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List of articles in "Disease" category - Page 35

Median nerve palsy

Injuries to the arm forearm or wrist area can lead to various nerve disorders. One such disorder is median nerve palsy. If the median nerve is damaged the ability to […]


Nipple adenoma

A nipple adenoma is a rare benign tumour of the breast.The condition may also be known as :Florid papillomatosis of the nippleFlorid adenomatosisSubareolar duct papillomatosisErosive adenomatosis↑


Hereditary mucoepithelial dysplasia

Hereditary mucoepithelial dysplasia (HMD) or simply mucoepithelial dysplasia is a rare autosomal dominant multiepithelial disorder causing systemic maldevelopment of the epithelia and mucus membranes that line the surface of tissues […]


Perlman syndrome

Perlman syndrome (PS) (also called renal hamartomas nephroblastomatosis and fetal gigantism) is a rare overgrowth disorder present at birth. It is characterized by polyhydramnios and fetal overgrowth including macrocephaly neonatal […]


Irregular sleep–wake rhythm

Irregular sleep–wake rhythm is a rare form of circadian rhythm sleep disorder. It is characterized by numerous naps throughout the 24-hour period no main nighttime sleep episode and irregularity from […]


22q11.2 duplication syndrome

22q11.2 duplication syndrome is a rare genetic disorder caused by a duplication of a segment at the end of chromosome 22.


ACR score for rheumatoid arthritis

ACR score is a scale to measure change in rheumatoid arthritis symptoms. It is named after the American College of Rheumatology.Different degrees of improvement are referred to as ACR20 ACR50 […]


Progressive transformation of germinal centres

Progressive transformation of germinal centres abbreviated PTGCs and also progressive transformation of germinal centers is a reactive lymph node process of undetermined etiology.


Renpenning’s syndrome

Renpenning’s syndrome is a neurodevelopmental disorder recognised in males that causes intellectual disability mild growth retardation with examples in the testes and head and a somewhat short stature. The condition […]


2q37 monosomy

2q37 monosomy is a rare genetic disorder caused by a deletion of a segment at the end of chromosome 2.


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