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

Medicine

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