How to book a Baby Shield TMS 62 Test (LC) at home near me?

You can easily book a Baby Shield TMS 62 Test (LC) in Parel, Mumbai with Max Lab by Max Hospitals. Just follow these simple steps:

Search for Baby Shield TMS 62 Test (LC) near me on Google and click on the result with the Max Lab Website. OR Download the Max Lab App from Google Play Store or App Store.

Select Baby Shield TMS 62 Test (LC) from the "Book a test" button or search from the search bar on the website or Max Lab App.

Add other tests that you want to include with Baby Shield TMS 62 Test (LC) for home collection in Parel, Mumbai.

Choose a convenient date and time slot for sample collection.

A trained and certified phlebotomist will visit your preferred location — home or office — at the scheduled time to collect your blood sample safely.

You can also track your order at each step and view its status.

The sample will be processed at the nearest Max Hospital or Max Laboratory, and your test reports will be delivered within the specified time.

Track your health and past records with Max Lab's special feature that allows you to compare results with previous reports.

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I received my reports via SMS and email within 24 hours. Logging in with OTP was seamless, and the report format was easy to understand. Very efficient!

Vansh

The technician arrived right on time. The entire process felt clean and safe. Ideal for anyone who prefers testing from home!

Swayam

Booked a full-body checkup through the Max Lab website in less than 2 minutes. Loved how I could select my city and get location-specific pricing. Super convenient!

Test Name :	Baby Shield TMS 62 Test (LC)
Also Known as :	Tandem Mass Spectrometer, TMS Blood Test, Newborn Screening, Newborn Screening Test
Sample Type :	Blood
Gender :	Both
Age group :	All Age Groups
This Test Includes :	Congential Hypothyroidism G6PD Deficiency (G6PD) Biotinidase deficiency Congenital Adrenal Hyperplasia (17-OHP) Congenital Hypothyroidism (TSH) Cystic Fibrosis Galactosemia Sickle Cell Anaemia (Hb SS) Beta thalassemia Sickle Cell Disease Variant hemoglobinopathies(C.D,H, bart band) including Hb E(Var Hb) Amino acid Disorders Argininemia ARG Argininosuccinic aciduria 5-oxoprolinuria carbamoyl phosphate synthetase 1- deficiency Citrullinenia CIT-I Homocystinuria Hypermethioninemia Hyperornithinemia-hyperammoninemia-hyperhomocitrullinemia (HHH) syndrome Hyperornithinemia with Gyral Atrophy 1 HOGA Maple syrup urine disease (MSUD) Classical Hyperphenylalaninemia Transient neonatal tyrosinemia Tyrosinemia Type 1 Tyrosinemia Type II Tyrosinemia Type III Ornithine transcarbamylase deficiency Citrullinemia type II Biopterin defect in cofactor biosynthesis BIOPT (BS) Bioptrin defect in confactor regeneration BIOPT (REG) Fatty Acid Oxidation and Other Disorders Carnitine Acylcarnitine Translocase Deficiency CACT 3-Hydroxy Long Chain Acyl-CoA Dehydrogenase Deficiency LCHAD Medium chain acyl CoA dehydrogenase deficiency Neonatal Carnitine Palmitoyl Transferase Deficiency Type II CPT-II Very Long Chain Acyl-CoA Dehydrogenase Deficiency VLCAD Carnitine Palnitoyl Transferase Deficiency Type II CPT-I 2,4-Dienoyl-CoA Reductase Deficiencyl DE-RED Multiple Acyl-CoA Dehydrogenase Deficeincy GA-II Short chain acyl CoA dehydrogenase deficiency Trifunctional Protein Deficiency TFP Short chain Hydroxy Acyl-CoA Dehydrogenase Deficiency SCHAD 3-Hydroxy-3-Methylglutary-CoA Lyase Deficiency HMG Gluatric Acidemia Type 1 GA-1 Isobutyryl-CoA dehydrogenase deficiency (IBD) Isovaleric acidemia 2-Methylbutyryl-CoA Dehydrogenase Deficiency 2MBG 3-Methylcrotonyl-CoA Carboxylase Deficiency 3MCC 3-Methylglutaconyl-CoA Hydratase Deficiency 3MGA Methymalonyl-CoA Mutase Deficiency MUT Maternal Vitamin B12 Deficiency Mitochondrial Acetoacetyl-CoA Thiolase Deficiency BKT Propionic acidemia Multiple CoA Carboxylase Deficiency MCD Malonic acidemia (MAL) Hyperalimentation Medium Chain Triglyceride Oil Administration MCT Treatment with benzoate, Pyvalic Acid, or Valproic Acid Liver Disease Presence of EDTA Coagulants in Blood Specimen Carnitine Uptake Deficiency CUD Medium-chain ketoacyl-CoA thiolase deficiency MCAT Methylmalonic Acidemia ( Cobalamin disorders) Cbl A, B Methylmalonic Acidemia with homocystinuria Cbl C, D 65 Tests

Price :	₹ 6750
Home Sample Collection Available

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Baby Shield TMS 62 Test (LC) Price in Parel, Mumbai

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BABY SHIELD TMS 62 TEST SAMPLE REPORT

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How to book a Baby Shield TMS 62 Test (LC) at home near me?

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