Sindrome di Gerstmann
Revisione paritaria di Dr Laurence KnottUltimo aggiornamento di Dr Colin Tidy, MRCGPUltimo aggiornamento 20 Dic 2021
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Synonyms: developmental Gerstmann's syndrome (when it occurs in children), Gerstmann tetrad
The condition should not be confused with Gerstmann-Sträussler syndrome or Gerstmann-Sträussler-Scheinker syndrome - a transmissible spongiform encephalopathy.
What is Gerstmann's syndrome?1 2
Gerstmann's syndrome is a condition arising as a result of disease of the dominant parietal lobe at the angular gyrus3 . Possibly both superior and inferior lobes need to be affected4 . The specific effect of lesions of various lobes is discussed in the separate Lesioni occupanti spazio del cervello article. However, in Gerstmann's syndrome in particular, the result is characterised by four components:
Agraphia or dysgraphia
Acalculia or dyscalculia
Finger agnosia
Left-right disorientation
Pure Gerstmann's syndrome is said to be without aphasia. It generally presents as either a congenital or learning disorder or as a feature of a stroke of the middle cerebral artery. Both forms are rare, especially the childhood form. It can also be a feature of neurodegenerative diseases such as Alzheimer's disease or as a result of head injury.
The childhood type may occur in those with brain damage or in isolation with otherwise good mental function. The pathophysiology in children is not understood. It does not seem to have a genetic component and is not listed in Online Mendelian Inheritance in Man (OMIM). It has been argued that developmental Gerstmann's syndrome is not a unique entity but a feature of other neurodevelopmental disorders5 . This has also been disputed6 . In adults, the risk factors appear to be the same as those for a cerebrovascular event.
Gerstmann's syndrome symptoms
There is loss or absence of four sensory abilities7 :
Loss of the ability to express thoughts in writing (agraphia, dysgraphia).
Inability to perform simple arithmetical calculations (acalculia).
Inability to recognise or indicate one's own or another's fingers (finger agnosia).
Inability to distinguish between right and left.
In addition, many adults also experience aphasia (difficulty in expression with speech, in understanding speech or in reading and writing).
The speech area is in the dominant hemisphere that is on the left in over 95% of right-handed people. It is also on the left in 75% of left-handed people; however, in the other 25% it appears to be bilateral.
Most paediatric cases are identified when children start school and they are challenged with writing and numbers. In addition to the four primary symptoms, many children also have constructional apraxia, an inability to copy simple drawings. Frequently, there is also impairment in reading (dyslexia). Children with good intellectual function as well as those with brain damage may be affected.
Eliciting features of Gerstmann's syndrome
Agraphia:
Illegible or very poor writing.
Inconsistencies in forming letters.
Mixture of upper- and lower-case letters or print and cursory writing.
Irregular letter sizes and shapes.
Unfinished letters.
They struggle to use writing for communication.Acalculia: this is tested by asking the patient to do serial subtraction of 7 from 100. This means 100, 93, 86, 79, 72, etc. It must be interpreted in the light of the educational level of the patient, including the age of a child. An easier test may be applicable, especially for children.
Finger agnosia: finger agnosia is difficulty in distinguishing fingers on the hand. It is tested by requests like, "Touch my index finger with your index finger" and "Touch your nose with your little finger".
Left-right disorientation: this is confusion of the right and left limbs and indicates a lesion in the dominant parietal lobe. It is tested by requests like, "Show me your left hand", "Touch your right foot" and "Touch your left ear with your right hand". A positive test is the inability to obey these commands in the presence of otherwise normal sensory and motor function.
Diagnosi differenziale
In adults, differential diagnosis is that of cerebrovascular events e demenza8 . In children, it is global brain damage and disabilità intellettiva generale.
Indagini
MRI scan will usually show a lesion of the angular gyrus in the left parietal lobe.
Malattie associate
As well as occurring in strokes, head injuries and developmental disorders, the syndrome has been associated with:
Cerebral atrophy
Gerstmann's syndrome treatment and management
There is no cure for Gerstmann's syndrome. Treatment is supportive:
Dysgraphia and apraxia can be helped by occupational and speech therapy. Calculators and word processors can also help school children cope with their disabilities.
There has been a recognition of the association between finger recognition and numerical ability and there has been promising work done where improving finger gnosis through training exercises has led to improvements in the mathematical skills of young children10 .
Prognosi
Gerstmann's syndrome symptoms may lessen in adults over time. This is also thought to occur in children but it is more likely that they adapt to life with them. It has been suggested that early diagnosis and intensive treatment give a better outcome5 .
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Ulteriori letture e riferimenti
- Altabakhi IW, Liang JW; Gerstmann Syndrome. StatPearls, Sept 2021.
- Ardila A; A proposed reinterpretation of Gerstmann's syndrome. Arch Clin Neuropsychol. 2014 Dec;29(8):828-33. doi: 10.1093/arclin/acu056. Epub 2014 Nov 5.
- Rusconi E, Pinel P, Dehaene S, et al; The enigma of Gerstmann's syndrome revisited: a telling tale of the vicissitudes of neuropsychology. Brain. 2010 Feb;133(Pt 2):320-32. doi: 10.1093/brain/awp281. Epub 2009 Nov 10.
- Roux FE, Boetto S, Sacko O, et al; Writing, calculating, and finger recognition in the region of the angular gyrus: a cortical stimulation study of Gerstmann syndrome. J Neurosurg. 2003 Oct;99(4):716-27.
- Russell SM, Elliott R, Forshaw D, et al; Resection of parietal lobe gliomas: incidence and evolution of neurological deficits in 28 consecutive patients correlated to the location and morphological characteristics of the tumor. J Neurosurg. 2005 Dec;103(6):1010-7.
- Miller CJ, Hynd GW; What ever happened to developmental Gerstmann's syndrome? Links to other pediatric, genetic, and neurodevelopmental syndromes. J Child Neurol. 2004 Apr;19(4):282-9.
- Suresh PA, Sebastian S; Developmental Gerstmann's syndrome: a distinct clinical entity of learning disabilities. Pediatr Neurol. 2000 Apr;22(4):267-78.
- Gerstmann's Syndrome; Istituto Nazionale di Disordini Neurologici e Stroke
- Nagaratnam N, Phan TA, Barnett C, et al; Angular gyrus syndrome mimicking depressive pseudodementia. J Psychiatry Neurosci. 2002 Sep;27(5):364-8.
- Jung RE, Yeo RA, Sibbitt WL Jr, et al; Gerstmann syndrome in systemic lupus erythematosus: neuropsychological, neuroimaging and spectroscopic findings. Neurocase. 2001;7(6):515-21.
- Gracia-Bafalluy M, Noel MP; Does finger training increase young children's numerical performance? Cortex. 2008 Apr;44(4):368-75. Epub 2008 Jan 8.
Informazioni sull'autoreVisualizza il profilo completo

Dr Colin Tidy, MRCGP
Medico di base, Autore medico
MBBS, MRCGP, MRCP (Paediatrics), DCH
Il Dr Colin Tidy è un medico del NHS, con sede nell'Oxfordshire.
Informazioni sul recensoreVisualizza il profilo completo

Dr Laurence Knott
Medico di base, Autore medico
Laurea in Biochimica (con lode), MBBS
Il Dr. Laurence Knott si è qualificato nel 1973 e ha avuto una vasta esperienza come Medico Generico.
Storia dell'articolo
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Prossima revisione prevista: 19 Dic 2026
20 Dic 2021 | Ultima versione

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