Spielmeyer-Vogt disease
- noun
- /ˈspiːlˌmaɪər ˈvoʊt dɪˈziːz/
- Specialized
- Doctors diagnosed the child with Spielmeyer-Vogt disease after he began to lose his vision and cognitive abilities.
Examples
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The symptoms of Spielmeyer-Vogt disease can appear as early as three years old.
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Because Spielmeyer-Vogt disease is inherited, genetic counseling was recommended for the affected family.
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Research into treatments for Spielmeyer-Vogt disease is ongoing due to its severity and early onset.
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Children diagnosed with Spielmeyer-Vogt disease often face severe challenges.
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Doctors diagnosed the child with Spielmeyer-Vogt disease after he began to lose his vision and cognitive abilities.
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Because Spielmeyer-Vogt disease is inherited, genetic counseling was recommended for the affected family.
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The symptoms of Spielmeyer-Vogt disease can appear as early as three years old.
Synonyms
A rare childhood disease passed from parents that causes gradual blindness, loss of thinking ability, and early death
Surface Forms
Morphology
Spielmeyer-Vogt + disease
This is an eponymous medical name: knowing 'disease' lets a learner infer it is some kind of illness, but the surname component 'Spielmeyer-Vogt' carries no lexical meaning that would reveal the specific nature, symptoms, or cause. Therefore a B1 learner would get a partial (disease) sense but would not be able to derive the full clinical meaning without prior exposure or specialist knowledge.
Etymology
Spielmeyer-Vogt disease is named after the two doctors, Spielmeyer and Vogt, who first described the condition in children. So the name refers to the rare 'inherited' illness that begins in childhood and causes loss of sight, thinking problems, and early death.