RESUMEN
BACKGROUND: Inherited peripheral neuropathies (IPNs) represent a broad group of genetically and clinically heterogeneous disorders, including axonal Charcot-Marie-Tooth type 2 (CMT2) and hereditary motor neuropathy (HMN). Approximately 60%-70% of cases with HMN/CMT2 still remain without a genetic diagnosis. Interestingly, mutations in HMN/CMT2 genes may also be responsible for motor neuron disorders or other neuromuscular diseases, suggesting a broad phenotypic spectrum of clinically and genetically related conditions. Thus, it is of paramount importance to identify novel causative variants in HMN/CMT2 patients to better predict clinical outcome and progression. METHODS: We designed a collaborative study for the identification of variants responsible for HMN/CMT2. We collected 15 HMN/CMT2 families with evidence for autosomal recessive inheritance, who had tested negative for mutations in 94 known IPN genes, who underwent whole-exome sequencing (WES) analyses. Candidate genes identified by WES were sequenced in an additional cohort of 167 familial or sporadic HMN/CMT2 patients using next-generation sequencing (NGS) panel analysis. RESULTS: Bioinformatic analyses led to the identification of novel or very rare variants in genes, which have not been previously associated with HMN/CMT2 (ARHGEF28, KBTBD13, AGRN and GNE); in genes previously associated with HMN/CMT2 but in combination with different clinical phenotypes (VRK1 and PNKP), and in the SIGMAR1 gene, which has been linked to HMN/CMT2 in only a few cases. These findings were further validated by Sanger sequencing, segregation analyses and functional studies. CONCLUSIONS: These results demonstrate the broad spectrum of clinical phenotypes that can be associated with a specific disease gene, as well as the complexity of the pathogenesis of neuromuscular disorders.
Asunto(s)
Enfermedad de Charcot-Marie-Tooth/genética , Atrofia Muscular Espinal/genética , Adulto , Anciano , Agrina/genética , Enfermedad de Charcot-Marie-Tooth/fisiopatología , Biología Computacional , Enzimas Reparadoras del ADN/genética , Femenino , Secuenciación de Nucleótidos de Alto Rendimiento , Humanos , Péptidos y Proteínas de Señalización Intracelular/genética , Masculino , Persona de Mediana Edad , Complejos Multienzimáticos/genética , Proteínas Musculares/genética , Atrofia Muscular Espinal/fisiopatología , Linaje , Fosfotransferasas (Aceptor de Grupo Alcohol)/genética , Proteínas Serina-Treonina Quinasas/genética , Receptores sigma/genética , Factores de Intercambio de Guanina Nucleótido Rho/genética , Secuenciación del Exoma , Receptor Sigma-1RESUMEN
We detail the phenotype of a novel form of neuronal ceroid lipofuscinosis due to a homozygous progranulin gene mutation (c.813_816del; CLN11 MIM #614706). The symptoms appeared in two young adult siblings, and included progressive retinopathy, recurrent generalized seizures, moderate ataxia, and subtle cognitive dysfunction. Long-lasting episodes of palinopsia were a recurring symptom and associated with polyphasic visual-evoked potential waveform that suggested hyperexcitability of the occipital cortex. Electroencephalography showed rare spike-wave paroxysms, and magnetic resonance imaging revealed selective cerebellar atrophy. Skin biopsy revealed fingerprint storage and the absence of progranulin protein. Electron microscopy of peripheral blood leukocytes showed fingerprint profiles in 1/100 lymphocytes. These findings define a novel phenotype and provide clues for better understanding of progranulin function. A PowerPoint slide summarizing this article is available for download in the Supporting Information section here.
Asunto(s)
Péptidos y Proteínas de Señalización Intercelular/genética , Lipofuscinosis Ceroideas Neuronales/genética , Enfermedades de la Retina/genética , Convulsiones/genética , Atrofia , Encéfalo/patología , Encéfalo/fisiopatología , Cerebelo/patología , Electroencefalografía , Potenciales Evocados Visuales , Humanos , Imagen por Resonancia Magnética , Masculino , Mutación , Neuroimagen , Lipofuscinosis Ceroideas Neuronales/fisiopatología , Fenotipo , Progranulinas , Recurrencia , Hermanos , Adulto JovenRESUMEN
BACKGROUND: Leukodystrophy with vanishing white matter (LVWM) is an autosomal recessive disease with typical pediatric-onset caused by mutations in one of the five EIF2B genes. Adult-onset (AO) cases are rare. METHODS: In this observational study, we reviewed clinical and laboratory information of the patients with AO-LVWM assessed at two referral centers in Italy and Portugal from Jan-2007 to Dec-2019. RESULTS: We identified 18 patients (13 females) with AO-LVWM caused by EIF2B5 or EIF2B3 mutations. Age of neurological onset ranged from 16 to 60 years, with follow-ups occurring from 2 to 37 years. Crucial symptoms were cognitive and motor decline. In three patients, stroke-like events were the first manifestation; in another, bladder dysfunction remained the main complaint across decades. Brain MRI showed white matter (WM) rarefaction in all cases, except two. Diffusion-weighted imaging documented focal hyperintensity in the acute stage of stroke-like events. 1H-spectroscopy primarily showed N-acetyl-aspartate reduction; 18fluorodeoxyglucose-PET revealed predominant frontoparietal hypometabolism; evoked potential studies demonstrated normal-to-reduced amplitudes; neuro-ophthalmological assessment showed neuroretinal thinning, and b-wave reduction on full-field electroretinogram. Interestingly, we found an additional patient with LVWM-compatible phenotype and monoallelic variants in two distinct eIF2B genes, EIF2B1 and EIF2B2. CONCLUSIONS: AO-LVWM presents varying clinical manifestations at onset, including stroke-like events. WM rarefaction is the most consistent diagnostic clue even in the latest onset cases. Spectroscopy and electrophysiological features are compatible with axon, rather than myelin, damage. Cerebral glucose metabolic abnormalities and retinal alterations can be present. LVWM might also be caused by a digenic inheritance affecting the eIF2B complex.
Asunto(s)
Enfermedades Desmielinizantes , Leucoencefalopatías , Enfermedades por Almacenamiento Lisosomal , Enfermedades Neurodegenerativas , Accidente Cerebrovascular , Sustancia Blanca , Adolescente , Adulto , Femenino , Humanos , Masculino , Persona de Mediana Edad , Adulto Joven , Factor 2B Eucariótico de Iniciación/genética , Leucoencefalopatías/diagnóstico por imagen , Leucoencefalopatías/genética , Imagen por Resonancia Magnética , Mutación/genética , Estudios Observacionales como Asunto , Sustancia Blanca/diagnóstico por imagenRESUMEN
The surgical results of this series of occult spina bifida seem better than the natural history registered in the long pre-operative period in terms of neurological deterioration. The major contribution to this result is attributed to neurophysiological monitoring that lowers the risks of permanent damage and increases the percentage of effective detethering. The present series of TCS, due to conus and filar lipoma, documents that CM1 is a really rare association occurring in less than 6% of the patients, despite the low position of conus. The detethering procedure did not influence the tonsillar position, thus excluding the correlation between the tethering and the tonsillar descent. The genetic alteration documented in a girl reinforces the hypothesis of a rare complex polymaformative picture deserving multiple procedures according to the prevailing clinical symptoms.
Asunto(s)
Malformación de Arnold-Chiari/etiología , Procedimientos Neuroquirúrgicos/efectos adversos , Complicaciones Posoperatorias/fisiopatología , Malformación de Arnold-Chiari/cirugía , Preescolar , Electromiografía , Femenino , Humanos , Italia , Estudios Longitudinales , Imagen por Resonancia Magnética , Masculino , Defectos del Tubo Neural/cirugía , Estudios Retrospectivos , Espina Bífida Oculta/cirugíaRESUMEN
We used electroencephalography (EEG)-polygraphic recordings to classify myoclonus in 109 patients with Creutzfeldt-Jakob disease (CJD) on the basis of its electromyography (EMG) pattern, time course, distribution, and EEG correlates. We recorded myoclonic jerks in 55 patients (50.4%), and we classified them as periodic myoclonus in 28, rhythmic in 13, and irregular in 20 (6 patients showed two types of myoclonus). Myoclonus occurred as a prominently negative event (interrupting the EMG discharge) in 10. Periodic sharp-wave complexes (PSWCs) were present in all but one patient with myoclonic jerks but were time-locked with EMG-bursts only in case of periodic myoclonus. Jerk-locked back averaging revealed a variable EEG-EMG transfer-time commonly exceeding that characterizing cortical myoclonus. Myoclonus was frequently associated with Met/Met polymorphism at codon 129 of the prion protein gene, but it was also observed in association with Met/Val or Val/Val polymorphisms provided that the EEG showed the presence of the PSWC pattern. The presence of enlarged somatosensory evoked potentials significantly correlated with the myoclonic presentation, as did MR signal hyperintensity involving the cortical mantle. Our observations on the basis of standard polygraphic criteria suggest that CJD associates with a remarkable variety of myoclonic jerks, and therefore different brain structures are probably involved as generators. The significant association between the presence of all myoclonus types with PSWCs suggests that hyperexcitable corticosubcortical loops are always required to generate (or allow) both myoclonus and the EEG complexes, either they are time locked or not.
Asunto(s)
Encéfalo/fisiopatología , Síndrome de Creutzfeldt-Jakob/complicaciones , Mioclonía/diagnóstico , Anciano , Análisis de Varianza , Síndrome de Creutzfeldt-Jakob/fisiopatología , Electroencefalografía , Electromiografía , Humanos , Masculino , Persona de Mediana Edad , Mioclonía/clasificación , Mioclonía/complicaciones , Mioclonía/fisiopatología , Grabación de Cinta de VideoRESUMEN
We report the atypical presentation of Lafora disease in a Senegalese girl carrying the homozygous variant, c.560A>C, in the NHLRC1 gene. At 13 years, the patient developed myoclonic and visual seizures, progressive psychomotor slowing, and cognitive decline. At 14 years, a neurological examination showed severe hypomimia, bradykinesia, rigidity and low-amplitude myoclonic jerks. Flash-visual and somatosensory evoked potentials showed an increased amplitude of the cortical components, while an electroretinogram showed attenuated responses. An EEG showed diffuse polyspikes associated with positive-negative jerks as well as posterior slow waves and irregular spikes. The electroclinical picture suggested the diagnosis of Lafora disease regarding the association of visual seizures, cognitive deterioration, and action myoclonus, together with the EEG and evoked potential findings. Two uncommon findings were the prominence of extrapyramidal signs in the early stage of disease (which are rarely reported) and attenuation of electroretinal responses. We consider that Lafora disease should be included in the diagnostic work-up for juvenile Parkinsonism, when associated with epilepsy.
Asunto(s)
Disfunción Cognitiva , Enfermedad de Lafora , Trastornos Parkinsonianos , Adolescente , Disfunción Cognitiva/etiología , Disfunción Cognitiva/fisiopatología , Electroencefalografía , Potenciales Evocados/fisiología , Femenino , Humanos , Enfermedad de Lafora/complicaciones , Enfermedad de Lafora/genética , Enfermedad de Lafora/fisiopatología , Trastornos Parkinsonianos/etiología , Trastornos Parkinsonianos/fisiopatología , Retina/fisiopatología , Senegal , Ubiquitina-Proteína Ligasas/genéticaRESUMEN
It has been demonstrated that sagopilone (ZK-EPO) has antitumor activity in human orthotopic glioma models in vitro and in vivo. The objective of this study was to evaluate the safety and efficacy of ZK-EPO in patients with pretreated, recurrent malignant gliomas. Fifteen patients with recurrent malignant gliomas who had received prior surgery, radiotherapy, and >or=2 lines of alkylating chemotherapy were recruited. ZK-EPO (16 mg/m(2)) was administered iv for 3 h every 21 days. The primary end point was six months progression-free survival (PFS-6); secondary end points were safety, toxicity, response rate, and median time to progression (TTP). Magnetic resonance imaging (MRI) evaluations were performed every two cycles and toxicity was evaluated at each cycle using common terminology criteria for adverse events (CTCAE 3.0). A median of four cycles was administered. The median TTP was 13 weeks. PFS-6 was achieved in five patients (33%), three with glioblastoma multiforme and two with anaplastic astrocytoma. The most common treatment-related adverse event was neuropathy, which occurred in 6/15 patients. ZK-EPO had an acceptable safety profile and clinically relevant activity in patients with pretreated, recurrent malignant gliomas.
Asunto(s)
Antineoplásicos/uso terapéutico , Benzotiazoles/uso terapéutico , Neoplasias Encefálicas/tratamiento farmacológico , Epotilonas/uso terapéutico , Glioma/tratamiento farmacológico , Adolescente , Adulto , Anciano , Neoplasias Encefálicas/mortalidad , Esquema de Medicación , Femenino , Glioma/mortalidad , Humanos , Imagen por Resonancia Magnética , Masculino , Persona de Mediana Edad , Índice de Severidad de la Enfermedad , Análisis de Supervivencia , Adulto JovenRESUMEN
Thymoma-associated myasthenia gravis is considered a more severe disease compared with non-thymomatous myasthenia gravis and is generally associated with antibodies to the acetylcholine receptor (AChR-Ab). Even though a single case of thymoma-associated myasthenia gravis with anti-muscle specific kinase (MuSK) antibodies has been reported, to our knowledge, seronegative thymoma-associated myasthenia gravis has not been described. We report on two cases of this disease without antibodies to AChR or MuSK as a further evidence of the variability of myasthenia gravis in terms of antibody profile and thymic pathological findings.
Asunto(s)
Autoanticuerpos/análisis , Miastenia Gravis/metabolismo , Receptores Colinérgicos/inmunología , Receptores Colinérgicos/metabolismo , Timoma/complicaciones , Neoplasias del Timo/complicaciones , Adulto , Femenino , Humanos , Inmunohistoquímica , Masculino , Persona de Mediana Edad , Miastenia Gravis/inmunología , Proteínas Tirosina Quinasas/genética , Proteínas Tirosina Quinasas Receptoras/metabolismo , Timoma/inmunología , Timoma/patología , Neoplasias del Timo/inmunología , Neoplasias del Timo/patología , Tomografía Computarizada por Rayos XRESUMEN
Mutations in the epsilon-sarcoglycan (SGCE) gene have been associated with DYT11 myoclonus-dystonia syndrome (MDS). The aim of this study was to characterize myoclonus in 9 patients with DYT11-MDS presenting with predominant myoclonus and mild dystonia by means of neurophysiological techniques. Variously severe multifocal myoclonus occurred in all of the patients, and included short (mean 89.1 +/- 13.3 milliseconds) electromyographic bursts without any electroencephalographic correlate, sometimes presenting a pseudo-rhythmic course. Massive jerks could be evoked by sudden stimuli in 5 patients, showing a "startle-like" muscle spreading and latencies consistent with a brainstem origin. Somatosensory evoked potentials and long-loop reflexes were normal, as was silent period and long-term intracortical inhibition evaluated by means of transcranial magnetic stimulation; however, short-term intracortical inhibition revealed subtle impairment, and event-related synchronization (ERS) in the beta band was delayed. Blink reflex recovery was strongly enhanced. Myoclonus in DYT11-MDS seems to be generated at subcortical level, and possibly involves basal ganglia and brainstem circuitries. Cortical impairment may depend from subcortical dysfunction, but it can also have a role in influencing the myoclonic presentation. The wide distribution of the defective SCGE in DYT11-MDS may justify the involvement of different brain areas.
Asunto(s)
Trastornos Distónicos/complicaciones , Trastornos Distónicos/genética , Mioclonía/complicaciones , Mioclonía/genética , Neurofisiología/métodos , Estimulación Acústica/métodos , Adolescente , Adulto , Niño , Estimulación Eléctrica/métodos , Electroencefalografía/métodos , Electromiografía/métodos , Potenciales Evocados Somatosensoriales/fisiología , Femenino , Humanos , Masculino , Mutación , Conducción Nerviosa/fisiología , Tiempo de Reacción/fisiología , Reflejo/fisiología , Sarcoglicanos/genética , Estimulación Magnética Transcraneal/métodos , Adulto JovenRESUMEN
We investigated the spatial correspondence between functional MRI (fMRI) activations and cortical current density maps of event-related potentials (ERPs) reconstructed without fMRI priors. The presence of a significant spatial correspondence is a prerequisite for direct integration of the two modalities, enabling to combine the high spatial resolution of fMRI with the high temporal resolution of ERPs. Four separate tasks were employed: visual stimulation with a pattern-reversal chequerboard, recognition of images of nameable objects, recognition of written words, and auditory stimulation with a piano note. ERPs were acquired with 19 recording channels, and source localisation was performed using a realistic head model, a standard cortical mesh and the multiple sparse priors method. Spatial correspondence was evaluated at group level over 10 subjects, by means of a voxel-by-voxel test and a test on the distribution of local maxima. Although not complete, it was significant for the visual stimulation task, image and word recognition tasks (P < 0.001 for both types of test), but not for the auditory stimulation task. These findings indicate that partial but significant spatial correspondence between the two modalities can be found even with a small number of channels, for three of the four tasks employed. Absence of correspondence for the auditory stimulation task was caused by the unfavourable situation of the activated cortex being perpendicular to the overlying scalp, whose consequences were exacerbated by the small number of channels. The present study corroborates existing literature in this field, and may be of particular relevance to those interested in combining fMRI with ERPs acquired with the standard 10-20 system.
Asunto(s)
Corteza Cerebral/fisiología , Potenciales Evocados/fisiología , Imagen por Resonancia Magnética/métodos , Desempeño Psicomotor/fisiología , Estimulación Acústica/métodos , Adulto , Percepción Auditiva/fisiología , Mapeo Encefálico/métodos , Corteza Cerebral/anatomía & histología , Dominancia Cerebral/fisiología , Electroencefalografía/métodos , Femenino , Humanos , Procesamiento de Imagen Asistido por Computador/métodos , Masculino , Persona de Mediana Edad , Pruebas Neuropsicológicas/estadística & datos numéricos , Reconocimiento Visual de Modelos/fisiología , Estimulación Luminosa/métodos , Lectura , Conducta Verbal/fisiología , Percepción Visual/fisiologíaRESUMEN
An 11-year-old girl with nonketotic hyperglycinemia who typically presented with a picture of early myoclonic encephalopathy in the neonatal period is presented in this article. Treated early with sodium benzoate and dextromethorphan, she became seizure-free, while myoclonus persisted. During examination, multifocal rhythmic myoclonic jerks in gamma frequency enhanced by motor activity were noted. Coherence analysis of the electroencephalography-electromyography relationship indicated a cortical origin of the myoclonic jerks. Observation of this case suggests that rhythmic cortical myoclonus may represent a late evolution of this rare disorder.
Asunto(s)
Corteza Cerebral/fisiopatología , Epilepsias Mioclónicas/complicaciones , Hiperglicinemia no Cetósica/complicaciones , Trastornos del Movimiento/complicaciones , Mioclonía/complicaciones , Anticonvulsivantes/uso terapéutico , Niño , Preescolar , Dextrometorfano/uso terapéutico , Progresión de la Enfermedad , Electroencefalografía , Epilepsias Mioclónicas/tratamiento farmacológico , Femenino , Humanos , Hiperglicinemia no Cetósica/tratamiento farmacológico , Lactante , Recién Nacido , Imagen por Resonancia Magnética , Trastornos del Movimiento/tratamiento farmacológico , Mioclonía/tratamiento farmacológico , Benzoato de Sodio/uso terapéutico , SobrevivientesRESUMEN
Myelin protein zero (MPZ) is a major component of compact myelin in peripheral nerves where it plays an essential role in myelin formation and adhesion. MPZ gene mutations are usually responsible for demyelinating neuropathies, namely Charcot-Marie-Tooth (CMT) type 1B, Déjèrine-Sottas neuropathy and congenital hypomyelinating neuropathy. Less frequently, axonal CMT (CMT2) associated with MPZ mutations has been described. We report six patients (one sporadic case and five subjects from two apparently unrelated families) with a late onset, but rapidly progressive, axonal peripheral neuropathy. In all patients, molecular analysis demonstrated a novel heterozygous missense mutation (208C>T) in MPZ exon 2, causing the Pro70Ser substitution in the extracellular domain. The diagnosis of CMT2 associated with MPZ mutations should be considered in both sporadic and familial cases of late onset, progressive polyneuropathy. The mechanism whereby compact myelin protein mutations cause axonal neuropathy remains to be elucidated.
Asunto(s)
Axones/patología , Enfermedad de Charcot-Marie-Tooth/genética , Aberraciones Cromosómicas , Análisis Mutacional de ADN , Genes Dominantes , Proteína P0 de la Mielina/genética , Anciano , Biopsia , Enfermedad de Charcot-Marie-Tooth/diagnóstico , Cromosomas Humanos Par 1 , Enfermedades en Gemelos/diagnóstico , Enfermedades en Gemelos/genética , Exones/genética , Femenino , Tamización de Portadores Genéticos , Pruebas Genéticas , Genotipo , Humanos , Masculino , Microscopía Electrónica , Persona de Mediana Edad , Mutación Missense/genética , Fibras Nerviosas Mielínicas/patología , Examen Neurológico , Fenotipo , Nervio Sural/patologíaRESUMEN
PURPOSE: we characterized multifocal myoclonus in Dravet syndrome (DS) that was never systematically typified before. METHODS: we studied EEG-EMG recordings of 19 consecutive patients, aged 2-29 years, with DS associated with SCN1A gene mutations to detect and evaluate myoclonus based on the spectrum of EMG activity on antagonist muscle pairs and cortico-muscular coherence (CMC). RESULTS: multifocal action myoclonus was detected in all patients corresponding to brief EMG bursts, which occurred synchronously on antagonist muscles at a frequency peaking in beta band. There was significant CMC in beta band, and a cortico-muscular transfer time consistent with a cortical origin of the jerks. The somatosensory evoked potentials (SSEPs) were giant in only one patient who also showed exaggerated long-loop reflexes (LLRs). The nine patients who had experienced myoclonic seizures showed greater CMC. CONCLUSIONS: The cortical myoclonus consistently observed in patients with DS shows features that are similar to those characterizing progressive myoclonus epilepsy, but differs because it does not have a severely worsening course and is not commonly associated with increased SSEPs or enhanced LLRs. This kind of myoclonus is an intrinsic feature of DS associated with SCN1A mutations, and may be a cause of disability. SIGNIFICANCE: We hypothesize that myoclonus is generated in cortical motor areas by hyper-synchronous oscillations, which are possibly due to sodium channel dysfunction.
Asunto(s)
Epilepsias Mioclónicas/fisiopatología , Movimiento/fisiología , Mioclonía/fisiopatología , Adolescente , Adulto , Encéfalo/fisiopatología , Niño , Preescolar , Electroencefalografía , Electromiografía , Epilepsias Mioclónicas/genética , Potenciales Evocados Somatosensoriales , Humanos , Músculo Esquelético/fisiopatología , Canal de Sodio Activado por Voltaje NAV1.1/genética , Procesamiento de Señales Asistido por Computador , Adulto JovenAsunto(s)
Síndromes Paraneoplásicos del Sistema Nervioso/fisiopatología , Plexo Braquial/fisiopatología , Diagnóstico Diferencial , Progresión de la Enfermedad , Potenciales Evocados Somatosensoriales , Femenino , Lateralidad Funcional , Humanos , Persona de Mediana Edad , Conducción Nerviosa , Síndromes Paraneoplásicos del Sistema Nervioso/diagnóstico , Nervio Sural/fisiopatologíaRESUMEN
This report describes a male infant who developed right upper limb palsy 5 days after birth and contralateral paralysis at 14 days. Abnormal in utero posture of the right arm had resulted in a difficult cephalic delivery. Right shoulder osteomyelitis was diagnosed at age 16 days from clinical, hematologic, and radiologic findings. Antibiotics were administered, followed by complete resolution of the symptoms in 2 weeks. Electromyographic and nerve conduction studies demonstrated direct involvement of the right brachial plexus, secondary to the osteomyelitis, explaining the unilateral onset and the persistent neurogenic pattern involving the muscles innervated by the right posterior branch to the brachial plexus. However, somatosensory evoked potentials indicated damage to the cervical spinal cord likely related to the birth trauma, which in all likelihood was the cause of the left limb palsy and contributed to the right limb picture.
Asunto(s)
Húmero/diagnóstico por imagen , Osteomielitis/diagnóstico por imagen , Parálisis/diagnóstico por imagen , Brazo , Electromiografía , Humanos , Lactante , Recién Nacido , Nervio Mediano/fisiopatología , Conducción Nerviosa , Osteomielitis/etiología , Osteomielitis/fisiopatología , Parálisis/etiología , Parálisis/fisiopatología , Radiografía , Nervio Cubital/fisiopatologíaRESUMEN
Spinal and bulbar muscular atrophy is an X-linked neuromuscular disease caused by a trinucleotide CAG repeat expansion in the androgen receptor gene; it is clinically characterized by adult-onset, slowly progressive weakness and atrophy mainly affecting proximal limb and bulbar muscles. Charcot-Marie-Tooth disease type 1A is an autosomal dominant polyneuropathy due to peripheral myelin protein 22 gene duplication and characterized by slowly progressive distal limb muscle weakness, atrophy and sensory loss with foot deformities. Here we report the co-occurrence of both neuromuscular genetic diseases in the same male patient. Difficulties in climbing stairs and jaw weakness were presenting symptoms consistent with SBMA. However, predominant distal weakness and bilateral pes cavus were rather suggestive of a hereditary polyneuropathy. The combination of two diseases, even if extremely rare, should be considered in the presence of atypical symptoms; in the case of genetic diseases this event may have important implications on family members' counseling.
Asunto(s)
Enfermedad de Charcot-Marie-Tooth/complicaciones , Enfermedad de Charcot-Marie-Tooth/diagnóstico , Trastornos Musculares Atróficos/complicaciones , Trastornos Musculares Atróficos/diagnóstico , Enfermedad de Charcot-Marie-Tooth/genética , Comorbilidad , Humanos , Masculino , Persona de Mediana Edad , Trastornos Musculares Atróficos/genéticaRESUMEN
OBJECTIVES: To describe the clinical and neurophysiologic patterns of patients with neuronal ceroid lipofuscinoses associated with CLN6 mutations. METHODS: We reviewed the features of 11 patients with different ages at onset. RESULTS: Clinical disease onset occurred within the first decade of life in 8 patients and in the second and third decades in 3. All children presented with progressive cognitive regression associated with ataxia and pyramidal and extrapyramidal signs. Recurrent seizures, visual loss, and myoclonus were mostly reported after a delay from onset; 7 children were chairbound and had severe dementia less than 4 years from onset. One child, with onset at 8 years, had a milder course. Three patients with a teenage/adult onset presented with a classic progressive myoclonic epilepsy phenotype that was preceded by learning disability in one. The EEG background was slow close to disease onset in 7 children, and later showed severe attenuation; a photoparoxysmal response (PPR) was present in all. The 3 teenage/adult patients had normal EEG background and an intense PPR. Early attenuation of the electroretinogram was seen only in children with onset younger than 5.5 years. Somatosensory evoked potentials were extremely enlarged in all patients. CONCLUSIONS: In all patients, multifocal myoclonic jerks and seizures were a key feature, but myoclonic seizures were an early and prominent sign in the teenage/adult form only. Conversely, the childhood-onset form was characterized by initial and severe cognitive impairment coupled with electroretinogram and EEG attenuation. Cortical hyperexcitability, shown by the PPR and enlarged somatosensory evoked potentials, was a universal feature.