- aminoaciduria cataract
- capsular thickening occurring in aminoaciduria, homocystinuria, and oculocerebrorenal syndrome.
Medical dictionary. 2011.
Medical dictionary. 2011.
Cataract — For other uses, see Cataract (disambiguation). Cataract Classification and external resources Magnified view of cataract in human eye, seen on examination with a slit lamp using diffuse illumination … Wikipedia
syndrome — The aggregate of symptoms and signs associated with any morbid process, and constituting together the picture of the disease. SEE ALSO: disease. [G. s., a running together, tumultuous concourse; (in med.) a concurrence of symptoms, fr. syn,… … Medical dictionary
Galactosemia — A genetic metabolic disease in which there is a defect in the body s ability to use the sugar galactose. In classic galactosemia, the basic defect is a deficiency of the enzyme known as GALT (galactose 1 phosphate uridyl transferase). This causes … Medical dictionary
List of diseases (D) — A list of diseases in the English wikipedia.DiseasesTOC D* D ercole syndromeDa* Daentl Towsend Siegel syndrome * Dahlberg Borer Newcomer syndrome * Daish Hardman Lamont syndrome * Dandy Walker facial hemangioma * Dandy Walker malformation… … Wikipedia
List of diseases (A) — A listing of diseases.DiseasesTOC Aa Ab* Aagenaes syndrome * Aarskog Ose Pande syndrome * Aarskog syndrome * Aase Smith syndrome * Aase syndrome * ABCD syndrome * Abasia * Abdallat Davis Farrage syndrome * Abdominal aortic aneurysm * Abdominal… … Wikipedia
Deficiency, GALT — Lack of the enzyme called GALT (galactose 1 phosphate uridyl transferase) which causes the genetic metabolic disease galactosemia, one of the diseases in many newborn screening panels. The disease can be fatal, if undetected. If detected, it can… … Medical dictionary
GALT deficiency — Lack of the enzyme called GALT (galactose 1 phosphate uridyl transferase) which causes the genetic metabolic disease galactosemia, one of the diseases in many newborn screening panels. The disease can be fatal, if undetected. If detected, it can… … Medical dictionary
Bhaskar Jagannathan syndrome — is an extremely rare genetic disorder that is characterized by the constellation of features like arachnodactyly, aminoaciduria, congenital cataracts, cerebellar ataxia, and delayed developmental milestones. When the entity was initially reported … Wikipedia
Disease — Illness or sickness often characterized by typical patient problems (symptoms) and physical findings (signs). Disruption sequence: The events that occur when a fetus that is developing normally is subjected to a destructive agent such as the… … Medical dictionary