Синдром Темтамі
ORPHA:1777· ICD-10 Q87.8· Temtamy syndrome
Визначення(English summary)
A very rare congenital genetic neurological disorder characterized by agenesis/hypoplasia of corpus callosum with developmental abnormalities, ocular disorders, and variable craniofacial and skeletal abnormalities.
- Поширеність
- <1 / 1 000 000
- Успадкування
- Autosomal recessive
- Вік початку
- Antenatal, Infancy, Neonatal