Hypophosphatemia with reversible ataxia and quadriparesis

M. Rosenberg; J. R. McCarten; B. D. Snyder; J. W. Tulloch

doi:10.1097/00000441-198704000-00010

Hypophosphatemia with reversible ataxia and quadriparesis

M. Rosenberg, J. R. McCarten, B. D. Snyder, J. W. Tulloch

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Abstract

A malnourished alcoholic man with severe hypophosphatemia developed ataxia, severe proprioceptive deficit, and quadriparesis that worsened during refeeding. Evoked response and EMG studies demonstrated the central location of the rapidly reversible conduction block. This syndrome can mimic a number of entities including the Landry-Guillain-Barre (LGB) syndrome, acute brainstem disease, and certain deficiency states. The neurologic features of hypophosphatemia are reviewed.

Original language	English (US)
Pages (from-to)	261-264
Number of pages	4
Journal	American Journal of the Medical Sciences
Volume	293
Issue number	4
DOIs	https://doi.org/10.1097/00000441-198704000-00010
State	Published - 1987

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title = "Hypophosphatemia with reversible ataxia and quadriparesis",

abstract = "A malnourished alcoholic man with severe hypophosphatemia developed ataxia, severe proprioceptive deficit, and quadriparesis that worsened during refeeding. Evoked response and EMG studies demonstrated the central location of the rapidly reversible conduction block. This syndrome can mimic a number of entities including the Landry-Guillain-Barre (LGB) syndrome, acute brainstem disease, and certain deficiency states. The neurologic features of hypophosphatemia are reviewed.",

author = "M. Rosenberg and McCarten, {J. R.} and Snyder, {B. D.} and Tulloch, {J. W.}",

year = "1987",

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AU - Rosenberg, M.

AU - McCarten, J. R.

AU - Snyder, B. D.

AU - Tulloch, J. W.

PY - 1987

Y1 - 1987

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AB - A malnourished alcoholic man with severe hypophosphatemia developed ataxia, severe proprioceptive deficit, and quadriparesis that worsened during refeeding. Evoked response and EMG studies demonstrated the central location of the rapidly reversible conduction block. This syndrome can mimic a number of entities including the Landry-Guillain-Barre (LGB) syndrome, acute brainstem disease, and certain deficiency states. The neurologic features of hypophosphatemia are reviewed.

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JO - American Journal of the Medical Sciences

JF - American Journal of the Medical Sciences

IS - 4

ER -

Hypophosphatemia with reversible ataxia and quadriparesis

Abstract

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