Volume : III, Issue : V, May - 2014
HYDRONEPHROSIS IMPORTANT FOR DIAGNOSIS IN SCHINZEL–GIEDION SYNDROME
Dr. Abnish Kumar, Dr. Manoj Kumar Singh, Dr. Neeraj Yadav, Dr. Parveen Kumar
Abstract :
Schinzel–Giedion syndrome is a rare autosomal recessive disorder characterized by coarse facies, midfaceretraction, hypertrichosis, multiple skeletal anomalies, and cardiac and renal malformations. Craniofacial abnormalities of this syndrome sometimes resemble a storage or metabolic disease. The pathogenesis of the disease remains unknown.The objective of this report was to emphasize the importance of congenital bilateral hydronephrosis for the diagnosisof Schinzel–Giedion syndrome.
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DOI : 10.36106/ijsr
Cite This Article:
DR. ABNISH KUMAR, DR. MANOJ KUMAR SINGH, DR. NEERAJ YADAV, DR. PARVEEN KUMAR /HYDRONEPHROSIS IMPORTANT FOR DIAGNOSIS IN SCHINZEL-GIEDION SYNDROME /International Journal of Scientific Research, Vol.3, Issue. 5, May 2014
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DR. ABNISH KUMAR, DR. MANOJ KUMAR SINGH, DR. NEERAJ YADAV, DR. PARVEEN KUMAR /HYDRONEPHROSIS IMPORTANT FOR DIAGNOSIS IN SCHINZEL-GIEDION SYNDROME /International Journal of Scientific Research, Vol.3, Issue. 5, May 2014
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