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Neuronal Ceroid Lipofuscinosis With Hypergonadotropic Hypogonadism

Department of Neurology, The New York Hospital-Cornell Medical Center

Carol Petito, MD

Department of Neurology, The New York Hospital-Cornell Medical Center, Department of Pathology, The New York Hospital-Cornell Medical Center, New York, NY

Elizabeth Stoner, MD

Department of Pediatrics, The New York Hospital-Cornell Medical

Maria New, MD

Department of Pediatrics, The New York Hospital-Cornell Medical

A case of adolescent-onset neuronal ceroid lipofuscinosis presenting with chorea and evidencing pyramidal and cerebellar dysfunction as well as hypergonadotropic hypogonadism is reported. In this patient, primary ovarian failure may be due to accumulation of ceroid in the ovaries. ( J Child Neurol 1986; 1:142-144)

Journal of Child Neurology, Vol. 1, No. 2, 142-144 (1986)
DOI: 10.1177/088307388600100209


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