| Alport's syndrome--a case report. | |
| | |
MedLine Citation:
|
PMID: 8972154 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
|
Alport's syndrome (hereditary nephritis with deafness), is an uncommon disease and is seen very infrequently in India. We report a fatal case in a young girl with characteristic ultrastructural changes in the kidney thus emphasising the exception noted in the observation that females have a better prognosis compared to males. |
| | |
Authors:
|
R A Prasad; R K Bhatnagar; C Ratnakar; A J Veliath |
Related Documents
:
|
1959544 - Desbuquois syndrome. 4009704 - The marden-walker syndrome: a case report and review of the literature. 23480044 - Replantation of avulsed primary incisors: a critical review of a controversial treatment. 21814324 - Testicular leiomyosarcoma with metastasis. 18679534 - Complications of and controversies associated with percutaneous endoscopic gastrostomy:... 22767994 - Knowledge of adverse drug reaction reporting in first year postgraduate doctors in a me... |
Publication Detail:
|
Type: Case Reports; Journal Article |
Journal Detail:
|
Title: Indian journal of pathology & microbiology Volume: 39 ISSN: 0377-4929 ISO Abbreviation: Indian J Pathol Microbiol Publication Date: 1996 Jul |
Date Detail:
|
Created Date: 1997-02-06 Completed Date: 1997-02-06 Revised Date: 2004-11-17 |
Medline Journal Info:
|
Nlm Unique ID: 7605904 Medline TA: Indian J Pathol Microbiol Country: INDIA |
Other Details:
|
Languages: eng Pagination: 225-7 Citation Subset: IM |
Affiliation:
|
Department of Pathology, JIPMER, Pondicherry. |
Export Citation:
|
APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
|
Adolescent Fatal Outcome Female Humans Kidney / ultrastructure Nephritis, Hereditary / pathology*, therapy |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
Previous Document: Congenital sulfhemoglobin and transient methemoglobinemia secondary to diarrhoea.
Next Document: Blastopathies--symmetrical conjoined twins.