Galloway-mowat syndrome-unusual form of nephrotic syndrome in adolescent
Joint Authors
Naidu, G. Diwakar
Deepthi, Pathapati
RajaKarthik, K.
Gangadhar, T.
Swarnalatha, G.
Sriram, S.
Source
Saudi Journal of Kidney Diseases and Transplantation
Issue
Vol. 28, Issue 5 (31 Oct. 2017), pp.1188-1191, 4 p.
Publisher
Saudi Center for Organ Transplantation
Publication Date
2017-10-31
Country of Publication
Saudi Arabia
No. of Pages
4
Main Subjects
Topics
Abstract EN
Galloway–Mowat syndrome (GMS), also acknowledged as Microcephaly-Hiatal hernia nephrotic syndrome, is an uncommon genetic disorder inherited as an autosomal recessive trait usually seen before two years of life.
It is an exceptional multisystem genetic disorder with a collection of skeletal, neurological, facial, gastrointestinal, growth, and renal abnormalities.
This case report describes GMS in a girl, suffering from developmental delay, stunted growth, and various dysmorphic features, in whom nephrotic syndrome became apparent at adolescent age.
American Psychological Association (APA)
Naidu, G. Diwakar& Deepthi, Pathapati& RajaKarthik, K.& Sriram, S.& Swarnalatha, G.& Gangadhar, T.. 2017. Galloway-mowat syndrome-unusual form of nephrotic syndrome in adolescent. Saudi Journal of Kidney Diseases and Transplantation،Vol. 28, no. 5, pp.1188-1191.
https://search.emarefa.net/detail/BIM-776967
Modern Language Association (MLA)
Naidu, G. Diwakar…[et al.]. Galloway-mowat syndrome-unusual form of nephrotic syndrome in adolescent. Saudi Journal of Kidney Diseases and Transplantation Vol. 28, no. 5 (Sep. / Oct. 2017), pp.1188-1191.
https://search.emarefa.net/detail/BIM-776967
American Medical Association (AMA)
Naidu, G. Diwakar& Deepthi, Pathapati& RajaKarthik, K.& Sriram, S.& Swarnalatha, G.& Gangadhar, T.. Galloway-mowat syndrome-unusual form of nephrotic syndrome in adolescent. Saudi Journal of Kidney Diseases and Transplantation. 2017. Vol. 28, no. 5, pp.1188-1191.
https://search.emarefa.net/detail/BIM-776967
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references : p. 1190-1191
Record ID
BIM-776967