Case Reports
Familial syndrome with dystonia, neural deafness, and possible intellectual impairment: clinical course and pathological findings
- PMID: 181965
Item in Clipboard
Case Reports
Familial syndrome with dystonia, neural deafness, and possible intellectual impairment: clinical course and pathological findings
Adv Neurol.
1976.
No abstract available
Similar articles
-
Dystonia musculorum deformans. Clinical, genetic and pathoanatomical studies.Psychiatr Neurol Neurochir. 1967 Mar-Apr;70(2):77-121. Psychiatr Neurol Neurochir. 1967. PMID: 6050693 No abstract available.
-
Hereditary Parkinsonism-dystonia with sustained control by L-DOPA and anticholinergic medication.Adv Neurol. 1976;14:201-13. Adv Neurol. 1976. PMID: 942621 No abstract available.
-
X-linked Dystonia-Deafness syndrome.Mov Disord. 1998 Mar;13(2):303-8. doi: 10.1002/mds.870130217. Mov Disord. 1998. PMID: 9539345
-
Age, gender, and hemispheric differences in human striatum: a quantitative review and new data from in vivo MRI morphometry.Neurobiol Learn Mem. 1995 Mar;63(2):133-42. doi: 10.1006/nlme.1995.1013. Neurobiol Learn Mem. 1995. PMID: 7663886 Review.
-
Clinical and molecular findings in a patient with a novel mutation in the deafness-dystonia peptide (DDP1) gene.Brain. 2003 Aug;126(Pt 8):1814-20. doi: 10.1093/brain/awg174. Epub 2003 Jun 4. Brain. 2003. PMID: 12805099 Review.
Cited by
-
A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22.J Med Genet. 1995 Apr;32(4):257-63. doi: 10.1136/jmg.32.4.257. J Med Genet. 1995. PMID: 7643352 Free PMC article.
-
Phenotype prediction of Mohr-Tranebjaerg syndrome (MTS) by genetic analysis and initial auditory neuropathy.BMC Med Genet. 2019 Jan 11;20(1):11. doi: 10.1186/s12881-018-0741-3. BMC Med Genet. 2019. PMID: 30634948 Free PMC article.
-
The genetics of primary torsion dystonia.Hum Genet. 1990 Jan;84(2):107-15. doi: 10.1007/BF00208922. Hum Genet. 1990. PMID: 2404852 Review.