Kartal, AyseAydin, Kursad2020-03-262020-03-2620161971-40092385-1996https://dx.doi.org/10.1177/1971400916665371https://hdl.handle.net/20.500.12395/33319Aspartylglucosaminuria is a rare lysosomal storage disorder that occurs as a result of a deficiency of the aspartylglucosaminidase enzyme. Because the disease is commonly referred to as the Finnish disease heritage, it is underdiagnosed outside of Finland. To date, only three Turkish patients are described in the literature. Here we describe the clinical and brain magnetic resonance imaging findings in two Turkish cousins with aspartylglucosaminuria, which can raise the suspicion of this rare disease in clinical practice.en10.1177/1971400916665371info:eu-repo/semantics/openAccessAspartylglucosaminurialysosomal storage disorderbrain MRIArticle29531031327549151Q3WOS:000384443500003N/A