Laboratory

Tests We Offer General Laboratory services and the following 

chemistry 

AMYLASE, LIPASE

TROPONIN I, CKMB, LDH, MYOGLOBIN

C-REACTIVE PROTEIN

HBA1C

D-DIMER

HORMONAL PROFILE

Estrogen,Progesterone,Follicle-stimulating hormone (FSH),Testosterone/DHEA,Thyroid hormones,Luteinizing hormone,Prolactin,Cortisol, insulin,Growth Hormone,Adrenocorticotropic Hormone,Calcitonin,Catecholamines)

TUMOR MARKERS( PSA,AfP,CEA,CA125

THYROID FUNCTION TEST

FAECAL IMMUNOCHEMISTRY TEST 

MICROALBUMINURIA

FOLIC ACID

VITAMIN B12

VITAMIN D3

IRON STUDIES(Serum iron,Ferritin,Transferrin

Total iron-binding capacity (TIBC):,Transferrin saturation:)

LFT

kidney profile 

Lipid profile 

STD SCREENING ( HiV1&2, VDRL, HCV, HBSAg, HAV)

microbiology( MANTOUX)

Cytology 

LIQUID BASED CYTOLOGY

HPV SCREENING(pap smear)

Hematology 

FBC, Blood group, genotype 

DNA Test

paternity testing 

Prenatal DNA Test

ultrasound 

others

PRENATAL SCREENING TEST

Unity Test

UNITY test is a simple blood test that is safe, accurate and affordable for all pregnant women. The only cell-free DNA test that screens the baby’s risk for:

Cystic Fibrosis

Sickle Cell

Alpha Thalassemia

Spinal Muscular Atrophy.

We sequence small fragments of your baby’s DNA that made its way from the placenta into your bloodstream. The test is safe for you and your baby as blood is drawn from your arm.

The UNITY is the only test that screens mother and child for conditions like Cystic Fibrosis, Sickle Cell, Alpha Thalassemia and Spinal muscular Atrophy with a single tube of blood.

Using patented technology, only UNITY can assess your baby’s risk for recessively inherited conditions and your baby’s Rh type.

With the UNITY you can also screen your pregnancy for conditions like Down syndrome (Trisomy 21), Edward Syndrome (Trisomy 18), Patau Syndrome (Trisomy 13) and gender of your baby if you chose to know. The UNITY has a 98 % accuracy for chromosomal abnormalities screening.

Nifty Test

The NIFTY test is a non-invasive prenatal test (commonly termed an NIPT) that screens for Down syndrome and certain other genetic conditions caused by extra or missing genetic information in the baby’s DNA. It’s important to note that all NIPTs like NIFTY, are screening tests and are not classified as diagnostic. This means that they are not 100% accurate and that ‘false positive’ or ‘false negative’ results can very rarely occur.

NIFTY consists of a small maternal blood draw and is available from as early as week 10 of pregnancy. Results are available within 10 working days.

NIFTY offers higher rates of accuracy than traditional screening tests and, unlike invasive procedures such as amniocentesis, poses no miscarriage risk to the mother or baby.

NIFTY screens for the three most common trisomy conditions present at birth which are Down syndrome, Edwards Syndrome and Patau Syndrome