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List of articles in "Disease" category - Page 345

MELAS syndrome

Mitochondrial encephalomyopathy lactic acidosis and stroke-like episodes – abbreviated to MELAS – is one of the family of mitochondrial cytopathies which also include MERRF and Leber’s hereditary optic neuropathy. It […]


Nijmegen breakage syndrome

Nijmegen breakage syndrome (NBS) also known as Berlin breakage syndrome and Seemanova syndrome is a rare autosomal recessive congenital disorder causing chromosomal instability probably as a result of a defect […]


Language disorder

Language disorders or language impairments are disorders that involve the processing of linguistic information. Problems that may be experienced can involve grammar (syntax and/or morphology) semantics (meaning) or other aspects […]


Secondary hyperparathyroidism

Secondary hyperparathyroidism refers to the excessive secretion of parathyroid hormone (PTH) by the parathyroid glands in response to hypocalcemia (low blood calcium levels) and associated hypertrophy of the glands. This […]


Adams–Oliver syndrome

Adams–Oliver syndrome (AOS) is a rare congenital disorder characterized by defects of the scalp and cranium (cutis aplasia congenita) transverse defects of the limbs and mottling of the skin.


Warfarin necrosis

Warfarin-induced skin necrosis (or more generally coumadin-induced skin necrosis or Anticoagulant-induced skin necrosis) is a condition in which skin and subcutaneous tissue necrosis (tissue death) occurs due to acquired protein […]


Activated protein C resistance

Activated protein C resistance (APCR) is a hemostatic disorder characterized by a poor anticoagulant response to activated protein C (APC). This results in an increased nathan of venous thrombosis which […]


Acrospiroma

An acrospiroma (also known as a clear cell hidradenoma dermal duct tumor hidroacanthoma simplex nodular hidradenoma and poroma) is a tumor of the distal portion of a sweat gland. Acrospiromas […]


Bernard–Soulier syndrome

Bernard–Soulier syndrome (BSS) also called hemorrhagiparous thrombocytic dystrophy is a rare autosomal recessive coagulopathy (bleeding disorder) that causes a deficiency of glycoprotein Ib (GpIb) the receptor for von Willebrand factor […]


Intrauterine hypoxia

Intrauterine hypoxia occurs when the fetus is deprived of an adequate supply of oxygen. It may be due to a variety of reasons such as prolapse or occlusion of the […]


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