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    Nakalanga Syndrome: Clinical Characteristics, Potential Causes, and Its Relationship with Recently Described Nodding Syndrome

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    Date
    2017
    Author
    FoÈger, Kathrin
    Gora-Stahlberg, Gina
    Sejvar, James
    Ovuga, Emilio
    ilek-Aall, Louise J
    Schmutzhard, Erich
    Kaiser, Christoph
    Winkler, Andrea S.
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    Abstract
    Nakalanga syndrome is a condition that was described in Uganda and various other African countries decades ago. Its features include growth retardation, physical deformities, endocrine dysfunction, mental impairment, and epilepsy, amongst others. Its cause remains obscure. Nodding syndrome is a neurological disorder with some features in common with Nakalanga syndrome, which has been described mainly in Uganda, South Sudan, and Tanzania. It has been considered an encephalopathy affecting children who, besides head nodding attacks, can also present with stunted growth, delayed puberty, and mental impairment, amongst other symptoms. Despite active research over the last years on the pathogenesis of Nodding syndrome, to date, no convincing single cause of Nodding syndrome has been reported. In this review, by means of a thorough literature search, we compare features of both disorders. We conclude that Nakalanga and Nodding syndromes are closely related and may represent the same condition. Our findings may provide new directions in research on the cause underlying this neurological disorder.
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    https://nru.uncst.go.ug/handle/123456789/4444
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    • Medical and Health Sciences [2955]

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