-transparent.png){kind=logo}
Two related male patients with mesangiocapillary glomerulonephritis (MCGN) are described demonstrated by renal biopsy, inherited as an X-linked disorder. Family investigations failed to reveal any underlying immunological defects or a marker for the female carrier state. The age at diagnosis, the result of discovery of proteinuria on routine urine testing during infancy, is earlier than in any other reported cases of MCGN. This raises the possibility that this variety of MCGN may develop in utero and be detectable by alpha-fetoprotein maternal screening.
Related Publications
P R Stutchfield, and
R H White, and
A H Cameron, and
R A Thompson, and
P Mackintosh, and
L Wells
April 1992,
Journal of the American Society of Nephrology : JASN,
P R Stutchfield, and
R H White, and
A H Cameron, and
R A Thompson, and
P Mackintosh, and
L Wells
January 2001,
Terapevticheskii arkhiv,
P R Stutchfield, and
R H White, and
A H Cameron, and
R A Thompson, and
P Mackintosh, and
L Wells
June 1996,
Orvosi hetilap,
P R Stutchfield, and
R H White, and
A H Cameron, and
R A Thompson, and
P Mackintosh, and
L Wells
January 1987,
Arkhiv patologii,
P R Stutchfield, and
R H White, and
A H Cameron, and
R A Thompson, and
P Mackintosh, and
L Wells
April 1987,
Klinicheskaia meditsina,
P R Stutchfield, and
R H White, and
A H Cameron, and
R A Thompson, and
P Mackintosh, and
L Wells
January 1989,
Morphologiai es igazsagugyi orvosi szemle,
P R Stutchfield, and
R H White, and
A H Cameron, and
R A Thompson, and
P Mackintosh, and
L Wells
June 1976,
Harefuah,
P R Stutchfield, and
R H White, and
A H Cameron, and
R A Thompson, and
P Mackintosh, and
L Wells
January 1991,
American journal of nephrology,
P R Stutchfield, and
R H White, and
A H Cameron, and
R A Thompson, and
P Mackintosh, and
L Wells
November 1989,
The British journal of ophthalmology,
P R Stutchfield, and
R H White, and
A H Cameron, and
R A Thompson, and
P Mackintosh, and
L Wells
January 1973,
Perspectives in nephrology and hypertension,
