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

被引：0

作者：

S. H. Hite

William Krivit

Stephen J. Haines

Chester B. Whitley

机构：

[1] Department of Radiology,

[2] Box 292,undefined

[3] University of Minnesota Hospital and Clinic,undefined

[4] 420 Delaware Street SE,undefined

[5] Minneapolis,undefined

[6] MN 55455,undefined

[7] USA,undefined

[8] Department of Pediatrics and Institute for Human Genetics,undefined

[9] University of Minnesota Hospital and Clinic,undefined

[10] Minneapolis,undefined

[11] Minnesota,undefined

[12] USA,undefined

[13] Department of Neurological Surgery,undefined

[14] University of Minnesota Hospital and Clinic,undefined

[15] Minneapolis,undefined

[16] Minnesota,undefined

[17] USA,undefined

来源：

Pediatric Radiology | 1997年 / 27卷

关键词：

Magnetic Resonance Imaging; Bone Marrow; Bone Marrow Transplant; Marrow Transplant; Imaging Finding;

D O I：

暂无

中图分类号：

学科分类号：

摘要：

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.

引用

页码：736 / 738

页数：2

共 50 条

[31] Macrophage Involvement in Mitral Valve Pathology in Mucopolysaccharidosis Type VI (Maroteaux-Lamy Syndrome)
Brands, Marion
Roelants, Jorine
de Krijger, Ronald
Bogers, Ad
Reuser, Arnold
van der Ploeg, Ans
Helbing, Wim
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2013, 161 (10) : 2550 - 2553
[32] CLEARING OF THE HOST CORNEA FOLLOWING PENETRATING KERATOPLASTY IN PATIENTS WITH THE MAROTEAUX-LAMY SYNDROME (MUCOPOLYSACCHARIDOSIS TYPE-VI-A)
NAUMANN, GOH
RUMMELT, V
KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE, 1993, 203 (05) : 351 - 360
[33] Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome): defining and measuring functional impacts in pediatric patients
Beth Leiro
Dawn Phillips
Melanie Duiker
Paul Harmatz
Sharon Charles
Orphanet Journal of Rare Diseases, 16
[34] Umbilical cord blood transplantation for Maroteaux–Lamy syndrome (mucopolysaccharidosis type VI)
V Lee
CK Li
MMK Shing
KW Chik
CW Lam
KS Tsang
H Pong
KF Huen
PMP Yuen
Bone Marrow Transplantation, 2000, 26 : 455 - 458
[35] OCCURRENCE OF MULTIPLE DENTIGEROUS CYSTS IN A PATIENT WITH THE MAROTEAUX-LAMY SYNDROME (MUCOPOLYSACCHARIDOSIS, TYPE-VI)
ROBERTS, MW
BARTON, NW
CONSTANTOPOULOS, G
BUTLER, DP
DONAHUE, AH
ORAL SURGERY ORAL MEDICINE ORAL PATHOLOGY ORAL RADIOLOGY AND ENDODONTOLOGY, 1984, 58 (02): : 169 - 175
[36] Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome): defining and measuring functional impacts in pediatric patients
Leiro, Beth
Phillips, Dawn
Duiker, Melanie
Harmatz, Paul
Charles, Sharon
ORPHANET JOURNAL OF RARE DISEASES, 2021, 16 (01)
[37] Mucopolysaccharidosis VI (Maroteaux-Lamy Syndrome): Development of Clinical and Laboratory Guidelines for Diagnosis
Harmatz, Paul
MOLECULAR GENETICS AND METABOLISM, 2012, 105 (02) : S33 - S33
[38] Clinical study of 10 Brazilian cases of mucopolysaccharidosis VI (Maroteaux-Lamy syndrome).
Kim, CA
Paula, AC
Bertola, DR
Toma, L
Giugliani, R
Moreira, MB
Ferraro, VH
Albano, LMJ
AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (05) : 452 - 452
[39] Corneal transplantation in Maroteaux-Lamy syndrome
Varssano, D
Cohen, EJ
Nelson, LB
Eagle, RC
ARCHIVES OF OPHTHALMOLOGY, 1997, 115 (03) : 428 - 429
[40] Abnormal neuronal metabolism and storage in mucopolysaccharidosis type VI (Maroteaux-Lamy) disease
Walkley, SU
Thrall, MA
Haskins, ME
Mitchell, TW
Wenger, DA
Brown, DE
Dial, S
Seim, H
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, 2005, 31 (05) : 536 - 544

← 1 2 3 4 5 →