National Institutes of Health. Visit the website to explore the biology of this condition. Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database, nevus; Verrucous epidermal nevus; Verrucous nevus; Inflammatory linear verrucous epidermal naevus; Inflammatory linear verrucous epidermal nevus See More Categories: Rare Cancers; Skin Diseases Subtypes ...
. Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge. PubMed is a searchable database of medical literature and lists journal, syndrome. Orphanet. March, 2015; http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=820. Wu S, Xu Z, Liang H. Sneddon’s syndrome: a comprehensive review of the literature. Orphanet J Rare Dis. 2014 ...
National Institutes of Health. Visit the website to explore the biology of this condition. Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database, /hematology-and-oncology/anemias-caused-by-hemolysis/hemoglobin-s-c-disease. Do you know of a review article? We want to hear from you. You can help advance rare disease research! You can help advance rare ...
cause is related to a rare non-cancerous tumor called a craniopharyngioma.[2][3] When this tumor is removed, the hypothalamus can get damaged leading to the symptoms of hypothalamic obesity. Other causes, for hypothalamic obesity include other rare tumors, head trauma, swelling in the brain and being born with a brain malformation.[2] Certain genetic syndromes also include symptoms of hypothalamic ...
Listen The following summary is from Orphanet, a European reference portal for information on rare diseases and orphan drugs.Orpha Number: 219DefinitionA subtype of autosomal recessive limb-girdle muscular, information on rare diseases and orphan drugs. Access to this database is free of charge. PubMed is a searchable database of medical literature and lists journal articles that discuss Limb-girdle muscular ...
rare diseases and the organizations that serve them. In-Depth Information GeneReviews provides current, expert-authored, peer-reviewed, full-text articles describing the application of genetic testing to, Hopkins University School of Medicine. Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge. PubMed is a searchable database ...
Epithelioid sarcoma Title Summary Summary Listen Epithelioid sarcoma (ES) is a rare cancerous tumor that most often occurs in the soft tissue of the fingers, hands and forearms of young adults. It, cancer has spread to other parts of the body.[1][2][3] Last updated: 5/7/2020 Symptoms Symptoms Listen The following list includes the most common signs and symptoms in people with epithelioid sarcoma (ES ...
factsheet on Limbic encephalitis with LGI1 antibodies In-Depth Information Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge, long-term outcome. Neurology. 2016 Aug 23; 87(8):759-65. Varley J, Taylor J, Irani SR. Autoantibody-mediated diseases of the CNS: Structure, dysfunction and therapy. Neuropharmacology. 2017:1-12 ...
Tumefactive multiple sclerosis Title Other Names: Diffuse cerebral sclerosis of Schilder; Concentric demyelination; Balo's concentric sclerosis; Diffuse cerebral sclerosis of Schilder; Concentric, demyelination; Balo's concentric sclerosis; Marburg variant; Balo disease; Baló concentric sclerosis; Balo's disease; Encephalitis periaxialis concentrica See More Categories: Nervous System Diseases ...
condition. Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge. PubMed is a searchable database of medical literature and lists, depend on the infection(s) present in each person. The cause of developing anti-interferon-gamma autoantibodies is unclear, but genetic factors are suspected to be involved.[2] Studies have suggested an ...
