MPTRVT

Congenital adrenal hyperplasia (CAH) refers to a group of autosomal recessive disorders that impair cortisol biosynthesis. CAH represents a continuous phenotypic spectrum with over 95% of all cases caused by 21hydroxylase deficiency. CAH owing to 21hydroxylase deficiency is the most common cause of genital ambiguity in the newborn and is present in about 1 in 15000 live births worldwide

Biocard™ Rapid HIV 1 and 2 flow through assay kit on Flow through assay method for differential detection of HIV 1 & 2 antibodies along with a in built procedural control.All the accessories needed for the sampling and testing are included.Works on Serum/PlasmaResults can be obtained in 5 minutes

Cystic Fibrosis (CF) is an autosomal recessive disorder affecting the lungs, pancreas, intestine and liver. CF is the most common in Caucasians with an incidence rate 1:2500 newborns. CF is caused by mutation in the gene for the protein cystic fibrosis transmembrane conductance regulator (CTFR) [1,2]. Large-scale neonatal screening for CF is performed by indentification of increased levels of immunoreactive trypsinogen (IRT) in blood.

Labsystems Diagnostics Biocard M.pneumoniae IgM is a rapid test for the detection of IgM antibodies against Mycoplasma pneumoniae from serum fingertip blood or intravenous blood sample.