Аутосомно-рецесивна вторинна поліцитемія, не повязана з геном VHL
ORPHA:247378· ICD-10 D75.1· Autosomal recessive secondary polycythemia not associated with VHL gene
Визначення(English summary)
A rare, hereditary, hematologic disease characterized by an increase in hemoglobin, hematocrit and erythrocyte mass resulting in plethora or ruddy complexion, headache, dizziness, tinnitus and exertional dyspnea. In some cases, thrombophlebitis and arthralgia have also been reported.
- Поширеність
- Unknown
- Успадкування
- Autosomal recessive
- Вік початку
- Infancy, Neonatal