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 […]
List of articles in "Disease" category - Page 35
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.