Hurler's syndrome
- noun
- /ˈhɜr.lərz ˈsɪn.droʊm/
- Specialized
- Doctors diagnosed him with Hurler's syndrome after observing distinct skeletal abnormalities and developmental delays.
Examples
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Treatment for Hurler's syndrome often includes enzyme replacement therapy and sometimes bone marrow transplants.
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Children affected by Hurler's syndrome may show symptoms within their first year of life.
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Children with Hurler's syndrome often require specialized care.
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The doctor diagnosed him with Hurler's syndrome last week.
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Children affected by Hurler's syndrome may show symptoms within their first year of life.
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Doctors diagnosed him with Hurler's syndrome after observing distinct skeletal abnormalities and developmental delays.
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Treatment for Hurler's syndrome often includes enzyme replacement therapy and sometimes bone marrow transplants.
Synonyms
A rare inherited disease that causes abnormal bone and cartilage growth and learning difficulties
A condition that runs in families and causes severe bone and cartilage problems and slow development
An inherited disease that causes severe bone problems and learning difficulties
A rare inherited condition that causes severe bone problems and often learning difficulties
Surface Forms
Morphology
Hurler's + syndrome
The element 'syndrome' clearly signals a medical condition, so a learner who knows the constituents can infer this is some kind of disorder; however 'Hurler's' is a proper name with no lexical meaning for the learner and does not indicate the enzyme deficiency, developmental, skeletal or cognitive features. Because the overall specific meaning and cause are not derivable from the parts (only the general category is), the expression is only partially predictable to a B1 learner.
Etymology
Hurler's syndrome is named after Dr. Gertrud Hurler, the doctor who first wrote about children with this condition, so the name is a simple label tied to her work. Thinking of Dr. Hurler studying children with weak bones and learning problems helps you remember that the term refers to a rare disorder that causes 'abnormal development of bones, cartilage, and mental function'.