Abstract
Leroy syndrome, inclusion-cell disease (I-cell disease) or mucolipidosis II, is an autosomal recessive oligosaccharidosis, which is characterised by stunted stature, psychomotor retardation, coarse facies, rigid joints and skeletal deformities.
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Reference
Leroy JG, DeMars RI, Opitz JM (1969) I-cell disease. Birth Defects: Original Article Series V(4): 174–185
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© 1997 Springer-Verlag London Limited
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Beighton, P., Beighton, G. (1997). Leroy, J.G.. In: The Person Behind the Syndrome. Springer, London. https://doi.org/10.1007/978-1-4471-0925-9_141
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DOI: https://doi.org/10.1007/978-1-4471-0925-9_141
Publisher Name: Springer, London
Print ISBN: 978-1-4471-1236-5
Online ISBN: 978-1-4471-0925-9
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