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6 patient data entries in database for mutation S511N.

Entry
#
Mutations
allele 1allele 2
Clinical representationSymptomsAge groupAge of onsetAge of patientAge of deathReference
509S511N2
PEO, Ptosis, limb ataxia and progressive hearing loss. On examination, she had prominent ptosis, mild bilateral facial weakness, symmetric hip flexion weakness, and absent lower limb tendon reflexes with a mild gait ataxia. axonal sensory neuropathy with additional myopathic features. Muscle biopsy revealed an increased range of muscle fiber diameters, 20% being cytochrome c oxidase–deficient.
-movement disorder (ataxia)
-ptosis
-PEO
-hearing loss
adult
4061n/aHudson et al, 2007;

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510L463F2
S511N2
Presented with fatigue and was noted to have bilateral ptosis since the age of 46 years. He subsequently developed an unsteady gait, progressive deafness, and dysphagia. Extrapyramidal features were first noted 2 years later, at age 48 years, and they progressed until his symptoms improved after receiving ropinirole. He had a history of depression. On examination, he walked with a stooped posture and a shuffling gait with limited arm-swing, slow turning, and postural instability. He had symmetric bradykinesia but no tremor. He had an expressionless face and hypophonia with bilateral ptosis and ophthalmoplegia with relative sparing of downgaze. There were mild symmetric proximal muscle weakness, absent lower limb reflexes, and mild gait ataxia. Parkinsons.
-movement disorder (ataxia)
-muscle weakness
-ptosis
-ophthalmoplegia
-parkinson's disease
-dysphagia
-tremor
adult
4652n/aHudson et al, 2007;

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511S511N2
bilateral ptosis.
-ptosis
adult
n/a60n/aHudson et al, 2007;

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512S511N2
bilateral ptosis.
-ptosis
adult
n/a65n/aHudson et al, 2007;

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513S511N2
bilateral ptosis.
-ptosis
adult
n/a58n/aHudson et al, 2007;

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514S511N2
progressive bilateral ptosis in her early 20s followed by external ophthalmoplegia. She came to medical attention through an infertility clinic investigating her primary ovarian failure.
-ptosis
-ophthalmoplegia
-external ophthalmoplegia
adult
2030n/aHudson et al, 2007;

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1-5 pathogenic cluster assignment of mutations. Mutations displayed without a superscript number are outside of the assigned pathogenic clusters. See cluster definitions for details.

Number of displayed patient cases: 6
Avg age of onset in displayed cases: 48.2
Std dev in onset in displayed cases: 15.2

Search criteria for patient entries:
Mutations Entry IDs Clusters Reference Residue range
Mutations:
Allele 1:Allele 2:
Separate multiple mutations with commas.
Use "PNF" for non-missense mutations.
Match: Inclusive Exact
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