
Bone Marrow Failure Syndrome Gene Panel







The Bone Marrow Failure Syndrome Gene Panel is a customized genetic test that analyzes a specific set of genes associated with bone marrow failure syndromes, a group of genetic disorders characterized by the inability of the bone marrow to produce an adequate number of blood cells. This panel consists of genes that are involved in various bone marrow failure syndromes, such as Fanconi anemia, Diamond-Blackfan anemia, Shwachman-Diamond syndrome, etc. It aims to identify specific genetic mutations or variations that may underlie the development of bone marrow failure. This information helps in accurate diagnosis and aids in formulating personalized treatment strategies for individuals affected by bone marrow failure syndromes. Furthermore, this panel helps uncover the genetic basis of these disorders, allowing a better understanding of the disease, thereby improving patient care.
Note: Genetic counseling can be provided. If interested, please send the request to this email id: [email protected]










Other tests
- CBC (Complete Blood Count)
- FBS (Fasting Blood Sugar)
- Thyroid Profile Total (T3, T4 & TSH)
- HbA1c (Glycosylated Hemoglobin)
- PPBS (Postprandial Blood Sugar)
- Lipid Profile
- Vitamin D (25-Hydroxy)
- Urine R/M (Urine Routine & Microscopy)
- Coronavirus Covid -19 test- RT PCR
- LFT (Liver Function Test)
- KFT (Kidney Function Test)
- TSH (Thyroid Stimulating Hormone) Ultrasensitive
- ESR (Erythrocyte Sedimentation Rate)
- Uric Acid, Serum
- Vitamin B12
- CRP (C-Reactive Protein), Quantitative
- Urine C/S (Urine Culture and Sensitivity)
- Serum Electrolytes
- Serum Calcium
- Serum Creatinine
- Diabetes Screening (HbA1C & Fasting Sugar)
- KFT with Electrolytes (Kidney Function Test with Electrolytes)
- Cholesterol - Total
- Hb (Hemoglobin)
- Complete Hemogram (CBC & ESR)















