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[Plexiform neurofibroma and basal ganglia anomaly in Watson syndrome]
P Weber1, S Kotthoff, G Schuierer
1Klinik und Poliklinik für Kinderheilkunde, Universitätsklinik Münster.
Klinische Padiatrie
|July 21, 1999
Abstract:
A 4 year-old boy was referred for diagnostic reevaluation with known pulmonary valve stenosis. Physical examination revealed multiple cafe-au-lait spots, inguinal freckling and on the right side in supraclavicular region a softly, non-painful tumour. The boy showed a mild mental and language retardation. Ultrasound and MRT demonstrated supraclavicular a plexiform neurofibroma and intracranial increased intensity lesions in basal ganglia and mesencephalon. In our patient, we have diagnosed a Watson-Syndrome, the overlap and differences to neurofibromatosis type I is discussed.