What is Disease?
Disease, any harmful deviation from the
normal structural or functional state of an organism, generally associated with
certain signs and symptoms and differing in nature from physical injury. A
diseased organism commonly exhibits signs or symptoms indicative of its
abnormal state.
In other words it can also be defined as
A disease is a particular
abnormal condition that negatively affects the structure or function of all or
part of an organism, and that is not due to any immediate external injury.
Diseases are often known to be medical conditions that are associated with
specific signs and symptoms.
What are the 4 types of diseases?
There are four main types of disease:
1)
Infectious diseases
2) Deficiency diseases
3) Hereditary diseases (including both genetic diseases and
non-genetic hereditary diseases)
4)
Physiological diseases.
Infections can be brought about by numerous microorganisms, including Bacteria, Viruses, Fungi, and Parasites that might cause sickness and illness. For people, transmission of microbes might happen in an assortment of ways: spread from individual to-individual by direct contact, water or foodborne ailment or aerosolization of tainted particles in the climate and through crawlies (mosquitoes) and ticks.
Signs and symptoms and
treatment of infectious diseases depend on the host and the pathogen.
What are the symptoms of infectious diseases?
Symptoms of infectious disease are
particular to the type of disease. For example, symptoms of influenza include:
Other infectious diseases, such as
Shigella, cause more serious symptoms, including:
- Bloody diarrhea
- Vomiting
- Fever
- Dehydration (lack of fluid)
- Shock
You might go through one or a few indications of an irresistible infections. See a specialist on the off chance that you have any constant (progressing) indications or side effects that deteriorate your health over the long span of time.
Most Common Infectious Disease
Infectious diseases can be any of the following:
Chickenpox |
Pneumonia |
Diphtheria |
Rubella (German measles) |
Common cold |
Rocky mountain spotted fever |
E. coli |
Salmonella infections |
Giardiasis |
Severe acute respiratory syndrome (SARS) |
Infectious mononucleosis |
Shingles (herpes zoster) |
HIV/AIDS |
Sexually transmitted diseases |
Influenza (flu) |
Tetanus |
Lyme disease |
Toxic shock syndrome |
Measles |
Viral hepatitis |
Malaria |
Tuberculosis |
Meningitis |
West Nile virus |
Mumps |
Whooping cough (pertussis) |
Poliomyelitis (polio) |
|
Signs and symptoms of vitamin
deficiency include:
Fatigue |
Weight
loss |
|
Shortness
of breath |
Numbness
or tingling in your hands and feet |
|
Dizziness |
Muscle weakness |
|
Pale
or yellowish skin |
Personality changes |
|
Irregular
heartbeats |
Unsteady movements |
|
|
|
Mental confusion or forgetfulness |
Here is
the list of common deficiency diseases with their respective causes.
Deficiency |
Disease |
Calcium |
stypsis |
Rickets |
|
Tetany |
|
Iodine deficiency |
Goitre |
Selenium deficiency |
Keshan disease |
Iron deficiency |
Iron deficiency anaemia |
Zinc |
Growth retardation |
Thiamine (Vitamin B1) |
Beriberi |
|
|
Niacin (Vitamin B3) |
Pellagra |
Vitamin C |
Scurvy |
Vitamin D |
Steprsis |
Rickets |
|
Vitamin A |
Night Blindness |
Vitamin K |
Haemophilia |
An innate/hereditary sickness is regularly portrayed as something that "runs in the family." It is passed down from one or the two guardians to, a then kid pass it to their kids. Inherited infection is because of transformations of the hereditary material of cells. Such changes can happen at the level of a chromosome (chromosomal transformations), the (genome transformation), or a (quality transformations). Transformations change either the design or the measurements of one or a few qualities. Most, however not all, inherited sicknesses are independently uncommon (1), but rather taken together they include about 5% of the illness load in created nations.
Genetic
Disorders
What
are genetic disorders?
Genetic disorders is a category of
diseases that includes certain types of birth defects, chronic diseases, developmental problems, and sensory deficits that are inherited from one or
both parents.
Birth defects |
Chronic diseases |
Developmental
problems |
Sensory Deficits |
cataracts |
bleeding disorders |
autism spectrum disorders |
extreme farsightedness |
cleft lip or palate |
childhood cancers |
attention deficit/hyperactivity |
extreme nearsightedness |
congenital heart disease |
kidney or urinary tract disease |
developmental delay |
hearing loss |
contractures |
slow growth or short stature |
failure to thrive |
retinal or other visual problems |
diaphragmatic hernia |
cystic fibrosis |
learning disability |
|
genital malformations |
sickle cell disease |
loss of developmental skills |
|
glaucoma |
thalassemia |
low muscle tone |
|
misshapen skull |
|
mental illness |
|
missing fingers or toes |
|
mental retardation |
|
missing or incomplete arms or legs |
|
speech problems |
|
spina bifida or open spine defects |
|
seizures |
|
Similarities can be found in some of the symptoms that are not interested. Features can appear at birth (congenital heart disease
or cleft lip or palate) or during the course of childhood (developmental delays
or learning problems). Conclusion might be drawn from an actual test or designated hereditary testing
What
are the physical signs of genetic disorders?
The following list includes
features that might suggest that your child has a genetic disorder. In few cases, a portion of these attributes are normally found in individuals without any genetic problem. You'll need to check with your primary care physician if your child has something like two of the accompanying highlights::
ear abnormalities |
misshapen teeth |
unusually shaped eyes |
missing or extra teeth |
different colored eyes |
loose or stiff joints |
facial features that are unusual or different
from other family members |
unusually tall or short stature |
brittle or sparse hair |
webbed fingers or toes |
excessive body hair |
excessive skin |
white patches of hair |
unusual birthmarks |
large or small tongue |
increased or decreased sweating |
|
unusual body odor |
What Are the Types of Genetic Disease?
There
are many types of genetic diseases. Four of the main types are:
- Single-gene
inheritance diseases
- Multifactorial
genetic inheritance disorders
- Chromosome
abnormalities
- Mitochondrial
genetic inheritance disorders
List of Examples of Common Single-Inheritance Genetic Diseases
Single
gene inheritance diseases are diseases that occur because one defective gene . They are known as monogenetic disorders. There are thousands of known
single gene inheritance diseases, and they may be inherited in different ways.
Autosomal dominant inheritance means that only one copy of the defective gene
(from either parent) must be present to cause the condition. Autosomal
recessive diseases require that an affected person receive a defective copy of
the gene from each parent. X-linked disorders refer to diseases for which the
defective gene is present on the female (X) chromosome.
Examples of single gene inheritance disorders
include:
- Cystic fibrosis
- Sickle-cell anemia
- Marfan syndrome
- Duchenne muscular dystrophy
- Huntington disease
- Polycystic kidney disease types
1 and 2
- Tay-Sachs
disease Phenylketonuria
- Maple syrup urine disease
- Neurofibromatosis
type 1
- Alpha-1
antitrypsin deficiency
- Galactosemia
- Familial hypercholesterolemia
- Rett
syndrome
- Hemophilia
- Fanconi
anemia
- Kartagener
syndrome
- Xeroderma
pigmentosum
- Hereditary
spherocytosis
- Tuberous
sclerosis
- Von
Hippel-Lindau syndrome
List of Examples of Multifactorial Genetic Inheritance Disorders
- A
genetic disease or disorder is any disease caused by a problem with a
person’s genes. A person’s genes are contained within their genome. The
human genome is made up of the 46 human chromosomes (22 pairs of autosomal
chromosomes and 2 sex chromosomes). These 46 chromosomes together contain
over 3 billion base pairs of DNA that contain about 20,500 protein-coding
genes. The actual protein-coding genes account for less than 5% of the
human genome. The precise function of the 95% of remaining DNA is unclear.
Some researchers include mitochondrial DNA as part of the human genome.
- There
are about 6000 known genetic disorders; many are fatal or cause severe
problems while others may not but may add to problems that are triggered
by non-genetic (for example, environmental conditions).
- Genetic
disorders can range from a defect in a single base mutation in the DNA of
one gene to chromosomal abnormalities that involve deletion or addition of
entire chromosomes or sets of chromosomes. Genetic disorders can be
inherited, or passed from parents to offspring, or acquired due to changes
in an individual’s DNA that occur during their lifetime. Radiation and
certain cancer-causing chemicals are examples of
causes of acquired changes to DNA. This short article is designed to give
the reader a list of groups of diseases that share genetic problems that
are similar in cause. The lists have examples of genetic disease types and
are not all inclusive.
List of Examples of Chromosome Abnormalities Genetic Diseases
- Chromosome abnormalities usually result from a problem
with cell division and arise because of duplications or absences of entire
chromosomes or pieces of chromosomes. Examples of chromosome abnormality
disorders include:
- Down syndrome
- Cri-du-chat
syndrome
- Klinefelter
syndrome
- Patau
syndrome (trisomy 13)
- Edwards syndrome (trisomy 18)
- Turner
syndrome
- 22q11.2
deletion syndrome
- Ring
chromosome 14 syndrome
- Prader-Willi
syndrome
List of Examples of Mitochondrial Genetic Inheritance Disorders
Mitochondrial genetic inheritance disorders are
caused by mutations in the DNA of mitochondria, small particles within cells.
This DNA is unique in that it is not located on the chromosomes in the cell
nucleus. Mitochondrial DNA is always inherited from the female parent since egg
cells (unlike sperm cells) keep their mitochondrial DNA during the process of fertilization. Examples of mitochondrial
genetic inheritance disorders include:
- Hereditary
optic atrophy
- Barth
syndrome
- Co-enzyme
Q10 deficiency
- Myoclonic epilepsy with
ragged red fibers (MERRF)
- MELAS
syndrome, a rare form of dementia
- Kearns-Sayre
syndrome
- Pearson
syndrome
- Neuropathy,
ataxia, retinitis pigmentosa (NARP)
- Leigh’s
disease
Physiological diseases
A physiological
disorder is an illness that interferes with the way that the
functions of the. body are carried out. Examples are: Diabetes, Alzheimer's, Parkinson's,
rheumatoid arthritis, asthma, leukemia, coronary heart. disease, any form of
cancer.
A physiological disorder is a condition
in which the organs in the body malfunction causes illness. Examples are
Asthma, Glaucoma,
Diabetes.
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