Directory
Hematuria syndrome with lumbar pain
Hematuria syndrome with low back pain is a complex of symptoms characterized by the appearance of blood in the urine (hematuria) on the f...
Lateral meningocele syndrome
Lateral meningocele syndrome is a rare congenital disorder characterized by herniation of the dura mater...
Levator syndrome
Levator syndrome is a complex neurological disorder characterized by abnormal contraction of the levator muscles...
Lethal congenital contracture syndrome
Lethal Congenital Contracture Syndrome (LCCS) is an extremely rare autosomal recurrent...
Lymphedema-distichiasis syndrome
Lymphedema-distichiasis syndrome is a rare genetic disorder characterized by a combination of congenital lymphedema of the lower...
Linear Nevus Sebaceous Syndrome
Linear nevus sebaceous syndrome is a rare congenital disorder characterized by the presence of linear skin lesions...
Linear hamartoma syndrome
Linear hamartoma syndrome is a rare dermatological disorder characterized by the presence of linear skin lesions...
Lenz microphthalmia syndrome
Lenz microphthalmia syndrome is a rare genetic disorder characterized by a complex of congenital anomalies in the development of the...
Long QT syndrome
Long QT syndrome is a hereditary or acquired disorder characterized by abnormal prolongation of the QT interval.
Long QT syndrome 1
Long QT syndrome is a hereditary or acquired cardiovascular disease characterized by...
Long QT syndrome 2
Long QT syndrome 2 (LQT2) is an inherited disorder characterized by abnormal prolongation of the inter...
Long QT syndrome 3
Long QT syndrome type 3 (LQT3) is an inherited disorder of myocardial repolarization characterized by a...
Long QT syndrome 5
Long QT syndrome (LQTS) is a hereditary or acquired disorder characterized by abnormal...
Lichen sclerosus
Lichen sclerosus (lichen sclerosus) is a chronic inflammatory skin disease characterized by impaired...
Nodules in the lungs
Lung nodules, also known as pulmonary nodules, are localized growths in the lung tissue that may be...
Lump in the abdomen
A lump in the abdomen is a clinical manifestation that may indicate various pathologies, including tumors,...
leukodystrophy
Leukodystrophy is a group of hereditary diseases associated with impaired myelination of nerve fibers. These diseases...
leukoplakia
Leukoplakia is a chronic disease characterized by excessive growth of squamous epithelium of the mucous membrane, most often the oral cavity...
leukocytosis
Leukocytosis is a condition characterized by an increase in the level of leukocytes (white blood cells) in the blood. This phenomenon usually occurs with...
listeriosis
Listeriosis is an infectious disease caused by the bacterium Listeria monocytogenes. This gram-negative bacterium belongs to the family...
MPI-CDG
MPI-CDG (angiopathy), also known as MPI-civil disgroupation, is a rare genetic disorder related to...
Mittelschmerz
Mittelschmerz, or mid-term pain, is a phenomenon that occurs in women during ovulation, when the egg is released...
Meige's disease
Meige's disease, or osteomalaxia, is characterized by a metabolic disorder in bone tissue, which leads to its softening and increased...
Antenatal exposure to methimazole
Methimazole is an antihyperthyroid drug used to treat hyperthyroidism, particularly Graves' disease. The drug reduces ...
Mitral valve atresia
Mitral atresia is a rare congenital heart defect in which the mitral valve is either absent or anatomically defective.
Muscle atrophy
Muscle atrophy is a pathological process characterized by a decrease in the volume of muscle tissue, which can lead to weakness, decreased...
Middle East Respiratory Syndrome (MERS)
Middle East respiratory syndrome (MERS) is an acute viral disease caused by the MERS-CoV coronavirus. The disease is charac...
Marchiafava Bignami disease
Marchiafava Bignami disease (or beta-thalassemia) is an inherited disorder characterized by a defect in the synthesis of protein...
Menetrier's disease
Menetrier's disease (or Menetrier's disease) is a rare but serious disorder of the stomach characterized by hypertrophy of the gastric mucosa...
Menkes disease
Menkes disease, or Menkes syndrome, is a rare inherited disorder characterized by a disorder of copper metabolism in...
