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黏脂贮积症III型的一种非典型形式。

An atypical form of mucolipidosis III.

作者信息

Freisinger P, Padovani J C, Maroteaux P

机构信息

Hôpital des Enfants Malades, Paris, France.

出版信息

J Med Genet. 1992 Nov;29(11):834-6. doi: 10.1136/jmg.29.11.834.

DOI:10.1136/jmg.29.11.834
PMID:1453439
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1016184/
Abstract

We report two sibs showing a very mild form of mucolipidosis III with no clinical signs but isolated involvement of the hip and very mild abnormalities of the spine. This indicates that a storage disease, in particular mucolipidosis III, should be considered in any case of isolated bilateral hip dysplasia. The differences from other reported atypical variants of mucolipidosis III are discussed.

摘要

我们报告了两名患有非常轻微形式的黏脂贮积症III型的同胞,他们没有临床症状,但仅髋关节受累,脊柱有非常轻微的异常。这表明,在任何孤立性双侧髋关节发育不良的病例中,都应考虑贮积病,尤其是黏脂贮积症III型。文中还讨论了与其他已报道的黏脂贮积症III型非典型变体的差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/faa0/1016184/a67141e6f709/jmedgene00025-0077-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/faa0/1016184/ee2590a3fefa/jmedgene00025-0076-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/faa0/1016184/a67141e6f709/jmedgene00025-0077-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/faa0/1016184/ee2590a3fefa/jmedgene00025-0076-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/faa0/1016184/a67141e6f709/jmedgene00025-0077-a.jpg

相似文献

1
An atypical form of mucolipidosis III.黏脂贮积症III型的一种非典型形式。
J Med Genet. 1992 Nov;29(11):834-6. doi: 10.1136/jmg.29.11.834.
2
MRI appearances of hip abnormalities in mucolipidosis, type III.III型黏脂贮积症中髋关节异常的磁共振成像表现
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3
[Three cases of mucolipidosis III with significant differences in clinical pictures--reevaluation of the classification of mucolipidosis II and III].三例临床表现差异显著的黏脂贮积症III型——对黏脂贮积症II型和III型分类的重新评估
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Mucolipidosis III presenting as a rheumatological disorder.表现为风湿性疾病的Ⅲ型粘脂贮积症。
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Mild I-cell disease, or severe pseudo-Hurler polydystrophy in three siblings: further evidence for intermediate forms of mucolipidosis II and III. Radiological features.轻度I型细胞病,或三例兄弟姐妹中的严重假性Hurler多营养不良:黏脂贮积症II型和III型中间形式的进一步证据。放射学特征。
Radiol Med. 1991 Dec;82(6):847-51.
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[Mucolipidosis: clinical and genetic aspects].[黏脂贮积症:临床与遗传学方面]
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Molecular order in mucolipidosis II and III nomenclature.黏脂贮积症II型和III型命名中的分子秩序
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Hip disease in Mucopolysaccharidoses and Mucolipidoses: A review of mechanisms, interventions and future perspectives.黏多糖贮积症和黏脂贮积症的髋关节病:发病机制、干预措施及未来展望的综述
Bone. 2021 Feb;143:115729. doi: 10.1016/j.bone.2020.115729. Epub 2020 Oct 29.
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Orthopaedic management in four cases of mucolipidosis type III.4例Ⅲ型黏脂贮积症的骨科治疗
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引用本文的文献

1
Mucolipidosis type III, a series of adult patients.黏脂贮积症 III 型,一系列成年患者。
J Inherit Metab Dis. 2018 Sep;41(5):839-848. doi: 10.1007/s10545-018-0186-z. Epub 2018 Apr 27.
2
Molecular analysis of the GlcNac-1-phosphotransferase.糖基转移酶的分子分析。
J Inherit Metab Dis. 2008 Apr;31(2):253-7. doi: 10.1007/s10545-008-0862-5. Epub 2008 Apr 15.

本文引用的文献

1
[Atypical spondylo-epiphysial dysplasia in 2 brothers].[两兄弟中的非典型脊椎骨骺发育不良]
Arch Fr Pediatr. 1957;14(5):506-10.
2
Mucolipidosis III is genetically heterogeneous.黏脂贮积症III型在遗传上具有异质性。
Proc Natl Acad Sci U S A. 1982 Dec;79(23):7420-4. doi: 10.1073/pnas.79.23.7420.
3
Phosphorylation of lysosomal enzymes in fibroblasts. Marked deficiency of N-acetylglucosamine-1-phosphotransferase in fibroblasts of patients with mucolipidosis III.成纤维细胞中溶酶体酶的磷酸化。黏脂贮积症III型患者成纤维细胞中N-乙酰葡糖胺-1-磷酸转移酶明显缺乏。
Hoppe Seylers Z Physiol Chem. 1982 Feb;363(2):169-78. doi: 10.1515/bchm2.1982.363.1.169.
4
Lysosomal enzyme targeting. N-Acetylglucosaminylphosphotransferase selectively phosphorylates native lysosomal enzymes.溶酶体酶靶向作用。N-乙酰葡糖胺磷酸转移酶选择性地使天然溶酶体酶磷酸化。
J Biol Chem. 1981 Dec 10;256(23):11977-80.
5
[Hurler's pseudo-polydystrophy].[胡勒氏假性多营养不良症]
Presse Med (1893). 1966 Dec 25;74(55):2889-92.
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Roentgen findings in mucolipidosis III (Pseudo-Hurler polydystrophy).
Radiology. 1973 Jan;106(1):153-60. doi: 10.1148/106.1.153.
7
The genetic mucolipidoses. Diagnosis and differential diagnosis.遗传性黏脂贮积症。诊断与鉴别诊断。
Humangenetik. 1970;9(2):113-39. doi: 10.1007/BF00278928.
8
Heterogeneity of N-acetylglucosamine 1-phosphotransferase within mucolipidosis III.黏脂贮积症III型中N-乙酰葡糖胺1-磷酸转移酶的异质性
J Biol Chem. 1986 Jan 15;261(2):733-8.
9
Mucolipidosis III (pseudo-Hurler polydystrophy): Clinical and laboratory studies in a series of 12 patients.黏脂贮积症III型(假性胡尔勒氏多营养不良):12例患者的临床与实验室研究
Johns Hopkins Med J. 1975 Oct;137(4):156-75.