Severe Restrictive Lung Disease in One of the Oldest Documented Males With Coffin-Lowry Syndrome
Coffin-Lowry syndrome is expressed as different phenotypes in males and females. In males, it is characterized by facial abnormalities, marked developmental disability, and skeletal changes. Approximately 80% of cases are associated with kyphoscoliosis, which can be quite severe, as seen in our pati...
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| Main Authors: | , , , |
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| Format: | Book |
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SAGE Publishing,
2019-01-01T00:00:00Z.
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| Summary: | Coffin-Lowry syndrome is expressed as different phenotypes in males and females. In males, it is characterized by facial abnormalities, marked developmental disability, and skeletal changes. Approximately 80% of cases are associated with kyphoscoliosis, which can be quite severe, as seen in our patient, causing paraplegia and restrictive lung disease. In this article, we present the third oldest documented male case of Coffin-Lowry syndrome with severe kyphoscoliosis, paraplegia, and restrictive lung disease. |
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| Item Description: | 2324-7096 10.1177/2324709618820660 |