Disease #02340 (PSNP1 (ophthalmoplegia, supranuclear, progressive (PSNP-1)), OMIM:601104)

Official abbreviation PSNP1
Name ophthalmoplegia, supranuclear, progressive (PSNP-1)
OMIM ID 601104
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 3
Phenotype entries for this disease 2
Associated with 1 gene MAPT
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00444110 1 PubMed: Ogaki 2012, Journal: Ogaki 2012 46-year-old man with no family history of dementia or movement disorders. M ? Japan Asian 49y - - L-dopa/benserazide (up to 900 mg/day) was ineffective PSNP1 Poor speech, dyspnea, gait disturbance, limb bradykinesia, palilalia, vertical supranuclear gaze palsy, slow saccadic eye movements C9orf72, MAPT MAPT 1 1 PROW_Groep_25
00445373 FamBPat2 PubMed: Ogaki 2012, Journal: Ogaki 2012 family, 2 affected brothers M ? Japan Asian 54y - - L-dopa/benserazide at 200 mg/day mildly alleviated parkinsonism PSNP1 Oscillopsia, micrographia, shuffling gait, horizontal pendular nystagmus, bradykinesia, upper limb postural tremor, postural instability, eyelid apraxia. C9orf72, MAPT MAPT 1 2 PROW_Groep_25
00445392 FamBPat3 PubMed: Ogaki 2012, Journal: Ogaki 2012 brother M ? Japan Asian 56y - - L-dopa/carbidopa at 600 mg/day was not effective PSNP1 Oscillopsia, horizontal pendular nystagmus, mild bradykinesia, postural tremor in both hands and tongue, postural instability, slow saccades, eyelid apraxia. C9orf72, MAPT MAPT 1 1 PROW_Groep_25
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