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Detailed Information on Muscular Dystrophy
Muscular dystrophy (MD) is a inherited disorder that slowly weakens the body's muscles. It's caused by inaccurate or missing genetic information that prevents the body from making the proteins it needs to build and maintain healthy muscles. There are... Detailed Information on Myopathy
Myopathy is a skeletal muscle disease or neuromuscular disorder. Myopathy can be obtained or inherited, and can arise at birth or later in life. Myopathies can cause from endocrine disorders, metabolic disorders, muscle infection or inflammation, dru... Detailed Information on Myelodysplastic Syndromes
Myelodysplastic syndrome (MDS) refers to a heterogeneous group of closely linked clonal hematopoietic disorders. Myelodysplastic syndromes (MDS) are a group of diseases that involve the bone marrow and blood. The bone marrow in myelodysplastic syndro... Detailed Information on Munchausen By Proxy Syndrome
Munchausen syndrome by proxy (MSBP) is a form of child abuse in which a parent induces real or apparent symptoms of a disease in a child. The caregiver almost always is a mother, and the victim, her child. Because children are the victims, MSBP is co... Detailed Information on Moyamoya Disease
Moyamoya illness is a rare, advanced cerebrovascular disorder characterized by the narrowing or occlusion of main blood vessels leading into the brain, and the formation of abnormal blood vessels called moyamoya vessels. It can occur at any time, but... Detailed Information on Mitral Valve Prolapse
Mitral valve prolapse is also known as click-murmur syndrome. Mitral valve prolapse (MVP) is a common heart disorder. Mitral valve prolapse is a common condition occurring in approximately 4 - 18% of the population. It comes when the valve between yo... Detailed Information on Mitochondrial Disease
Mitochondrial myopathies are a group of neuromuscular diseases. Mitochondrial diseases result from failures of the mitochondria, specialized compartments present in every cell of the body except red blood cells. The mitochondria alter the energy of f... Detailed Information on Methylmalonic Aciduria
Methylmalonic acidemia (MMA), also called methylmalonic aciduria. Methylmalonic Aciduria is a disorder of amino acid metabolism, involving a defect in the conversion of methylmalonyl-coenzyme A (CoA) to succinyl-CoA. This condition occurs in an estim... Detailed Information on Metachromatic Leukodystrophy
Metachromatic leukodystrophy (MLD) is known as the leukodystrophies. Metachromatic leukodystrophy (MLD) is a inherited disorder that affects nerves, muscles, and other organs. It slowly gets worse over time. Metachromatic leukodystrophy is reported t... Detailed Information on Microtia
Microtia is an abnormally small external ear (auricle). It can be unilateral (one side only) or bilateral (affecting both sides). Microtia is thought to be a “non-inducible” type of congenital malformation, which means that it is not typically the re...
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