Noun
/ˌkreɪni.oʊˌmɛtəˈfɪziəl dɪsˈpleɪz.i.ə/
Craniometaphysial dysplasia is a rare genetic disorder characterized by abnormal growth and development of the cranial bones and the metaphysis (the region of long bones). This condition affects bone structure, often leading to deformities in the skull and sometimes resulting in a decrease in bone density.
It is a clinical term used primarily in medical contexts and is often encountered in written documents such as medical literature, research articles, and reports. The term is not commonly used in everyday conversation.
Дислазия краниометафизии может часто привести к различным краниальным деформациям у пораженных детей.
The diagnosis of craniometaphysial dysplasia was confirmed after the recommended genetic testing.
Диагноз дислазии краниометафизии был подтвержден после рекомендованного генетического тестирования.
Research on craniometaphysial dysplasia is crucial for understanding its genetic basis.
While "craniometaphysial dysplasia" is a highly specific medical term and does not typically appear in idiomatic expressions, its usage can be relevant when discussing related medical or genetic themes. Below are idioms that connect to concepts of health or medical conditions:
Иногда семьям приходится стиснуть зубы, сталкиваясь с реальностью дислазии краниометафизии.
On the mend: Recovering from an illness or injury.
После операции пациент с дислазией краниометафизии наконец-то идет на поправку.
Keep one's chin up: To remain positive and hopeful in difficult situations.
The term craniometaphysial is derived from the following components: - Crani(o): from Latin cranium, meaning 'skull'. - Meta: from Greek metaphysikos, meaning 'beyond' or 'after'. - Physial: from physiology, which refers to the origin or function of biological processes.
The term dysplasia originates from Greek dysplasis, meaning 'malformation' (from dys- meaning 'bad' or 'difficult' + plasis meaning 'formation').
Synonyms: - Craniosynostosis (related but different condition)
Antonyms: - Normal bone growth
This term is a niche medical vocabulary item and is primarily relevant in specific medical, genetic, or healthcare settings rather than in general usage.