A Variant Form of Mucolipidosis IV: Report on 4 Patients From the Indian Subcontinent

被引:8
作者
Bindu, Parayil Sankaran [1 ]
Gayathri, Narayanappa [2 ]
Yasha, Thagadur C. [2 ]
Kovoor, Jerry M. E. [3 ]
Subasree, Ramakrishnan [1 ]
Rao, Sudheendra [1 ]
Panda, Samhita [1 ]
Pal, Pramod Kumar [1 ]
机构
[1] Natl Inst Mental Hlth & Neurosci, Dept Neurol, Bangalore 560029, Karnataka, India
[2] Natl Inst Mental Hlth & Neurosci, Dept Neuropathol, Bangalore 560029, Karnataka, India
[3] Natl Inst Mental Hlth & Neurosci, Dept Neuroimaging & Intervent Radiol, Bangalore 560029, Karnataka, India
关键词
mucolipidosis IV; spastic paraplegia; lamellar inclusions; corpus callosum;
D O I
10.1177/0883073808318537
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The clinical manifestations and histopathologic and neuroimaging findings in 4 Indian patients with a variant form of mucolipidosis IV are described. The presenting symptoms were psychomotor delay, spastic paraplegia, and mild mental retardation. One patient also had visual deterioration due to optic atrophy. None had corneal or retinal abnormalities. Magnetic resonance imaging in 3 patients showed a uniformly thin corpus callosum in all patients and white matter changes in 2 patients. Electron microscopic examination of skin biopsy specimens revealed storage bodies characteristic of mucolipidosis IV These patients differ from previously described patients with this disorder in the absence of corneal abnormalities and in their presentation with spastic paraplegia during the second decade of life. Correct diagnosis is needed for genetic counseling, prognostication. and reduction of additional familial burden of this rare disease.
引用
收藏
页码:1443 / 1446
页数:4
相关论文
共 15 条
[1]   The neurogenetics of mucolipidosis type IV [J].
Altarescu, G ;
Sun, M ;
Moore, DF ;
Smith, JA ;
Wiggs, EA ;
Solomon, BI ;
Patronas, NJ ;
Frei, KP ;
Gupta, S ;
Kaneski, CR ;
Quarrell, OW ;
Slaugenhaupt, SA ;
Goldin, E ;
Schiffmann, R .
NEUROLOGY, 2002, 59 (03) :306-313
[2]  
AMIR N, 1987, PEDIATRICS, V79, P953
[3]   Mucolipidosis type IV [J].
Bach, G .
MOLECULAR GENETICS AND METABOLISM, 2001, 73 (03) :197-203
[4]   Identification of the gene causing mucolipidosis type IV [J].
Bargal, R ;
Avidan, N ;
Ben-Asher, E ;
Olender, Z ;
Zeigler, M ;
Frumkin, A ;
Raas-Rothschild, A ;
Glusman, G ;
Lancet, D ;
Bach, G .
NATURE GENETICS, 2000, 26 (01) :118-121
[5]  
Bass Nancy, 1999, Current Opinion in Pediatrics, V11, P504, DOI 10.1097/00008480-199912000-00005
[6]   CONGENITAL CORNEAL CLOUDING WITH ABNORMAL SYSTEMIC STORAGE BODIES - NEW VARIANT OF MUCOLIPIDOSIS [J].
BERMAN, ER ;
LIVNI, N ;
SHAPIRA, E ;
MERIN, S ;
LEVIJ, IS .
JOURNAL OF PEDIATRICS, 1974, 84 (04) :519-526
[7]   MUCOLIPIDOSIS TYPE-IV - CLINICAL MANIFESTATIONS AND NATURAL-HISTORY [J].
CHITAYAT, D ;
MEUNIER, CM ;
HODGKINSON, KA ;
SILVER, K ;
FLANDERS, M ;
ANDERSON, IJ ;
LITTLE, JM ;
WHITEMAN, DAH ;
CARPENTER, S .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1991, 41 (03) :313-318
[8]   MUCOLIPIDOSIS-IV [J].
CRANDALL, BF ;
PHILIPPART, M ;
BROWN, WJ ;
BLUESTONE, DA .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1982, 12 (03) :301-308
[9]   MUCOLIPIDOSIS-IV - MORPHOLOGY AND HISTOCHEMISTRY OF AN AUTOPSY CASE [J].
FOLKERTH, RD ;
ALROY, J ;
LOMAKINA, I ;
SKUTELSKY, E ;
RAGHAVAN, SS ;
KOLODNY, EH .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1995, 54 (02) :154-164
[10]   Mucolipidosis type IV - Characteristic MRI findings [J].
Frei, KP ;
Patronas, NJ ;
Crutchfield, KE ;
Altarescu, G ;
Schiffmann, R .
NEUROLOGY, 1998, 51 (02) :565-569