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Am J Med Genet A. 2016 May;170A(5):1187-95. doi: 10.1002/ajmg.a.37543. Epub 2016 Jan 8.

Renal involvement in patients with mucolipidosis IIIalpha/beta: Causal relation or co-occurrence?

Author information

1
Department of Pediatric Genetics, Cerrahpasa Medical School, Istanbul University, Istanbul, Turkey.
2
Department of Neurosurgery, Program on Neurogenetics, Yale School of Medicine, New Haven, Connecticut.
3
Department of Pediatric Nephrology, Cerrahpasa Medical School, Istanbul University, Istanbul, Turkey.
4
Department of Pathology, Istanbul Medical School, Istanbul University, Istanbul, Turkey.

Abstract

Mucolipidosis IIIalpha/beta (MLIIIalpha/beta) is a rare lysosomal storage disorder characterized by childhood onset of flexion contractures of fingers, joint stiffness in the shoulders, hips, and knees, and mild short stature. Recessive mutations in the GNPTAB gene have been associated with MLIIIalpha/beta. We present five children aged 9-16 years from a large kindred family whose serum activities of several lysosomal enzymes were significantly elevated. Whole exome sequencing followed by confirmation by Sanger sequencing identified a novel homozygous missense mutation (c.22 A > G; p.R8G) in the GNPTAB gene in all affected subjects. The five patients initially presented with flexion contractures of fingers followed by stiffnes of large joints. Only two affected boys also had a nephrotic-range proteinuria. Renal biopsy showed focal segmental glomerulosclerosis and foamy appearance of glomerular visceral epithelial cells which were compatible with storage disease. No other known causes of proteinuria could be detected by both laboratory and biopsy findings. There was no known family history of hereditary kidney disease, and healthy siblings and parents had normal renal function and urinalysis. These findings suggest that the renal involvement probably due to MLIIIalpha/beta, although it can still be present by coincidence in the two affected patients.

KEYWORDS:

GNPTAB gene; mucolipidosis IIIalpha/beta; renal involvement

PMID:
26749367
DOI:
10.1002/ajmg.a.37543
[Indexed for MEDLINE]

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