Erratum to: Glomerulopathy in patients with distal duplication of chromosome 6p
نویسندگان
چکیده
Author details Vilnius University, Children hospital affiliate of Vilnius university hospital “Santariskiu klinikos”, Santariskiu 4, Vilnius, LT 08406, Lithuania. Department of Biology and Genetics, Medical University of Gdańsk, Dębinki 1, Gdańsk 80211, Poland. Department of Pediatrics, Oslo University Hospital, Oslo, Norway. Department of Medical Genetics, Institute of Mother and Child, Warsaw, Poland. Division of Pediatric Nephrology, Center for Pediatrics and Adolescent Medicine, Heidelberg, Germany.
منابع مشابه
Glomerulopathy in patients with distal duplication of chromosome 6p.
BACKGROUND Duplication of the distal part of chromosome 6p is a rare genetic syndrome. Renal involvement has been reported in the majority of patients, including a wide range of congenital abnormalities of kidney and urinary tract and, occasionally, a proteinuric glomerulopathy. CASE PRESENTATION Here, we report a 13-year-old girl with 6p25.3p22.1 duplication who presented with proteinuria in...
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Chromosome 6p duplication is very rare and clinically characterized by short stature, mental retardation, and congenital heart diseases. Patients with mental retardation may present with poor oral health conditions. Dental treatment may need to be performed under general anesthesia in such patients. Our case report deals with induction of general anesthesia to a patient with chromosome 6p dupli...
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