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List of articles in "Disease" category - Page 211

Prolymphocytic leukemia

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 […]


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 […]


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