Which of the following is not a hereditary disease?

By: Prof. Dr. Fazal Rehman | Last updated: February 3, 2024

QUESTION: Which of the following is not a hereditary disease? A Thalassemia B   Color-Blindness C   Haemophilia D    Leukemia ANSWER:       Leukemia  
Name of disease Genetic Cause Inheritance Pattern          Symptoms Treatment
Thalassemia Mutations in HBB or other genes Autosomal Recessive ·        Anemia ·        Fatigue ·        Potential organ damage. ·        Blood transfusions ·        Iron chelation ·        Bone marrow transplant
Cystic Fibrosis Mutations in CFTR gene Autosomal Recessive ·        Lung and digestive system problems ·        Increased mucus production. ·        Medications, ·        Airway clearance techniques ·        Lung transplant
Color Blindness Various gene mutations X-Linked Recessive ·        Difficulty distinguishing between certain colors, often red and green. ·        Color-correcting aids
Huntington’s Disease Mutations in HTT gene Autosomal Dominant ·        Progressive motor and cognitive deterioration. ·        Symptomatic treatment ·        Counseling ·        Support
Sickle Cell Anemia Mutations in HBB gene Autosomal Recessive ·        Abnormal red blood cells ·        Anemia ·        Organ damage ·        Blood transfusions ·        Pain management
Hemophilia Mutations in F8 or F9 genes X-Linked Recessive ·        Impaired blood clotting ·        Replacement clotting factor therapy
Duchenne Muscular Dystrophy Mutations in DMD gene X-Linked Recessive ·        Progressive muscle weakness ·        Loss of mobility ·        Physical therapy ·        Steroids ·        Supportive care
Tay-Sachs Disease Mutations in HEXA gene Autosomal Recessive ·        Neurodegeneration developmental delays ·        Supportive care and  symptom management.
Marfan Syndrome Mutations in FBN1 gene Autosomal Dominant ·        Tall stature ·        Heart and eye problems ·        Medications (beta-blockers) ·        Surgery (aortic repair)
Down Syndrome Extra copy of chromosome 21 Trisomy 21 ·        Intellectual disability ·        Distinctive physical features ·        Early intervention therapy
Polycystic Kidney Disease (PKD) Mutations in PKD1 or PKD2 genes Autosomal Dominant ·        Kidney cysts ·        Potential kidney failure ·        Symptomatic treatment ·        Dialysis ·        Kidney transplant
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