Muscle Biopsy as a Decisive Tool in a Pediatric Case with Overlapping
Genetic Findings for McArdle Disease and Dystrophinopathy
Muskelbiopsie als entscheidendes Instrument in einem
pädiatrischen Fall mit überlappenden genetischen Befunden für Morbus McArdle und
Dystrophinopathie
Authors
Esra Sayar
1
Department of Pediatrics, Metabolism Unit, Ankara Etlik City Hospital,
Ankara, Turkey
Mustafa Kılıç
2
Department of Pediatrics, Metabolism Unit, University of Health Sciences,
Ankara Etlik City Hospital, Ankara, Turkey
Suzan İcil
1
Department of Pediatrics, Metabolism Unit, Ankara Etlik City Hospital,
Ankara, Turkey
Pınar Saka-Ümit
3
Department of Pediatrics, Neurology Unit, Ankara Etlik City Hospital,
Ankara, Turkey
Deniz Yuksel
4
Department of Pediatrics, Neurology Unit, University of Health Sciences,
Ankara Etlik City Hospital, Ankara, Turkey
Abdullah Sezer
5
Department of Medical Genetics, Ankara Etlik City Hospital, Ankara,
Turkey
Beril Talim
6
Department of Pediatrics, Pathology Unit, Hacettepe University Faculty of
Medicine, Ankara, Turkey
