Hip Morphology in Mucolipidosis Type II.

I-cell disease ML intermediate MLII cloaking femoral bowing hip hip dislocation hip dysplasia mucolipidosis type II ultrasound

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
08 Mar 2020
Historique:
received: 18 01 2020
revised: 02 03 2020
accepted: 06 03 2020
entrez: 19 3 2020
pubmed: 19 3 2020
medline: 19 3 2020
Statut: epublish

Résumé

Mucolipidosis type II (MLII) is a rare lysosomal storage disorder caused by defective trafficking of lysosomal enzymes. Severe skeletal manifestations are a hallmark of the disease including hip dysplasia. This study aims to describe hip morphology and the natural course of hip pathologies in MLII by systematic evaluation of plain radiographs, ultrasounds and magnetic resonance imaging (MRI). An international two-centered study was performed by retrospective chart review. All MLII patients with at least one pelvic radiograph were included. A total of 16 patients were followed over a mean of 3.5 years (range 0.2-10.7 years). Typical age-dependent radiographic signs identified were femoral cloaking (7/16), rickets/hyperparathyroidism-like changes (6/16) and constrictions of the supra-acetabular part of the os ilium (16/16) and the femoral neck (7/16). The course of acetabular and migration indexes (AI, MI) significantly increased in female patients. However, in the overall group, there was no relevant progression of acetabular dysplasia with a mean AI of 23.0 (range 5°-41°) and 23.7° (range 5°-40°) at the first and last assessments, respectively. Better knowledge on hip morphology in MLII could lead to earlier diagnosis, improved clinical management and enables assessment of effects of upcoming therapies on the skeletal system.

Identifiants

pubmed: 32182687
pii: jcm9030728
doi: 10.3390/jcm9030728
pmc: PMC7141371
pii:
doi:

Types de publication

Journal Article

Langues

eng

Références

Eur J Hum Genet. 2014 May;22(5):594-601
pubmed: 24045841
Science. 2011 Jul 1;333(6038):87-90
pubmed: 21719679
Acta Neuropathol. 1975 Dec 30;33(4):285-305
pubmed: 3084
Acta Orthop Scand Suppl. 1980;184:1-100
pubmed: 6930145
Pediatr Radiol. 2016 Nov;46(12):1713-1720
pubmed: 27525427
Nat Med. 2005 Oct;11(10):1109-12
pubmed: 16200072
Pediatrics. 1974 Dec;54(6):797-805
pubmed: 4372583
Clin Orthop Relat Res. 1992 Mar;(276):283-90
pubmed: 1537168
Am J Med Genet A. 2008 Feb 15;146A(4):512-3
pubmed: 18203164
Clin Orthop Relat Res. 1981 Oct;(160):14-29
pubmed: 7285414
Birth Defects Orig Artic Ser. 1975;11(6):283-93
pubmed: 1103995
J Pediatr Genet. 2019 Dec;8(4):198-204
pubmed: 31687257
Humangenetik. 1970;9(2):113-39
pubmed: 4246487
AJR Am J Roentgenol. 1977 Jul;129(1):37-43
pubmed: 409140
Eur J Cell Biol. 2010 Jan;89(1):117-23
pubmed: 19945768
Arch Orthop Trauma Surg. 1984;102(4):248-55
pubmed: 6712426
Clin Orthop Relat Res. 2015 Apr;473(4):1234-46
pubmed: 25384429
J Paediatr Child Health. 2010 Jun;46(6):316-22
pubmed: 20367762
Pediatr Radiol. 1989;19(6-7):406-13
pubmed: 2771479
Hum Mutat. 2019 Jul;40(7):842-864
pubmed: 30882951
Science. 1967 Aug 18;157(3790):804-6
pubmed: 17842782
J Pediatr Orthop. 2018 Mar;38(3):163-169
pubmed: 27261963
Clin Orthop Relat Res. 1976 Sep;(119):39-47
pubmed: 954321
Clin Genet. 1985 Sep;28(3):207-15
pubmed: 2998652
Am J Roentgenol Radium Ther Nucl Med. 1973 May;118(1):213-21
pubmed: 4267400
Orthop Clin North Am. 2006 Apr;37(2):119-32, v
pubmed: 16638443
Am J Dis Child. 1975 Sep;129(9):1083-90
pubmed: 1190182
Mol Genet Metab. 2006 Aug;88(4):359-63
pubmed: 16630736
Postgrad Med J. 1973 May;49(571):359-61
pubmed: 4216890
EMBO Mol Med. 2013 Dec;5(12):1871-86
pubmed: 24127423
J Med Genet. 2010 Jan;47(1):38-48
pubmed: 19617216
J Bone Joint Surg Br. 2010 Sep;92(9):1312-5
pubmed: 20798455
Clin Orthop Relat Res. 1984 Apr;(184):34-40
pubmed: 6705362

Auteurs

Luise Sophie Ammer (LS)

Department of Pediatrics, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
International Center for Lysosomal Disorders, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.

Esmeralda Oussoren (E)

Department of Pediatrics, Center for Lysosomal and Metabolic Diseases, Erasmus University Medical Center, 3015 GE Rotterdam, The Netherlands.

Nicole Maria Muschol (NM)

Department of Pediatrics, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
International Center for Lysosomal Disorders, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.

Sandra Pohl (S)

Department of Osteology and Biomechanics, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.

Maria Estela Rubio-Gozalbo (ME)

Department of Pediatrics and Clinical Genetics, Maastricht University Medical Center, 6211 LK Maastricht, The Netherlands.

René Santer (R)

Department of Pediatrics, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.

Ralf Stuecker (R)

International Center for Lysosomal Disorders, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
Department of Pediatric Orthopedics, Children's Hospital Altona, 22763 Hamburg, Germany.
Department of Orthopedics, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.

Eik Vettorazzi (E)

Department of Medical Biometry and Epidemiology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.

Sandra Rafaela Breyer (SR)

International Center for Lysosomal Disorders, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
Department of Pediatric Orthopedics, Children's Hospital Altona, 22763 Hamburg, Germany.
Department of Orthopedics, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.

Classifications MeSH