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 |
| Published: |
SAGE Publishing,
2019-01-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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| Call Number: |
A1234.567 |
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| Copy 1 | Available |