Familial progressive neuronal disease and chronic idiopathic intestinal pseudo-obstruction

I. Steiner; A. Steinberg; Z. Argov; J. Faber; A. Fich; A. Gilai

doi:10.1212/wnl.37.6.1046

Familial progressive neuronal disease and chronic idiopathic intestinal pseudo-obstruction

I. Steiner^*, A. Steinberg, Z. Argov, J. Faber, A. Fich, A. Gilai

^*Corresponding author for this work

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Abstract

Chronic idiopathic intestinal pseudo-obstruction (CIIP) is characterized by recurrent episodes of bowel obstruction without mechanical cause. In five members of two Jewish-Iranian families, CIIP was associated with progressive neuronal disease, starting before age 30, with ophthalmoplegia, sensorimotor peripheral neuropathy, and hearing loss. There was no evidence of CNS involvement. The pattern suggested autosomal recessive inheritance.

Original language	English
Pages (from-to)	1046-1050
Number of pages	5
Journal	Neurology
Volume	37
Issue number	6
DOIs	https://doi.org/10.1212/wnl.37.6.1046
State	Published - Jun 1987
Externally published	Yes

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title = "Familial progressive neuronal disease and chronic idiopathic intestinal pseudo-obstruction",

abstract = "Chronic idiopathic intestinal pseudo-obstruction (CIIP) is characterized by recurrent episodes of bowel obstruction without mechanical cause. In five members of two Jewish-Iranian families, CIIP was associated with progressive neuronal disease, starting before age 30, with ophthalmoplegia, sensorimotor peripheral neuropathy, and hearing loss. There was no evidence of CNS involvement. The pattern suggested autosomal recessive inheritance.",

author = "I. Steiner and A. Steinberg and Z. Argov and J. Faber and A. Fich and A. Gilai",

year = "1987",

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AU - Steinberg, A.

AU - Argov, Z.

AU - Faber, J.

AU - Fich, A.

AU - Gilai, A.

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AB - Chronic idiopathic intestinal pseudo-obstruction (CIIP) is characterized by recurrent episodes of bowel obstruction without mechanical cause. In five members of two Jewish-Iranian families, CIIP was associated with progressive neuronal disease, starting before age 30, with ophthalmoplegia, sensorimotor peripheral neuropathy, and hearing loss. There was no evidence of CNS involvement. The pattern suggested autosomal recessive inheritance.

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Familial progressive neuronal disease and chronic idiopathic intestinal pseudo-obstruction

Abstract

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