Hand-Schuller-Christian disease
- noun
- /hænd ˈʃʊlər ˈkrɪsʧən dɪˈziːz/
- Archaic
- Despite its rarity, Hand-Schuller-Christian disease should be considered in children with unexplained diabetes insipidus and bone lesions.
Examples
-
The pediatrician suspected Hand-Schuller-Christian disease when the child presented with multiple skull lesions and excessive thirst.
-
Diagnosis of Hand-Schuller-Christian disease requires clinical correlation and specific radiological findings.
-
What is Hand-Schuller-Christian disease?
-
The doctor diagnosed her with Hand-Schuller-Christian disease.
-
A child diagnosed with Hand-Schuller-Christian disease often shows symptoms like excessive thirst and skull lesions.
-
The symptoms of Hand-Schuller-Christian disease can include abnormal cholesterol metabolism and cranial bone defects.
-
To confirm Hand-Schuller-Christian disease, doctors look for specific clinical signs alongside imaging studies.
Synonyms
A rare disease mainly in young children that causes swelling, holes in the skull, and sometimes extreme thirst and urination
Surface Forms
Morphology
Hand-Schuller-Christian + disease
This is an eponymic name: a B1 learner who knows 'disease' would understand that it refers to an illness, but the sequence 'Hand‑Schuller‑Christian' are proper names with no semantic contribution to the specific medical features. Because the form signals the general category (disease) but provides no predictable information about symptoms or etiology, it is partially but not fully transparent.
Etymology
Hand-Schuller-Christian disease is named after three doctors, Hand, Schuller, and Christian, who first described the illness in 'children'. So the long name is just a label for a rare disease that can make small holes in the skull bones and cause very strong thirst.