Benign hereditary chorea (Q41110): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed label, description and/or aliases in pt-br, en |
||
| description / pt-br | description / pt-br | ||
Coreia hereditária benigna deve ser coonsiderada em pessoas com uma coreia relativamente estável e não progressiva, em quem o início na infância e uma história familiar autossômica dominante estão presentes. Coreia hereditária benigna pode estar associada a baixa estatura e atraso do desenvolvimento. Deleções maiores no gene causador, TITF-1, podem causar transtorno multissistêmico com hipotireoidismo congênito, hipotonia e problemas pulmonares. | |||
| description / en | description / en | ||
Benign hereditary chorea should be considered in people with a relatively stable, nonprogressive chorea, in whom childhood onset and an autosomal dominant family history are present. Benign hereditary chorea can be associated with short stature and developmental delay. Larger deletions of causative gene, TITF-1, can cause a multisystem disorder with congenital hypothyroidism, hypotonia, and pulmonary problems. | |||
Revision as of 07:10, 13 August 2026
Benign hereditary chorea should be considered in people with a relatively stable, nonprogressive chorea, in whom childhood onset and an autosomal dominant family history are present. Benign hereditary chorea can be associated with short stature and developmental delay. Larger deletions of causative gene, TITF-1, can cause a multisystem disorder with congenital hypothyroidism, hypotonia, and pulmonary problems.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 8A01.0 |
||
| English | Benign hereditary chorea |
Benign hereditary chorea should be considered in people with a relatively stable, nonprogressive chorea, in whom childhood onset and an autosomal dominant family history are present. Benign hereditary chorea can be associated with short stature and developmental delay. Larger deletions of causative gene, TITF-1, can cause a multisystem disorder with congenital hypothyroidism, hypotonia, and pulmonary problems. |
