Partial trisomy 13q22-qter associated to leukoencephalopathy and late onset generalised epilepsy
Renee Ribacoba1, Manuel Menendez-Gonzalez, Ines Hernando
1Unit of Neurology, Hospital Alvarez Buylla, Mieres, Spain. rribacoba@gmail.com.
Abstract:
The partial trisomy 13q.22 is an uncommon chromosomopathy. We present a case with a partial trisomic component 13q22 and a monosomic component 5p15 from paternal origin. This patient developed early menopause and major neurological disorders as leukoencephalopathy, late onset generalised epilepsy and stroke. She also had fatty acids disturbances and their potential relation to the neurological disorders and early menopause is discussed. The presented case illustrates the phenotype of 13q22-qter in adult age and reaffirms the importance of studying the karyotype of any patient with seizures or leukoencephalopathy particularly when there are associated other clinical features including stroke at a young age, fatty acids disturbances, microcephaly, hypotelorism, short neck, hemangiomata, short fingers or distal swell in thumbs.
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