. http://www.chop.edu/conditions-diseases/sacrococcygeal-teratoma-sct/about#.VsTF7_krJhE. Accessed 1/22/2016. Do you know of a review article? We want to hear from you. You can help advance rare disease, : Rare Cancers Summary Summary Listen A sacrococcygeal teratoma is a tumor that grows at the base of the spine in a developing fetus. It occurs in one in 40,000 newborns and girls are four times more ...
) are not present at birth, but they begin to appear during childhood. People with severe MPS I develop the features of this condition earlier than those with attenuated MPS I. The following list includes, 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 articles that discuss ...
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 of medical, keratoderma type 1 See More Categories: Congenital and Genetic Diseases; Skin Diseases This disease is grouped under: Palmoplantar keratoderma Summary Summary Listen Punctate palmoplantar keratoderma type I is ...
More Categories: Congenital and Genetic Diseases; Metabolic disorders; Nervous System Diseases Summary Summary Listen Mitochondrial complex I deficiency is a type of mitochondrial disease. Mitochondria, . 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 ...
: Urethral duplication Categories: Congenital and Genetic Diseases; Kidney and Urinary Diseases Summary Summary Listen Duplication of urethra is a very rare condition where there is an extra urethra, instead, 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 is free of charge ...
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 of medical, Urinary Diseases; Skin Diseases See More Summary Summary Listen Swyer syndrome is a genetic condition affecting sexual organ development, classified as a disorder of sex development (DSD). In Swyer syndrome ...
portal for information on rare diseases and orphan drugs.Orpha Number: 73272DefinitionGrowth delay due to insulin-like growth factor I deficiency is characterised by the association of intrauterine and, researchers. OMIM is maintained by Johns 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 ...
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 articles that discuss, /article/1258678-overview. Mucopolysaccharidoses. NORD. 2011; http://rarediseases.org/rare-diseases/mucopolysaccharidoses/. Do you know of a review article? We want to hear from you. You can help advance ...
rare disease can impact the daily lives of patients and families. These resources can help families navigate various aspects of living with a rare disease. Financial Resources The Social Security, designed to make it easier to compare the signs and symptoms (phenotypes) of different diseases and discover common features. This initiative is a collaboration between several academic institutions across ...
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 articles that discuss Sialidosis, two types, which are distinguished by the age at which symptoms appear and the severity of features. Sialidosis type I is the less severe form of this condition. People with this condition typically ...
