| Health / Medical Topics |
Jervell and Lange Nielsen Syndrome
An autosomal recessive inherited syndrome caused by mutations in the KCNE1 and KCNQ1 genes. It is characterized by congenital hearing loss and arrhythmia. It is a form of long QT syndrome. (NCI Thesaurus)
YOU MAY ALSO LIKE
A genus of moderately halophilic, endospore forming, round bacterium assigned to the phylum Firmicutes and the family Planococcaceae.
A semi-solid composed of suspensions of active and/or inert ingredient(s) in any type of highly viscous material, including gelatin or gel. The…
The middle part of the small intestine. It is between the duodenum (first part of the small intestine) and the ileum (last…
Surgery to create an opening into the jejunum (part of the small intestine) from the outside of the body. A jejunostomy allows…
The formation of tissue in the lumen of the jejunum that results in partial obstruction.
A circumscribed inflammatory and necrotic erosive lesion in the mucosa surface of the jejunum.
