Review Article

Parkinson’s Disease in Central Asian and Transcaucasian Countries: A Review of Epidemiology, Genetics, Clinical Characteristics, and Access to Care

Table 2

PD genetic studies in Central Asian countries.

nGenetic mutations studiedAnalysis methodResultsSample sizeCountry (reference)

1SNCA gene (Ala30Pro, Ala53Thr, Gly46Lis, Gly51Asp)PCR, gel electrophoresisNo pathogenic mutations found34 PD casesKazakhstan [6]
2GIGYF2PCR, Sanger sequencingNo pathogenic mutations foundNot statedKazakhstan [14]
3SNCA (Ala53Thr), Parkin (T240M), LRRK2 (G2019S), Nat2, GSTT1, and GSTM1PCR, Sanger sequencingG2019S was found in 5.7% of idiopathic PD and 17.6% of familial PD patients153 PD cases, 80 controlsUzbekistan [15]
4SNCA, ParkinNot stated13 (19.4%) positive to SNCA gene mutation, 27 (40.3%) positive to Parkin mutation67Uzbekistan [16]

PCR, polymerase chain reaction; PD, Parkinson’s disease.