Blindness

Axenfeld-Rieger syndrome is an autosomal dominant disorder of morphogenesis that results in abnormal development of the anterior segment of the eye, and results in blindness from glaucoma in approximately 50% of affected individuals. Systemic anomalies are associated, including dental hypoplasia, failure of involution of periumbilical skin, and maxillary hypoplasia.

Test Details
Description:
Delivery Time:
20 days
Sample:
2-5 Ml Venous Blood Sample / DNA sample
Alternative:

Test Details
Description:
Delivery Time:
20 days
Sample:
2-5 Ml Venous Blood Sample / DNA sample
Alternative:

Test Details
Description:
In vitro nucleic acid amplification test for qualitative detection of viral DNA in the clinical material using PCR.
Delivery Time:
Понеделник
Sample:
Blood sample (EDTA) / Throat swab
Alternative:
Cervical swab in case of CMV inf.

Leber hereditary optic neuropathy (LHON) is an inherited form of vision loss. Although this condition usually begins in a person's teens or twenties, rare cases may appear in early childhood or later in adulthood. For unknown reasons, males are affected much more often than females.

Test Details
Description:
Delivery Time:
30 days
Sample:
2-5 Ml Blood Sample / DNA sample
Alternative: