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CASE REPORT
Multicystic Renal Dysplasia in a Child with
Split Hand/Split Foot Malformation
1
Yüzüncü Yıl University, Faculty of
Medicine, Department of Pediatrics, Van,
Turkey
2
Konya Education and Research Hospital,
Department of Pediatrics, Konya, Turkey
Publication date: 2012-01-10
Corresponding author
Cihangir Akgün
University of Yüzüncü Yıl Faculty of Medicine, Department of Pediatric Nephrology, 65200, Van, Turkey
University of Yüzüncü Yıl Faculty of Medicine, Department of Pediatric Nephrology, 65200, Van, Turkey
Eur J Gen Med 2012;9(Supplement 1):30–32
KEYWORDS
ABSTRACT
Split hand/split foot malformation is a human developmental disorder
characterized by missing central digits and other distal limb malformations.
Multicystic renal dysplasia is the most common cause of
an abdominal mass in the new born period and is the most common
cystic malformation of the kidney in infancy. Here, we report a case
of split hand/split foot malformation with a submucosed cleft palate
and multicystic renal dysplasia in one-year old boy.
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