Синдром мікроделеції Xq21
ORPHA:1435· ICD-10 Q93.5· Xq21 microdeletion syndrome
Визначення(English summary)
An X-linked retinal dystrophy characterized by choroideremia, causing in affected males progressive nyctalopia and eventual central blindness. Obesity, moderate intellectual disability and congenital mixed (sensorineural and conductive) deafness are also observed. Female carriers show typical retinal changes indicative of the choroideremia carrier state.
- Поширеність
- <1 / 1 000 000
- Успадкування
- X-linked recessive
- Вік початку
- Infancy, Neonatal