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January 1991, Vol 145, No. 1 >
Article | January 1991

Picture of the Month

Jeffrey L. Loughead, MD; Francis Mimouni, MD; Sue Schilling, RN; Murray Feingold, MD
Am J Dis Child. 1991;145(1):113-114. doi:10.1001/archpedi.1991.02160010119030.
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Denouement and Discussion 

Lowe's Syndrome  Lowe's syndrome, or oculocerebrorenal syndrome, is an X-linked hereditary disease characterized by congenital ocular disease, renal tubular dysfunction, hypotonia, moderate to severe bone disease, and mental retardation. It is present in all races, with a predominance in those with Caucasian and Asian ancestries.The disease has three identifiable stages. The first, during the newborn period, is characterized by ocular pathologic features. Nearly all affected individuals have congenital, ocular disease, renal tubular dysfunction, hypotonia, moderate to severe bone disease, and mental retardation. It is present in all races, with a predominance in those with Caucasian and Asian ancestries.

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Country-Specific Mortality and Growth Failure in Infancy and Yound Children and Association With Material Stature

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