| CAMAK | cataract-microcephaly-arthrogryposis-kyphosis [syndrome] |
|---|---|
| CASS | cataract-alopecia-sclerodactyly syndrome; Coronary Artery Surgery Study |
| CAT | California Achievement Test; capillary agglutination test; catalase; cataract; catecholamine; Childr... |
| cat | catalysis, catalyst; cataract |
| CC | calcaneal-cuboid; calcium cyclamate; cardiac catheterization; cardiac contusion; cardiac cycle; card... |
| juvenile chronic arthritis | juvenile arthritis |
|---|---|
| juvenile chronic arthritis, systemic-onset | See: Juvenile rheumatoid arthritis, systemic-onset (still's disease). (12 Dec 1998) |
| juvenile cirrhosis | <pathology> This is a form of continuing liver inflammation that results in liver cell death. Causes include viral infection (hepatitis D, hepatitis B, hepatitis C), autoimmune disease, drug ingestion or metabolic causes. Chronic active hepatitis will lead to hepatic failure and death in a small percentage of these patients. (27 Sep 1997) |
| juvenile delinquency | The antisocial acts of children or persons under age which are illegal or lawfully interpreted as constituting delinquency. (12 Dec 1998) |
| juvenile delinquent | A minor who cannot be controlled by parental authority and commits antisocial or criminal acts, such as vandalism, violence, or robbery. (05 Mar 2000) |
| juvenile diabetes | <endocrinology> A severe metabolic disorder which has an abrupt onset before the age of twenty. In it, an insulin deficiency prevents the body from using carbohydrates properly and forces it to rely mainly on protein metabolism. Treatment of the disease includes strict dietary regulation and mandatory insulin injections. (09 Oct 1997) |
| juvenile elastoma | <dermatology> A connective tissue nevus characterised by an increase in the number and size of the elastic fibres. See: osteodermatopoikilosis. (05 Mar 2000) |
| juvenile epithelial corneal dystrophy | Epithelial dystrophy characterised by progressive cysts and opacities of the corneal epithelium, with onset in infancy. Inheritance: autosomal dominant with incomplete penetrance. Synonym: Meesman dystrophy. (22 Sep 2002) |
| juvenile haemangiofibroma | <oncology, tumour> A benign tumour of the posterior nasopharynx that is most common in adolescent boys. Symptoms repeated epistaxis, nasal congestion, nasal discharge and hearing loss. A skull X-ray or a CT scan of the head can confirm the presence of an angiofibroma. Treatment may include the surgical removal of the lesion if it is enlarging or blocking the airway. (27 Sep 1997) |
| juvenile hormone | <endocrinology> A hormone found in insects which affects the balance between mature and juvenile attributes of certain tissues at each moult. In particular, the imaginal discs of many larval insects only develop into adult wings, sexual organs or limbs when blood juvenile hormone levels fall below a threshold level. There is a complex interaction between juvenile hormone and ecdysone. Synthetic analogues of JH include farnesol and methoprene, which have been tested for insecticide potential (known, with diflubenzuron, as Insect Growth Regulators, IGRs. See: chitin). (18 Nov 1997) |
| juvenile hormone esterase | <enzyme> Amino acid sequence has been determined Registry number: EC 3.1.1.- Synonym: jh esterase, insect jhe (26 Jun 1999) |
| juvenile hormones | Compounds, either natural or synthetic, which block development of the growing insect. (12 Dec 1998) |
| juvenile hyalin fibromatosis | A rare recessively inherited deforming disorder of head, neck, and generalised cutaneous nodules or tumours in children with normal mentality; the lesions consist of fibroblasts separated by an eosinophilic hyalin stroma composed mostly of glycosaminoglycans. Synonym: systemic hyalinosis. (05 Mar 2000) |
| juvenile kyphosis | Osteochondrosis of the vertebral epiphyses in children. (12 Dec 1998) |
| juvenile muscular atrophy | Slowly progressive proximal muscular weakness and wasting, beginning in childhood, caused by degeneration of motor neurons in the anterior horns of the spinal cord; onset usually between 2 and 17 years of age; usually autosomal recessive inheritance. Synonym: juvenile muscular atrophy, Kugelberg-Welander disease, Wohlfart-Kugelberg-Welander disease. (05 Mar 2000) |