Here you can look through thousands of and diseases, ailments, medical conditions and illnesses. You can find the symptoms. Read about any ailment's diagnosis and find medications that can be used and the correct treatments that are needed.
Diseases, Illnesses & Ailments Starting from Letter M
- Marfan Syndrome
Marfan syndrome is a connective tissue disorder affecting many structures like skeleton, lungs, eyes, blood vessels and heart since connective tissue is found in all parts of the body. It is an inheritable condition in an autosomal dominant genetic pattern. [read more] - Marinesco-Sjogren Syndrome
Marinesco-Sjogren syndrome is a rare autosomal recessive disorder, which causes the destruction of the exocrine glands that is responsible for tear and saliva production. [read more] - Maroteaux-Lamy Syndrome
Maroteaux-Lamy syndrome is a rare disorder of mucopolysaccharide metabolism due to a deficiency of the enzyme aryl sulphatase B, the enzyme necessary to break down the complex sugar glycosaminoglycan (formerly referred to as mucopolysaccharide). This complex sugar needs to be recycled and replayed to carry out its normal function of providing structure to skin, bones, organs, and airways. It belongs to a group of uncommon inherited diseases categorized as lysosomal storage disorders. Other names for Maroteaux-Lamy syndrome are mucolopolysaccharidosis VI and MPS VI. [read more] - Marshall Syndrome
Marshall syndrome is a rare genetic disorder that is usually inherited in an autosomal dominant pattern. The condition can occur in both male and female. [read more] - Marshall-Smith Syndrome
Marshall-Smith syndrome is a rare genetic disorder involving specific facial features, remarkable accelerated skeletal maturation, failure to grow and thrive, and breathing problems that are severe in nature. [read more] - Martin Bell Syndrome
Martin Bell syndrome, also known as fragile syndrome X, is a mental defect that involves learning disabilities and behavioral problems. [read more] - Masculinisation
Masculinisation is a condition in which an affected female takes on a distinctly and progressively male appearance. [read more] - Mast Cell disease
Mast cell disease or mastocytosis is a group of rare disorders marked by the presence of too many mast cells in various organs and tissues such as the skin, spleen, liver, bone, and the gastrointestinal tract. [read more] - Mastalgia
Mastalgia is breast pain and is generally classified as either cyclical (linked with menstrual periods) or noncyclic. [read more] - Mastitis
Mastitis is a disease commonly seen in women breastfeeding refers to that kind of infection of the tissue surrounding the breast area which thereby results into the breast's painful swelling usually accompanied by its redness and tenderness. Most often, person affected with this infection are mothers who are breastfeeding their infants inasmuch as it occurs within the first six weeks after giving birth. However, even if the mother is affected with Mastitis, she can still breastfeed her child but usually feels tired and restless thereafter.` [read more] - Mastocytosis
Mastocytosis is a disorder that results when too many mast cells, called mastocytes, and CD34+ mast cell precursors exist in the body. It has many types and may be experienced by children and adults. [read more] - Mastocytosis
Mastocytosis is a group of unusual disorder of both children and adults caused by the presence of too many mast cells (mastocytes) and CD34+ mast cell precursors in a person's body. [read more] - Mastoiditis
By definition, Mastoiditis is an infection of the mastoid process, which is that part of the temporal bone of the skull and is located behind the ear. [read more] - MAT Deficiency
MAT deficiency is used to describe two metabolic disorders, which are unrelated -- Beta-ketothiolase deficiency and Hypermethioninemia. Beta-ketothiolase deficiency prevents the body from properly processing the products of lipid breakdown, known as amino acid isoleucine. Hypermethioninemia is a condition of excessive unprocessed amino acid methionine in the blood. [read more] - Maternal Death
Maternal death pertains to the death of a woman during or shortly after pregnancy that arises from factors or circumstances related to pregnancy or childbirth. It is also referred to as obstetrical death or maternal mortality. [read more] - Maturity Onset Diabetes of The Young
Maturity onset diabetes of the young is a condition in which the body has defective insulin but does not include any forms of type 2 diabetes. [read more] - McArdle disease
By definition MacArdle's disease is also known as Glycogen storage disease type V and is a kind of metabolic disorder that is characterized by the body's inability to produce enough of the muscle isoform called phosphorylase. Relatively recent, it was first identified in 1951 by the English physician whose name it now bears. [read more] - McCune-Albright Syndrome
McCune-Albright syndrome is also known as polyostotic fibrous dysplasia. It is a genetic condition with disorder of the bones, pigmentation of skin, and premature puberty with hormonal problems. [read more] - Measles
2Measles, which is also known as, Rubeola is a viral disease that has had a long history with medical accounts of it going as far back as 600 B.C. It was first clinically described in an Arabic book which significantly distinguished it from small pox. Measles is one of the great childhood killers, claiming the lives of more then 200 million children and adults in the last 150 years. The development of a vaccine has made the effectively checked the disease. [read more] - Meckel syndrome
By definition Meckel syndrome is also known as Meckel-Gruber Syndrome, Gruber Syndrome, Dysencephalia Splanchnocystica and is an extremely rare and often lethal genetic disorder; it is so rare that estimates for rates of incidence is about .02 for every 10,000 births. The country of Finland has the most number of cases with the incidence as high as 1.1 per 10,000 births. [read more]
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