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Genet Couns ; 27(4): 489-494, 2016.
Article in English | MEDLINE | ID: mdl-30226968

ABSTRACT

Pantothenate-kinase-associated neurodegeneration (PKAN) is a rare autosomal recessive disorder caused by mutations in the pantothenate kinase 2 (PANK2) gene. Many different mutations in the PANK2 gene have been detected in association with PKAN. A 20 year old female patient who had been suffering from progressive gait disorder for 1 year was found to have the 'eye-of-the-tiger sign' from the brain magnetic resonance imaging (MRI). The same brain imaging findings were shown in the father and brother of the patient, whose parents arranged a consanguineous marriage. We found c.966 G>T (p.Glu322Asp) mutation in the PANK2 gene mutation analysis in the individuals from the brain imaging findings. Although individuals in this family who had a homozygous mutation in PANK2 gene analyses had the 'eye-of-the-tiger' sign and atypical disease, they were noted to have differing clinical findings.


Subject(s)
DNA Mutational Analysis , Pantothenate Kinase-Associated Neurodegeneration/genetics , Phosphotransferases (Alcohol Group Acceptor)/genetics , Adult , Brain/pathology , Consanguinity , Female , Gait Disorders, Neurologic/diagnosis , Gait Disorders, Neurologic/genetics , Genotype , Globus Pallidus/pathology , Humans , Magnetic Resonance Imaging , Male , Middle Aged , Pantothenate Kinase-Associated Neurodegeneration/diagnosis , Pedigree , Phenotype , Turkey , Young Adult
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