Syringomyelia in mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome): Imaging findings following bone marrow transplantation

Stephen H. Hite; William Krivit; Stephen J. Haines; Chester B. Whitley

doi:10.1007/s002470050213

Syringomyelia in mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome): Imaging findings following bone marrow transplantation

Stephen H. Hite
, William Krivit
, Stephen J. Haines
, Chester B. Whitley

Pediatric Genetics & Metabolism

Research output: Contribution to journal › Article › peer-review

13 Scopus citations

Abstract

We present the imaging findings in a patient with mucopolysaccharidosis (MPS) type VI (Maroteaux-Lamy syndrome) who developed holocord syringomyelia. This represents the only reported case of syrinx formation in a child with MPS VI. Clinical, neurologic and spinal magnetic resonance imaging findings are presented. The patient has maintained a stable clinical and neurologic course over the period following allogeneic bone marrow transplant.

Original language	English (US)
Pages (from-to)	736-738
Number of pages	3
Journal	Pediatric Radiology
Volume	27
Issue number	9
DOIs	https://doi.org/10.1007/s002470050213
State	Published - Sep 1997

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

Publisher link

10.1007/s002470050213

Find It

Find It at U of M Libraries

Cite this

@article{11a4494d98714508817ec83cec96bd6e,

title = "Syringomyelia in mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome): Imaging findings following bone marrow transplantation",

abstract = "We present the imaging findings in a patient with mucopolysaccharidosis (MPS) type VI (Maroteaux-Lamy syndrome) who developed holocord syringomyelia. This represents the only reported case of syrinx formation in a child with MPS VI. Clinical, neurologic and spinal magnetic resonance imaging findings are presented. The patient has maintained a stable clinical and neurologic course over the period following allogeneic bone marrow transplant.",

author = "Hite, \{Stephen H.\} and William Krivit and Haines, \{Stephen J.\} and Whitley, \{Chester B.\}",

year = "1997",

month = sep,

doi = "10.1007/s002470050213",

language = "English (US)",

volume = "27",

pages = "736--738",

journal = "Pediatric Radiology",

issn = "0301-0449",

publisher = "Springer Nature",

number = "9",

}

TY - JOUR

T1 - Syringomyelia in mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome)

T2 - Imaging findings following bone marrow transplantation

AU - Hite, Stephen H.

AU - Krivit, William

AU - Haines, Stephen J.

AU - Whitley, Chester B.

PY - 1997/9

Y1 - 1997/9

N2 - We present the imaging findings in a patient with mucopolysaccharidosis (MPS) type VI (Maroteaux-Lamy syndrome) who developed holocord syringomyelia. This represents the only reported case of syrinx formation in a child with MPS VI. Clinical, neurologic and spinal magnetic resonance imaging findings are presented. The patient has maintained a stable clinical and neurologic course over the period following allogeneic bone marrow transplant.

AB - We present the imaging findings in a patient with mucopolysaccharidosis (MPS) type VI (Maroteaux-Lamy syndrome) who developed holocord syringomyelia. This represents the only reported case of syrinx formation in a child with MPS VI. Clinical, neurologic and spinal magnetic resonance imaging findings are presented. The patient has maintained a stable clinical and neurologic course over the period following allogeneic bone marrow transplant.

UR - https://www.scopus.com/pages/publications/0030882718

UR - https://www.scopus.com/pages/publications/0030882718#tab=citedBy

U2 - 10.1007/s002470050213

DO - 10.1007/s002470050213

M3 - Article

C2 - 9285734

AN - SCOPUS:0030882718

SN - 0301-0449

VL - 27

SP - 736

EP - 738

JO - Pediatric Radiology

JF - Pediatric Radiology

IS - 9

ER -

Syringomyelia in mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome): Imaging findings following bone marrow transplantation

Abstract

UN SDGs

Publisher link

Find It

Other files and links

Fingerprint

Cite this