Usefulness of bone marrow transplantation in the Hurler syndrome

Elizabeth A. Braunlin; Nanci R. Stauffer; Charles H. Peters; John L. Bass; James M. Berry; John J. Hopwood; William Krivit

doi:10.1016/S0002-9149(03)00909-3

Usefulness of bone marrow transplantation in the Hurler syndrome

Elizabeth A. Braunlin, Nanci R. Stauffer, Charles H. Peters, John L. Bass, James M. Berry, John J. Hopwood, William Krivit

Pediatric Cardiology

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Abstract

The Hurler syndrome, an autosomal recessive storage disease of childhood, leads to death within the first decade of life from progressive deposition of glycosaminoglycans within the myointima of the coronary arteries and airways. Cardiac ultrasound findings of patients with this syndrome >10 years after successful bone marrow transplantation are described.

Original language	English (US)
Pages (from-to)	882-886
Number of pages	5
Journal	American Journal of Cardiology
Volume	92
Issue number	7
DOIs	https://doi.org/10.1016/S0002-9149(03)00909-3
State	Published - Oct 1 2003

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10.1016/S0002-9149(03)00909-3

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title = "Usefulness of bone marrow transplantation in the Hurler syndrome",

abstract = "The Hurler syndrome, an autosomal recessive storage disease of childhood, leads to death within the first decade of life from progressive deposition of glycosaminoglycans within the myointima of the coronary arteries and airways. Cardiac ultrasound findings of patients with this syndrome >10 years after successful bone marrow transplantation are described.",

author = "Braunlin, {Elizabeth A.} and Stauffer, {Nanci R.} and Peters, {Charles H.} and Bass, {John L.} and Berry, {James M.} and Hopwood, {John J.} and William Krivit",

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AU - Peters, Charles H.

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AU - Berry, James M.

AU - Hopwood, John J.

AU - Krivit, William

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AB - The Hurler syndrome, an autosomal recessive storage disease of childhood, leads to death within the first decade of life from progressive deposition of glycosaminoglycans within the myointima of the coronary arteries and airways. Cardiac ultrasound findings of patients with this syndrome >10 years after successful bone marrow transplantation are described.

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Usefulness of bone marrow transplantation in the Hurler syndrome

Abstract

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