely, α thalassaemia.
A light, immuno-flourescence and electron microscopic observations on a renal biopsy of a young male patient who is a known case of Hemoglobin H disease with proteinuria is documented.
This is probably the first case reported, primarily for renal complications with demonstrable podocyte abnormalities.
The pathogenesis of renal manifestations remains obscure.
The renal alterations are less likely to be due to minimal change disease in view of immunoglobulin deposits in the mesangial area.
However involvement of any other immune process or continued sub- clinical haemolysis producing proteinuria remain to be seen on long-term studies.
American Psychological Association (APA)
Rajagopalan, S.& al-Arid, Samir M.& Ratnakar, K. S.. 2001. Proteinuria in haemoglobin H disease. Bahrain Medical Bulletin،Vol. 23, no. 2, pp.1-5.
https://search.emarefa.net/detail/BIM-602121
Modern Language Association (MLA)
Rajagopalan, S.…[et al.]. Proteinuria in haemoglobin H disease. Bahrain Medical Bulletin Vol. 23, no. 2 (Jun. 2001), pp.1-5.
https://search.emarefa.net/detail/BIM-602121
American Medical Association (AMA)
Rajagopalan, S.& al-Arid, Samir M.& Ratnakar, K. S.. Proteinuria in haemoglobin H disease. Bahrain Medical Bulletin. 2001. Vol. 23, no. 2, pp.1-5.
https://search.emarefa.net/detail/BIM-602121
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references : p. 4-5
Record ID
BIM-602121