Vertical supranuclear gaze palsy (VSGP) is a key clinical feature in patients with Niemann-Pick type C disease (NP-C), a rare, autosomal recessive, neuro-visceral disorder caused by mutations in either the NPC1 or NPC2 gene. VSGP is present in approximately 65 % of the cases and is, with gelastic cataplexy, an important risk indicator for NP-C. VSGP in NP-C is characterized by a paralysis of vertical saccades, especially downward, with the slow vertical eye movement systems (smooth pursuit and the vestibulo-ocular reflex) spared in the early phase of the disease. This dissociation is caused by a selective vulnerability of the neurons in the rostral interstitial nuclei of the medial longitudinal fasciculus (riMLF) in NP-C. Here we discuss VSGP in NP-C and how clinicians can best elicit this sign.

Salsano, E., Umeh, C., Rufa, A., Pareyson, D., Zee, D.s. (2012). Vertical supranuclear gaze palsy in Niemann-Pick type C disease. NEUROLOGICAL SCIENCES, 33(6), 1225-1232 [10.1007/s10072-012-1155-1].

Vertical supranuclear gaze palsy in Niemann-Pick type C disease.

RUFA, ALESSANDRA;
2012-01-01

Abstract

Vertical supranuclear gaze palsy (VSGP) is a key clinical feature in patients with Niemann-Pick type C disease (NP-C), a rare, autosomal recessive, neuro-visceral disorder caused by mutations in either the NPC1 or NPC2 gene. VSGP is present in approximately 65 % of the cases and is, with gelastic cataplexy, an important risk indicator for NP-C. VSGP in NP-C is characterized by a paralysis of vertical saccades, especially downward, with the slow vertical eye movement systems (smooth pursuit and the vestibulo-ocular reflex) spared in the early phase of the disease. This dissociation is caused by a selective vulnerability of the neurons in the rostral interstitial nuclei of the medial longitudinal fasciculus (riMLF) in NP-C. Here we discuss VSGP in NP-C and how clinicians can best elicit this sign.
2012
Salsano, E., Umeh, C., Rufa, A., Pareyson, D., Zee, D.s. (2012). Vertical supranuclear gaze palsy in Niemann-Pick type C disease. NEUROLOGICAL SCIENCES, 33(6), 1225-1232 [10.1007/s10072-012-1155-1].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11365/37032
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