Duchenne’s / Becker’s muscular atrophy
| Description | (1 in 3500 male newborns is affected) CK (> 10 times the normal value) Molecular-genetic evaluation is possible. Evidence of deletion in the dystrophin-gene (region Xp21) (70 % of all patients) |
More Results for the letter D
- Dermatitis herpetiformis (Duhring)
- Dermatitis, atopic
- Dermatomyosis
- Desensibilisation
- Diabetes insipidus
- Diabetes mellitus
- Diarrhea, acute
- Diarrhea, chronic
- Discoid lupus erythematosus
- Disturbance of growth
- Dizziness
- Down syndrome, prenatal diagnostic
- Dressler syndrome
- Dubin-Johnson syndrome
- Duchenne’s / Becker’s muscular atrophy
- Duodenal carcinoma
- Duodenal ulcers
- Dysbacteria
- Dyspepsia coli
- Dyspepsia, functional
- Dystrophia myotonica (Steinert syndrome)