U M Bracale, M Di Filippo, A De Capua, L Vanni, D Narese, F Pecoraro, A M Giribono, R Bracale
Angioplasty with drug-coated balloon (DCB) is an emerging and reliable method for the treatment of femoro-popliteal lesions. We report our experience with the Stellarex™ DCB in the first 50 patients.
Methods: From July 2015 to November 2017, 50 patients (41 M, 9F), medium age (64 ± 7.4 year) were subject to 33 angioplasties (PTAs) for femoro-popliteal lesions with a paclitaxel-coated balloon (Stellarex™). Based upon clinical data sixteen patients had severe claudication (56% - Rutherford class 3); ten patients suffered from ischemic rest pain (34% - Rutherford class 4); and five presented minor tissue loss (10% - Rutherford class 5). 42% of patients showed femoro-popliteal lesion TASC-II B, and 58% presented lesions pertaining to TASC-II C.
Results: Immediate technical success was 100% without perioperative complications. Primary patency rate was 94% at twelve months. In three cases restenosis (6%) was detected within a year from procedure, and a further PTA DCB was performed with primary assisted patency rates of 100% at twelve months. Two patients underwent major lower limb amputation. Three patients died during follow-up and one patient was lost at follow-up.
Conclusion: DCB angioplasty with Stellarex™ is a viable alternative to traditional endovascular procedures proving satisfactory primary patency rates at twelve months. Based on our experience, treatment with DCB is a first choice technique for non-complex de novo lesions of the femoro - popliteal tract.
药物包被球囊血管成形术(DCB)是一种新兴的、可靠的治疗股腘窝病变的方法。我们报告了我们在前50名患者中使用Stellarex™DCB的经验。方法:2015年7月至2017年11月,采用紫杉醇包被球囊(Stellarex™)对50例(41 M, 9F)中年龄(64±7.4岁)患者行33例股骨-腘动脉病变血管成形术(pta)。根据临床资料,16例患者有严重跛行(56% - Rutherford分类3);10例患者出现缺血性休息痛(34% - Rutherford分类4);42%的患者表现为股腘窝TASC-II B型病变,58%的患者表现为TASC-II c型病变。结果:立即技术成功率为100%,无围手术期并发症。12个月时原发性通畅率为94%。其中3例(6%)在手术后一年内发现再狭窄,并在12个月时进行了PTA DCB,主要辅助通畅率为100%。2例患者行下肢大截肢。3例患者在随访中死亡,1例患者在随访中丢失。结论:采用Stellarex™的DCB血管成形术是传统血管内手术的可行替代方案,在12个月时具有令人满意的初级通畅率。根据我们的经验,DCB治疗是非复杂的股腘束新发病变的首选技术。
{"title":"Treatment of <i>de novo</i> femoro-popliteal lesions with a new Drug Coated Balloon: early experience of a single Center in the first 50 patients.","authors":"U M Bracale, M Di Filippo, A De Capua, L Vanni, D Narese, F Pecoraro, A M Giribono, R Bracale","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Angioplasty with drug-coated balloon (DCB) is an emerging and reliable method for the treatment of femoro-popliteal lesions. We report our experience with the Stellarex™ DCB in the first 50 patients.</p><p><strong>Methods: </strong>From July 2015 to November 2017, 50 patients (41 M, 9F), medium age (64 ± 7.4 year) were subject to 33 angioplasties (PTAs) for femoro-popliteal lesions with a paclitaxel-coated balloon (Stellarex™). Based upon clinical data sixteen patients had severe claudication (56% - Rutherford class 3); ten patients suffered from ischemic rest pain (34% - Rutherford class 4); and five presented minor tissue loss (10% - Rutherford class 5). 42% of patients showed femoro-popliteal lesion TASC-II B, and 58% presented lesions pertaining to TASC-II C.</p><p><strong>Results: </strong>Immediate technical success was 100% without perioperative complications. Primary patency rate was 94% at twelve months. In three cases restenosis (6%) was detected within a year from procedure, and a further PTA DCB was performed with primary assisted patency rates of 100% at twelve months. Two patients underwent major lower limb amputation. Three patients died during follow-up and one patient was lost at follow-up.</p><p><strong>Conclusion: </strong>DCB angioplasty with Stellarex™ is a viable alternative to traditional endovascular procedures proving satisfactory primary patency rates at twelve months. Based on our experience, treatment with DCB is a first choice technique for non-complex <i>de novo</i> lesions of the femoro - popliteal tract.</p>","PeriodicalId":54170,"journal":{"name":"Translational Medicine at UniSa","volume":"18 ","pages":"3-8"},"PeriodicalIF":1.5,"publicationDate":"2019-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6350779/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"36973419","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
[This corrects the article on p. 25 in vol. 17, PMID: 30083520.].
[这是对第17卷第25页文章的更正,PMID: 30083520]。
{"title":"Errata corrige.","authors":"","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>[This corrects the article on p. 25 in vol. 17, PMID: 30083520.].</p>","PeriodicalId":54170,"journal":{"name":"Translational Medicine at UniSa","volume":"18 ","pages":"9"},"PeriodicalIF":1.5,"publicationDate":"2019-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6350780/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"36973420","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Pediatric Anesthesia.","authors":"S Tesoro, L Marchesini, E De Robertis","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":54170,"journal":{"name":"Translational Medicine at UniSa","volume":"20 ","pages":"1-3"},"PeriodicalIF":1.1,"publicationDate":"2019-01-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6910147/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37468778","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
M. Malamisura, R. Colantuono, V. Salvati, R. Croce, G. D’Adamo, T. Passaro, E. D’Angelo, M. Boffardi, A. Garzi, B. Malamisura
According to the 2012 ESPGHAN criteria for diagnosis of celiac disease (CD), duodenal biopsy (DB) can be avoided in children with a clear malabsorption syndrome, anti-tissue transglutaminase IgA (tTG2) ≥ 10x the cut-off, anti-endomysium IgA (EMA) and HLA DQ2/DQ8 genes. The aim of this study is to report our experience and evaluate the accuracy of the actual guidelines. Patients and methods This is a retrospective study conducted on all patients diagnosed CD from 2012 to 2018 in our Center. For all patients enrolled were analyzed: data of family history, symptoms, serology, genetics, Marsh grade and follow-up. Results A total of 481 children [mean age 6,4 yrs; F:M= 1.8:1] were included in the study. The mean age of patients who were not subject to DB was lower (4.51 yrs) comparing with patients that received DB (6.48 yrs). Out of the 256 patients with anti-tTG2 ≥ 10 fold, 121 underwent DB because of mild symptoms (84/121) or no symptoms (37/121). In all cases Marsh type 3 was found and HLA haplotypes was compatible with CD diagnosis. Conclusions Our study confirms that the serology has a primary importance to diagnose CD, regardless of the symptoms. These data suggest that biopsy and HLA haplotypes search, in presence of anti-tTG2 IgA ≥ 10x the cut-off, are wasteful and unhelpful for the patients.
{"title":"Current Espghan Guidelines for Celiac Disease in Pediatric Age, Tertiary Care Center Experience: A Proposal for Further Simplification","authors":"M. Malamisura, R. Colantuono, V. Salvati, R. Croce, G. D’Adamo, T. Passaro, E. D’Angelo, M. Boffardi, A. Garzi, B. Malamisura","doi":"10.14273/UNISA-2794","DOIUrl":"https://doi.org/10.14273/UNISA-2794","url":null,"abstract":"According to the 2012 ESPGHAN criteria for diagnosis of celiac disease (CD), duodenal biopsy (DB) can be avoided in children with a clear malabsorption syndrome, anti-tissue transglutaminase IgA (tTG2) ≥ 10x the cut-off, anti-endomysium IgA (EMA) and HLA DQ2/DQ8 genes. The aim of this study is to report our experience and evaluate the accuracy of the actual guidelines. Patients and methods This is a retrospective study conducted on all patients diagnosed CD from 2012 to 2018 in our Center. For all patients enrolled were analyzed: data of family history, symptoms, serology, genetics, Marsh grade and follow-up. Results A total of 481 children [mean age 6,4 yrs; F:M= 1.8:1] were included in the study. The mean age of patients who were not subject to DB was lower (4.51 yrs) comparing with patients that received DB (6.48 yrs). Out of the 256 patients with anti-tTG2 ≥ 10 fold, 121 underwent DB because of mild symptoms (84/121) or no symptoms (37/121). In all cases Marsh type 3 was found and HLA haplotypes was compatible with CD diagnosis. Conclusions Our study confirms that the serology has a primary importance to diagnose CD, regardless of the symptoms. These data suggest that biopsy and HLA haplotypes search, in presence of anti-tTG2 IgA ≥ 10x the cut-off, are wasteful and unhelpful for the patients.","PeriodicalId":54170,"journal":{"name":"Translational Medicine at UniSa","volume":"20 1","pages":"13 - 18"},"PeriodicalIF":1.5,"publicationDate":"2019-01-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42318557","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
C Cassandro, A Manassero, A Scarpa, V Landi, G Aschero, S Lovallo, P Velardo, P De Luca, A Albera, R Albera, E Cassandro
{"title":"Auditory-Verbal Processing Disorder and Dyslexia in Adulthood.","authors":"C Cassandro, A Manassero, A Scarpa, V Landi, G Aschero, S Lovallo, P Velardo, P De Luca, A Albera, R Albera, E Cassandro","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":54170,"journal":{"name":"Translational Medicine at UniSa","volume":"20 ","pages":"28-31"},"PeriodicalIF":1.1,"publicationDate":"2019-01-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6910146/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37468139","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
M Malamisura, R Colantuono, V M Salvati, R Croce, G D'Adamo, T Passaro, E D'Angelo, M Boffardi, A Garzi, B Malamisura
According to the 2012 ESPGHAN criteria for diagnosis of celiac disease (CD), duodenal biopsy (DB) can be avoided in children with a clear malabsorption syndrome, anti-tissue transglutaminase IgA (tTG2) ≥ 10x the cut-off, anti-endomysium IgA (EMA) and HLA DQ2/DQ8 genes. The aim of this study is to report our experience and evaluate the accuracy of the actual guidelines.
Patients and methods: This is a retrospective study conducted on all patients diagnosed CD from 2012 to 2018 in our Center. For all patients enrolled were analyzed: data of family history, symptoms, serology, genetics, Marsh grade and follow-up.
Results: A total of 481 children [mean age 6,4 yrs; F:M= 1.8:1] were included in the study. The mean age of patients who were not subject to DB was lower (4.51 yrs) comparing with patients that received DB (6.48 yrs). Out of the 256 patients with anti-tTG2 ≥ 10 fold, 121 underwent DB because of mild symptoms (84/121) or no symptoms (37/121). In all cases Marsh type 3 was found and HLA haplotypes was compatible with CD diagnosis.
Conclusions: Our study confirms that the serology has a primary importance to diagnose CD, regardless of the symptoms. These data suggest that biopsy and HLA haplotypes search, in presence of anti-tTG2 IgA ≥ 10x the cut-off, are wasteful and unhelpful for the patients.
{"title":"Current Espghan Guidelines for Celiac Disease in Pediatric Age, Tertiary Care Center Experience: A Proposal for Further Simplification.","authors":"M Malamisura, R Colantuono, V M Salvati, R Croce, G D'Adamo, T Passaro, E D'Angelo, M Boffardi, A Garzi, B Malamisura","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>According to the 2012 ESPGHAN criteria for diagnosis of celiac disease (CD), duodenal biopsy (DB) can be avoided in children with a clear malabsorption syndrome, anti-tissue transglutaminase IgA (tTG2) ≥ 10x the cut-off, anti-endomysium IgA (EMA) and HLA DQ2/DQ8 genes. The aim of this study is to report our experience and evaluate the accuracy of the actual guidelines.</p><p><strong>Patients and methods: </strong>This is a retrospective study conducted on all patients diagnosed CD from 2012 to 2018 in our Center. For all patients enrolled were analyzed: data of family history, symptoms, serology, genetics, Marsh grade and follow-up.</p><p><strong>Results: </strong>A total of 481 children [mean age 6,4 yrs; F:M= 1.8:1] were included in the study. The mean age of patients who were not subject to DB was lower (4.51 yrs) comparing with patients that received DB (6.48 yrs). Out of the 256 patients with anti-tTG2 ≥ 10 fold, 121 underwent DB because of mild symptoms (84/121) or no symptoms (37/121). In all cases Marsh type 3 was found and HLA haplotypes was compatible with CD diagnosis.</p><p><strong>Conclusions: </strong>Our study confirms that the serology has a primary importance to diagnose CD, regardless of the symptoms. These data suggest that biopsy and HLA haplotypes search, in presence of anti-tTG2 IgA ≥ 10x the cut-off, are wasteful and unhelpful for the patients.</p>","PeriodicalId":54170,"journal":{"name":"Translational Medicine at UniSa","volume":"20 ","pages":"13-18"},"PeriodicalIF":1.1,"publicationDate":"2019-01-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6910143/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37468141","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
A Garzi, G Ardimento, U Ferrentino, S Brongo, R M Di Crescenzo, E Calabrò, M S Rubino, B Malamisura, E Clemente
Gastro-oesophageal reflux is common in children, especially in the first year of life, and it may be regarded as physiological. Good functioning of the lower oesophageal sphincter depends largely on the anatomical relationships between oesophagus, stomach and diaphragm hiatus. Relative immaturity of these structures in newborn babies and young children is a risk factor in reflux disease, which may result in a wide variety of typical and/or atypical symptoms and, sometimes, serious complications such as oesophagitis and stenosis. Reflux disease may be diagnosed and studied, basing on morphological and functional aspects and, since the advent of pH-metry, it is possible to personalise the therapeutic approach to children with reflux. Surgical treatment of reflux disease in children has recently been improved due to a mini-invasive surgical approach. Absolute indications are recurrent pneumonia, intractable pain due to oesophagitis and retarded growth, often in association with neurological impairment. In the last three years, 18 children with reflux disease underwent videolaparoscopic surgery in our department, 14 by the Nissen and 4 by the Toupet technique. Post-operative pH-metry always showed a reduction in exposure of the distal oesophagus to acid (integral of H+) and an improvement in oesophageal clearance (short refluxes percentage) indicative of good functioning of the gastro-oesophageal junction. PH-metry proved to be an invaluable technique for planning therapeutic strategy. In follow-up evaluations, it enabled us to monitor functioning of the gastro-oesophageal junction and to avoid other more difficult and invasive tests in patients with severe neurological impairment.
{"title":"Pre and Post-Operative Ph-Metry in Videolaparoscopic Surgery for Gastro Oesophageal Reflux Disease.","authors":"A Garzi, G Ardimento, U Ferrentino, S Brongo, R M Di Crescenzo, E Calabrò, M S Rubino, B Malamisura, E Clemente","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Gastro-oesophageal reflux is common in children, especially in the first year of life, and it may be regarded as physiological. Good functioning of the lower oesophageal sphincter depends largely on the anatomical relationships between oesophagus, stomach and diaphragm hiatus. Relative immaturity of these structures in newborn babies and young children is a risk factor in reflux disease, which may result in a wide variety of typical and/or atypical symptoms and, sometimes, serious complications such as oesophagitis and stenosis. Reflux disease may be diagnosed and studied, basing on morphological and functional aspects and, since the advent of pH-metry, it is possible to personalise the therapeutic approach to children with reflux. Surgical treatment of reflux disease in children has recently been improved due to a mini-invasive surgical approach. Absolute indications are recurrent pneumonia, intractable pain due to oesophagitis and retarded growth, often in association with neurological impairment. In the last three years, 18 children with reflux disease underwent videolaparoscopic surgery in our department, 14 by the Nissen and 4 by the Toupet technique. Post-operative pH-metry always showed a reduction in exposure of the distal oesophagus to acid (integral of H+) and an improvement in oesophageal clearance (short refluxes percentage) indicative of good functioning of the gastro-oesophageal junction. PH-metry proved to be an invaluable technique for planning therapeutic strategy. In follow-up evaluations, it enabled us to monitor functioning of the gastro-oesophageal junction and to avoid other more difficult and invasive tests in patients with severe neurological impairment.</p>","PeriodicalId":54170,"journal":{"name":"Translational Medicine at UniSa","volume":"20 ","pages":"19-21"},"PeriodicalIF":1.1,"publicationDate":"2019-01-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6910148/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37468215","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
[This corrects the article on p. 27 in vol. 19, PMID: 31360664.].
[这是对第19卷第27页文章的更正,PMID: 31360664]。
{"title":"Errata corrige.","authors":"","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>[This corrects the article on p. 27 in vol. 19, PMID: 31360664.].</p>","PeriodicalId":54170,"journal":{"name":"Translational Medicine at UniSa","volume":"20 ","pages":"32"},"PeriodicalIF":1.5,"publicationDate":"2019-01-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6910144/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37468143","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
C. Cassandro, A. Manassero, A. Scarpa, V. Landi, G. Aschero, S. Lovallo, P. Velardo, P. De Luca, A. Albera, R. Albera, E. Cassandro
28 Università degli Studi di Salerno Introduction According to the Diagnostic and Statistic Manual of Mental Disorders (DSM-V), the neurodevelopment disorders are characterised by an atypical development of some cognitive domains, with a dysfunctional behavioural correlation supported by phenotypes with a genetic connection. Among these are the specific learning disabilities, which are united by a single condition characterised by difficulty in learning and using academic skills in the presence of an adequate IQ; these include dyslexia, dyscalculia and dysorthography. The clinical features are an inaccurate or slow and laborious reading of the words, difficulty in understanding the meaning of what is read, difficulty in spelling, in written expression, in mastering the concept of number, numerical data ora calculation, and in arithmetic reasoning. Recently, thanks to the better understanding of the neurobiological mechanisms underlying these disorders and thanks to the improvement of neuroimaging and genetic analysis, we better understood the evolution of these pathologies and consequently we have refined the diagnosis and treatment. Studies focused particularly more on dyslexia, both due to its high frequency in general population and to the better understanding of its pathogenesis. Various cognitive models are developed to explain the nature of the processes underlying the recognition of written words; the models explained partially the cause of dyslexia, tracing it back to a phonological deficit of consciousness. Today none of these models seems to prevail, but we believe that, in the context of a general reading disorder, there are several difficulties that can be either phonological or about phonological, motor or visual consciousness, due to the failure of magnocellular/auditory neurons development, because of an altered central processing. Already in the 80s, Tallal et al. recognised the phonological deficit as a symptom of a deficit of sound processing presented in rapid sequence (proper of verbal oral language) and therefore a deficit of elaboration at the auditory temporal cortex. This difficulty in the sounds analysis could lead to a wrong categorization and to a failure to recognise the phoneme as the acoustic characteristics change. From studies carried out on children with dyslexia, deficient performances emerged in conditions of short auditory stimuli presented in rapid sequence, while the performance improved with a longer stimulus interval. These difficulties lead to a need for longer times to discriminate short sounds in rapid sequence. Tallal deduced that children with dyslexia presented not a linguistic deficit but a deficit of temporal elaboration of the variation of the auditory patterns, which then translated into a difficulty in the perception of isolated language. In auditory perception of sounds, both when proposed in rapid sequences and with a longer time intervals, a primary role is played by auditory attention, expeci
{"title":"Auditory-Verbal Processing Disorder and Dyslexia in Adulthood","authors":"C. Cassandro, A. Manassero, A. Scarpa, V. Landi, G. Aschero, S. Lovallo, P. Velardo, P. De Luca, A. Albera, R. Albera, E. Cassandro","doi":"10.14273/UNISA-2791","DOIUrl":"https://doi.org/10.14273/UNISA-2791","url":null,"abstract":"28 Università degli Studi di Salerno Introduction According to the Diagnostic and Statistic Manual of Mental Disorders (DSM-V), the neurodevelopment disorders are characterised by an atypical development of some cognitive domains, with a dysfunctional behavioural correlation supported by phenotypes with a genetic connection. Among these are the specific learning disabilities, which are united by a single condition characterised by difficulty in learning and using academic skills in the presence of an adequate IQ; these include dyslexia, dyscalculia and dysorthography. The clinical features are an inaccurate or slow and laborious reading of the words, difficulty in understanding the meaning of what is read, difficulty in spelling, in written expression, in mastering the concept of number, numerical data ora calculation, and in arithmetic reasoning. Recently, thanks to the better understanding of the neurobiological mechanisms underlying these disorders and thanks to the improvement of neuroimaging and genetic analysis, we better understood the evolution of these pathologies and consequently we have refined the diagnosis and treatment. Studies focused particularly more on dyslexia, both due to its high frequency in general population and to the better understanding of its pathogenesis. Various cognitive models are developed to explain the nature of the processes underlying the recognition of written words; the models explained partially the cause of dyslexia, tracing it back to a phonological deficit of consciousness. Today none of these models seems to prevail, but we believe that, in the context of a general reading disorder, there are several difficulties that can be either phonological or about phonological, motor or visual consciousness, due to the failure of magnocellular/auditory neurons development, because of an altered central processing. Already in the 80s, Tallal et al. recognised the phonological deficit as a symptom of a deficit of sound processing presented in rapid sequence (proper of verbal oral language) and therefore a deficit of elaboration at the auditory temporal cortex. This difficulty in the sounds analysis could lead to a wrong categorization and to a failure to recognise the phoneme as the acoustic characteristics change. From studies carried out on children with dyslexia, deficient performances emerged in conditions of short auditory stimuli presented in rapid sequence, while the performance improved with a longer stimulus interval. These difficulties lead to a need for longer times to discriminate short sounds in rapid sequence. Tallal deduced that children with dyslexia presented not a linguistic deficit but a deficit of temporal elaboration of the variation of the auditory patterns, which then translated into a difficulty in the perception of isolated language. In auditory perception of sounds, both when proposed in rapid sequences and with a longer time intervals, a primary role is played by auditory attention, expeci","PeriodicalId":54170,"journal":{"name":"Translational Medicine at UniSa","volume":"20 1","pages":"28 - 31"},"PeriodicalIF":1.5,"publicationDate":"2019-01-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44053677","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
C Cassandro, P De Luca, M Ralli, F Gioacchini, F Di Berardino, A Albera, R Albera, E Cassandro, A Scarpa
{"title":"Recurrence of Non-Hydropic Sudden Sensorineural Hearing Loss (SSNHL): A Literature Review.","authors":"C Cassandro, P De Luca, M Ralli, F Gioacchini, F Di Berardino, A Albera, R Albera, E Cassandro, A Scarpa","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":54170,"journal":{"name":"Translational Medicine at UniSa","volume":"20 ","pages":"22-27"},"PeriodicalIF":1.5,"publicationDate":"2019-01-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6910150/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37468221","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}