Galloway-Mowat syndrome
JCPSP-Journal of the College of Physicians and Surgeons Pakistan. 2008; 18 (8): 520-521
in English
| IMEMR
| ID: emr-102933
ABSTRACT
Galloway-Mowat syndrome is a rare multisystem genetic disorder with constellation of neurological, skeletal, growth, facial, gastrointestinal and renal abnormalities. This case report describes Galloway-Mowat syndrome in a young boy suffering from congenital microcephaly, developmental delay, seizures and various dysmorphic features in whom nephritic syndrome became apparent at 5 years of age
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Index:
IMEMR (Eastern Mediterranean)
Main subject:
Seizures
/
Abnormalities, Multiple
/
Fetal Growth Retardation
/
Genetic Diseases, Inborn
/
Hernia, Hiatal
/
Microcephaly
/
Nephrotic Syndrome
Type of study:
Case report
Limits:
Female
/
Humans
/
Male
Language:
English
Journal:
J. Coll. Physicians Surg. Pak.
Year:
2008
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