Curth Macklin syndrome, also known as ichthyosis hystrix, Curth-Macklin type, is a rare, inherited genetic skin disorder characterized by varying degrees of scaling skin (ichthyosis).
Here's a breakdown of the syndrome:
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Nature of the Disorder: It's a type of ichthyosis, meaning it's defined by abnormal scaling and thickening of the skin.
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Severity: The severity of the scaling can range from mild to severe. Some individuals may have small patches of scaly skin, while others may have widespread, thick scales covering much of their body.
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Appearance: The scaly patches can appear on almost any part of the body.
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Inheritance: It's an inherited disorder, meaning it's passed down through families via genes.
In essence, Curth Macklin syndrome is a genetic condition that manifests as abnormal, scaly skin, with the extent and severity of the scaling differing among affected individuals.
