Prolymphocytic leukemia is divided into two types according to the kind of cell involved: B-cell prolymphocytic leukemia and T-cell prolymphocytic leukemia. It is usually classified as a kind of chronic […]
List of articles in "Disease" category - Page 211
Anterior compartment syndrome of the lower leg
A compartment syndrome is an increased pressure within a muscular compartment that compromises the circulation to the muscles.
Medullary sponge kidney
Medullary Sponge Kidney (also known as Cacchi–Ricci disease) is a congenital disorder of the kidneys characterized by cystic dilatation of the collecting tubules in one or both kidneys. Individuals with […]
Pellucid marginal degeneration
Pellucid marginal degeneration (PMD; keratotorus) is a degenerative corneal condition often confused with keratoconus. It is typically characterized by a clear bilateral thinning (ectasia) in the inferior and peripheral region […]
Buschke–Ollendorff syndrome
Buschke–Ollendorff syndrome also known as Dermatofibrosis lenticularis disseminata is a rare genetic disorder associated with LEMD3. It is believed to be inherited in an autosomal dominant manner.It is named for […]
Paroxysmal extreme pain disorder
Paroxysmal extreme pain disorder (PEPD) originally named familial rectal pain syndrome is a rare disorder whose most notable features are pain in the mandibular ocular and rectal areas as well […]
Left posterior fascicular block
A left posterior fascicular block (LPFB) is a condition where the left posterior fascicle which travels to the inferior and posterior portion of the left ventricle does not conduct the […]
Left anterior fascicular block
Left anterior fascicular block is a cardiac condition distinguished from left bundle branch block.It is caused by only the anterior half of the left bundle branch being defective. It is […]
Sinoatrial block
The initial impulse in a heart is usually formed in the Sinoatrial (SA) node and carried through the atria down the internodal atrial pathways and to the Atrioventricular (AV) node. […]
Rothmund–Thomson syndrome
Rothmund–Thomson syndrome (RTS) also known as poikiloderma atrophicans with cataract or poikiloderma congenitale is a rare autosomal recessive skin condition originally described by August von Rothmund (1830–1906) in 1868. Matthew […]