Muscle Hypotonia in Lowe’s Syndrome
Abstract
As part of a comprehensive evaluation of 23 patients with the oculocerebrorenal syndrome of Lowe at the Section on Human Biochemical Genetics, National Institutes of Health, Bethesda, MD, concentrations of muscle enzymes and carnitine metabolism were studied in addition to special reference to growth and renal function.
DOI: https://doi.org/10.15844/pedneurbriefs-5-6-4 | Journal eISSN: 2166-6482
Language: English
Page range: 43 - 44
Published on: Jun 1, 1991
Published by: Pediatric Neurology Briefs Publishers
In partnership with: Paradigm Publishing Services
© 1991 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.