
These diseases which remain confined to a person.They are neither present at birth nor spread from one person to another. The diseases are caused due to some specific factors. They may be caused due to improper functioning of an organ (shortsightedness, hypertension, arthritis), hormonal imbalance (diabetes, dwarfism), allergy, cancer, inadequate diet (anaemia, goitre), etc.
NON COMMUNICABLE DISEASES |
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Cause |
Name of Disease |
Symptoms |
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1. Protein Energy (PEM) |
Marasmus (infants below 1 year) |
Shrivelled appearance, thinning of limbs, prominent ribs, retarded physical and mental growth, digestive disorder, repeated diarrhoea. |
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2. Protein (PEM) |
Kwashiorkor |
Loss of appetite, stunted growth, bulging eyes, enlarged stomach, long thin and curved legs. |
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3.Iron |
Anaemia |
Become pale, loose appetite, feels tired |
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4.Vitamin B12 (Cyanocobalamine) |
Perirniciousanaemia |
Become pale, loose appetite, feels tired, reduced number of RBCs. |
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5. Folic acid |
Macrocytic anaemia |
Become pale, loose appetite, feels tired, reduced growth of RBCs. |
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6. Iodine |
Goitre |
Abnormal enlargment of thyriod swelling in the neck reduced thyriod function, retarded growth |
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7. Vitamin A (calciferol) |
Xeropthalmia |
Night blindness dryness of cornea |
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8. Vitamin D (calciferol) |
Rickets (children) osteomalacia (adults) |
Twisted, thin soft bent bones deformed ribs. |
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9. Vitamin B1 (Thiamine) |
Beri−beri |
Muscular dystrophy, nervous disorder |
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10. Vitamin B5 (Niacin) |
Pellagra |
4d syndrome (dermatitis, diarrhoea, dementia, death) |
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11. Vitamin −C (Ascorbic acid) |
Scurvy |
Bleeding gums, loosening and falling of teeth, loose of weight |
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12. Degeneration |
Heart attack, liver failure, kidney |
Hypertension, liver megaly etc. |
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13. Hyper sensitivity |
Allergy |
Sneezing, coughing,, watering of eyes, asthma have fever |
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14. Uncontrolled growth of cells |
Cancer and tumour |
Loss of weight, person becomes weak, can lead to death or destruction of affected organ |
Diseases that are transmitted from parents to offsprings are called hereditary or genetic diseases. Some genetic diseases are as follows:
(a) Haemophilia:It is a sex linked hereditary disease. The genes of the disease are found on sex chromosome −X. due to this disease blood clots very slow so patient can be die due to excess of haemorrhage. Due to presence of one normal X chromosomes, the disease is not developed in women generally. Women act as carrier only. While in man the recessive gene can be expressed, if present of a X−chromosome.
(b) Colourblindness: This is a sex linked hereditary disease, its genes are situated on X−chromosomes. In this disease also women are found as carrier generally and men as patients. A person suffering from colour blindness cannot differentiate between red and green colour.
(c) Thalesemia: It is a genetic disease that leads synthesis of defective haemoglobin. Blood of patient have to be changed frequently. Cause of this disease is a recessive gene.
(d) Sickle Cell Anaemia:Cause of this disease is a mutation in gene. In this disease shape of red blood cell becomes sickle like. A child with 50% sickle shaped red blood cells and 50% normal red blood cells can survive and remain anaemic.

