PCR BASED DIAGNOSIS OF 21-HYDROXYLASE GENE DEFECTS IN SLOVAK PATIENTS WITH CONGENITAL ADRENAL HYPERPLASIA

Objective. To analyse 21-hydroxylase gene for 8 most common mutations in patients with saltwasting type of congenital adrenal hyperplasia. Methods. Allele specific PCR performed on 8 salt-wasting CAH patients and their 23 healthy relatives. Results. Two patients were homozygous for 8 bp deletion in exon 3, while 6 patients were homozygous for intron 2 splice mutation. Mutant allele for splice mutation was find also in both parents of patients with this type of mutation. Conclusions. These preliminary results show that only two mutations, 8 bp deletion in exon 3 and splice mutation in intron 2, were present in this group of Slovak patients with salt-wasting type of congenital adrenal hyperplasia.