15 results on '"Laino, L."'
Search Results
2. A pigmented acral lesion.
- Author
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Laino, L., Cantisani, C., D. Innocenzi, Bottoni, U., and Calvieri, S.
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LETTERS to the editor , *PIGMENTATION disorders - Abstract
A letter to the editor is presented about the case of a 60-year-old white woman with a pigmented lesion on her third left toe with a duration of one year.
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- 2006
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3. Three Dimensional Printed Surgical Guides: Effect of Time on Dimensional Stability.
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Lo Russo L, Guida L, Zhurakivska K, Troiano G, Di Gioia C, Ercoli C, and Laino L
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- Printing, Three-Dimensional, Dental Implantation, Endosseous, Computer-Aided Design, Surgery, Computer-Assisted
- Abstract
Purpose: To analyze, in vitro, the dimensional stability over time of 3D-printed surgical guides., Materials and Methods: Ten surgical guides, manufactured by digital light processing 3D-printing technology, were scanned immediately after post-processing and then after 5, 10, 15, and 20 days. The corresponding standard tessellation language (STL) files were used for comparison with the reference CAD project. Mean absolute deviation (MAD) of the intaglio surface, axial, and linear deviations of the sleeves' housings were measured. Generalized estimated equations models (α = 0.05) were used to investigate the effect of time., Results: MAD of the teeth intaglio surface showed less variation (minimum: 0.002, maximum: 0.014 mm) than that of the mucosa (minimum: 0.026, maximum: 0.074 mm). Axial variations of the sleeves' housings on the sagittal (minimum: -0.008°, maximum: -0.577°) and frontal plane (minimum: -0.193°, maximum: 0.525°) changed with similar patterns, but opposite trends (decreasing for the former). Linear deviations of center points of the sleeves' housings had a shifting (minimum: -0.074, maximum: 0.02 mm) pattern with a decreasing tendency. Time after processing had a significant effect, either alone or nested with guides volume, on all outcomes of interest, except for MAD of the mucosa intaglio surface (p < 0.001), which was significantly affected only by the time-volume nested effect (p = 0.012)., Conclusions: Within the limitations of the experimental design, postmanufacturing dimensional variations of surgical guides were statistically significant. Although limited, they are an additional source of variability affecting the overall accuracy of computer-guided surgery. As such, they should be addressed by further research., (© 2022 by the American College of Prosthodontists.)
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- 2023
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4. Pre-treatment neutrophil-to-lymphocyte ratio is an independent prognostic factor in head and neck squamous cell carcinoma: Meta-analysis and trial sequential analysis.
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Mariani P, Russo D, Maisto M, Troiano G, Caponio VCA, Annunziata M, and Laino L
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- Humans, Lymphocytes, Prognosis, Squamous Cell Carcinoma of Head and Neck therapy, Head and Neck Neoplasms therapy, Neutrophils
- Abstract
Inflammation seems to play a critical role in the development and progression of different cancers. Neutrophil-to-lymphocyte ratio (NLR) is an easily measurable marker of systemic inflammation. The purpose of this systematic review and meta-analysis was to evaluate the prognostic role of the pre-treatment NLR, in terms of overall survival (OS) and disease-free survival (DFS), in patients with primary head and neck squamous cell carcinoma (HNSCC) treated by surgery alone or followed by chemo/radiotherapy. This systematic review was performed according to the guidelines reported in the Cochrane Handbook and the Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) statement. Meta-analysis of OS and DFS was performed using the inverse of variance test. Fixed-effect models were used on the basis of the presence of heterogeneity. Risk of bias assessment and trial sequential analysis (TSA) were also performed; the quality of the evidence was evaluated via the Grading of Recommendations, Assessment, Development and Evaluation (GRADE) approach. The analysis revealed that a higher value of pre-treatment NLR correlates with a statistically significant decrease of OS (HR, 1.56; 95% CI: [1.35, 1.80]; p < 0.00001) and a lower DFS (HR, 1.64; 95% CI: [1.30, 2.07]; p < 0.0001) in HNSCC patients., (© 2021 The Authors. Journal of Oral Pathology & Medicine published by John Wiley & Sons Ltd.)
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- 2022
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5. Koolen-de Vries syndrome in the first adulthood patient of Southern India ancestry.
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Pascolini G, Gaudioso F, Fadda MT, Laino L, Ferraris A, and Grammatico P
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- Abnormalities, Multiple genetics, Adult, Aging, Chromosome Deletion, Chromosomes, Human, Pair 17 genetics, Chromosomes, Human, Pair 17 ultrastructure, Ethnicity genetics, Face abnormalities, Female, Heart Septal Defects, Atrial genetics, Heart Septal Defects, Atrial surgery, Humans, India, Infant, Newborn, Infant, Premature, Infant, Premature, Diseases genetics, Intellectual Disability genetics, Malocclusion, Angle Class III genetics, Phenotype, Sequence Deletion, Abnormalities, Multiple ethnology, Intellectual Disability ethnology, Nuclear Proteins genetics
- Abstract
Koolen-de Vries syndrome (KdVS, MIM#610443) is a rare malformation condition mainly characterized by cognitive impairment in association with craniofacial and visceral anomalies. The core phenotype is caused by mutations in the chromatin remodeler KANSL1 (MSL1V1, KIAA1267, KAT8 Regulatory NSL Complex Subunit 1, MIM#612452), which maps to 17q21.31 critical genomic region (Koolen et al., Nature Genetics 2012;44:639-641). Considering its molecular basis, KdVS is included in the group of Developmental Disorders of Chromatin Remodeling (DDCRs), also termed chromatinopathies. We describe the first KdVS patient of Southern India ethnicity, harboring the typical de novo 17q21.31 microdeletion, including KANSL1. Observed facial features and congenital anomalies are in line with the already reported KdVS phenotype, suggesting that phenotypic features are consistent across different ethnicities., (© 2020 Wiley Periodicals LLC.)
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- 2021
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6. Early and late implant failure of submerged versus non-submerged implant healing: A systematic review, meta-analysis and trial sequential analysis.
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Troiano G, Lo Russo L, Canullo L, Ciavarella D, Lo Muzio L, and Laino L
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- Humans, Risk Factors, Dental Implantation, Endosseous, Dental Implants, Dental Restoration Failure, Wound Healing
- Abstract
Introduction: The aim of this systematic review was to analyse current evidence regarding differences in early and late implant failure as well as in marginal bone level (MBL) changes between submerged and non-submerged healed dental implants., Methods: PUBMED, SCOPUS, EMBASE and Web of Science databases were searched for prospective randomized and non-randomized controlled studies addressing direct comparison between submerged and non-submerged implant healing, without performing immediate loading. Early and late implant failure (before or after 6 months from implant placement, respectively) together with MBL were the investigated outcomes. Risk of bias assessment was performed using the Cochrane Collaboration Tool for Randomized clinical trials. Meta-analysis was performed and the power of the meta-analytic findings determined by trial sequential analysis (TSA)., Results: Eleven studies met the inclusion criteria and were included in the review. Results of this systematic review revealed a small higher rate (2%) of early implant failure when a non-submerged healing approach is performed. Late implant failure appears not to be different in submerged or non-submerged healing, but the power of evidence, as determined by TSA, is not high. If we consider MBL changes at 1 year from implant load, it seems that non-submerged healing may better preserve marginal bone, although with a small effect size (0.13 mm)., Conclusions: Implants placed with a non-submerged technique have a higher risk (2%) of early failure. The power of the evidence about the effects on MBL is low, but present results seem to favour non-submerged healing, although with a very small effect size., (© 2018 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.)
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- 2018
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7. The potential role of in vivo optical coherence tomography for evaluating oral soft tissue: A systematic review.
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Gentile E, Maio C, Romano A, Laino L, and Lucchese A
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- Humans, Mouth diagnostic imaging, Mouth Diseases diagnostic imaging, Tomography, Optical Coherence
- Abstract
Background: The introduction of optical coherence tomography (OCT) in dentistry enabled the integration of already existing clinical and laboratory investigations in the study of the oral cavity. This systematic review presents an overview of the literature, to evaluate the usefulness of in vivo OCT for diagnosing oral soft tissues lesions, to compare the OCT results with traditional histology, and to identify limitations in prior studies so as to improve OCT applications., Methods: We performed a review of the literature using different search engines (PubMed, ISI Web of Science, and the Cochrane Library) employing MeSH terms such as "optical coherence tomography" and "OCT" in conjunction with other terms. We utilized the Population, Intervention, Comparison, Outcomes, and Study design (PICOS) method to define our study eligibility criteria., Results: Initial results were 3155. In conclusion, there were only 27 studies which met our selection criteria. We decided to allocate the 27 selected items into three groups: healthy mucosa; benign, premalignant, and malignant lesions; and oral manifestations of systemic therapies or pathological conditions., Conclusions: Although the OCT is an easy-to-perform test and it offers an attractive diagnostic and monitoring prospect for soft tissues of the oral cavity, further studies are needed to complete the current knowledge of this imaging technique., (© 2017 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.)
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- 2017
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8. Addition of enamel matrix derivatives to bone substitutes for the treatment of intrabony defects: A systematic review, meta-analysis and trial sequential analysis.
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Troiano G, Laino L, Zhurakivska K, Cicciù M, Lo Muzio L, and Lo Russo L
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- Alveolar Bone Loss surgery, Bone Regeneration, Combined Modality Therapy, Gingival Recession surgery, Humans, Periodontal Attachment Loss surgery, Periodontal Index, Alveolar Bone Loss drug therapy, Bone Substitutes therapeutic use, Dental Enamel Proteins therapeutic use, Gingival Recession drug therapy, Guided Tissue Regeneration, Periodontal methods, Periodontal Attachment Loss drug therapy
- Abstract
Aim: In order to enhance clinical improvement of intrabony defects, the addition of enamel matrix derivatives (EMD) to bone substitues (BS) has been investigated. The aim of this systematic review is to figure out whether such a combination, in comparison to the treatment with BS alone has beneficial effects on the following outcomes: clinical attachment level (CAL) gain, probing depth (PD) reduction and recession (REC)., Methods: Electronic databases (PUBMED, SCOPUS, EBSCO Host Research Databases and Web of Knowledge) were searched for randomized controlled trials in humans addressing the use of a combination of BS and EMD versus a control group with BS alone for the treatment of intrabony defects, with a minimum of 6 months of follow-up; meta-analysis and trial sequential analysis were then performed., Results: From a total of 1,197 records screened by title and abstract, nine studies were read full-text and five out of them included in the meta-analysis. No significant differences have been demonstrated both for CAL gain, PD reduction and REC between test and control groups., Conclusions: In the treatment of intrabony defects, the addition of EMD to BS seems to be not beneficial in terms of CAL gain, PD reduction and REC changes. However, such results should be considered with caution because of the small number of studies included in the meta-analysis and their heterogeneity., (© 2017 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.)
- Published
- 2017
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9. The potential role of in vivo reflectance confocal microscopy for evaluating oral cavity lesions: a systematic review.
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Lucchese A, Gentile E, Romano A, Maio C, Laino L, and Serpico R
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- Autoimmune Diseases diagnosis, Autoimmune Diseases pathology, Humans, Microscopy, Confocal instrumentation, Mouth Diseases diagnosis, Mouth Mucosa diagnostic imaging, Mouth Mucosa pathology, Mouth Neoplasms diagnostic imaging, Mouth Neoplasms pathology, Precancerous Conditions diagnosis, Precancerous Conditions pathology, Microscopy, Confocal methods, Mouth Diseases diagnostic imaging, Mouth Diseases pathology
- Abstract
Background: Since the early 2000s, several studies have examined the application of reflectance confocal microscopy (RCM) to the oral cavity. This review gives an overview of the literature on reflectance confocal microscopy analysis of the oral cavity in vivo and identifies flaws in the studies, providing guidance to improve reflectance confocal microscopy applications and inform the design of future studies., Methods: The PubMed, ISI, Scopus, and Cochrane Library databases were searched for publications on RCM using the terms 'reflectance confocal microscopy' in combination with 'mouth' and other terms related to the topic of interest., Results: The search gave 617 results. Seventeen studies were included in our final analysis. We decided to organize the selected articles according to four topics: healthy mucosa, autoimmune diseases, cancer and precancerous lesions, and hard dental tissues., Conclusion: Although reflectance confocal microscopy is promising for diagnosing and monitoring oral pathology, it has shortcomings and there are still too few publications on this topic. Further studies are needed to increase the quantity and quality of the results, to translate research into clinical practice., (© 2016 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.)
- Published
- 2016
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10. Axial skeletogenesis in human autosomal aneuploidies: A radiographic study of 145 second trimester fetuses.
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Castori M, Servadei F, Laino L, Pascolini G, Fabbri R, Cifani AE, Sforzolini GS, Silvestri E, and Grammatico P
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- Abortion, Eugenic, Autopsy, Bone and Bones diagnostic imaging, Bone and Bones metabolism, Chromosome Disorders diagnostic imaging, Chromosome Disorders genetics, Chromosome Disorders pathology, Chromosomes, Human, Pair 13 genetics, Chromosomes, Human, Pair 18 genetics, Down Syndrome diagnostic imaging, Down Syndrome genetics, Down Syndrome pathology, Female, Fetus, Gestational Age, Humans, Male, Osteogenesis genetics, Pregnancy, Pregnancy Trimester, Second, Prenatal Diagnosis, Retrospective Studies, Trisomy genetics, Trisomy pathology, Trisomy 13 Syndrome, Trisomy 18 Syndrome, Aneuploidy, Bone and Bones abnormalities, Chromosome Disorders diagnosis, Down Syndrome diagnosis, Trisomy diagnosis
- Abstract
Autosomal aneuploidies associate with multiple minor skeletal defects, which, in fetuses, are best appreciated post-mortem after specific anatomic preparations. The present study was aimed to define patterns of skeletal anomalies in autosomal aneuploidies at standard radiology in second trimester fetuses by comparing findings in and among genotypes and gestational ages. Aneuploid fetuses were selected for availability of radiographs of various axial and non-axial structures, mainly homeotic transformations, vertebral clefts, vertebral segmentation and ossification defects, absent/hypoplastic nasal bone, premature talar calcifications, and selected appendicular anomalies. Eighty six fetuses with trisomy 21, 39 with trisomy 18, eight with trisomy 13, six with triploidy, and six with rare autosomal aneuploidies were identified, 75.2% showing an abnormal costo-vertebral pattern, mostly cervical ribs, absence of the 12th thoracic ribs and posterior homeotic change. Clefting was observed along the entire spine, especially sagittal lumbar clefts, and coronal thoracic clefts. Four different types of vertebral clefting were identified, including type 1 (butterfly), type 2 (incomplete inferior), type 3 (incomplete superior), and type 4 (complete). Attenuation of clefting by gestational age was observed in trisomy 21 and 18. These findings define more clearly the pattern of perturbed morphogenesis in aneuploidy as a type of amplified developmental instability with pleiotropic effects on skeletogenesis., (© 2015 Wiley Periodicals, Inc.)
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- 2016
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11. Longitudinal hormonal evaluation in a patient with disorder of sexual development, 46,XY karyotype and one NR5A1 mutation.
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Pedace L, Laino L, Preziosi N, Valentini MS, Scommegna S, Rapone AM, Guarino N, Boscherini B, De Bernardo C, Marrocco G, Majore S, and Grammatico P
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- Child, DNA Mutational Analysis, Disorder of Sex Development, 46,XY diagnosis, Genitalia, Male abnormalities, Gonadal Dysgenesis, 46,XY diagnosis, Gonadal Dysgenesis, 46,XY genetics, Gonadal Dysgenesis, 46,XY pathology, Humans, Longitudinal Studies, Male, Phenotype, Disorder of Sex Development, 46,XY blood, Disorder of Sex Development, 46,XY genetics, Hormones blood, Mutation, Steroidogenic Factor 1 genetics
- Abstract
Steroidogenic factor 1 (encoded by the NR5A1 gene) is a critical regulator of reproduction, controlling transcription of key genes involved in sexual dimorphism. To date, NR5A1 variants have been found in individuals with a 46,XY karyotype and gonadal dysgenesis, as well as with a wide spectrum of genital anomalies and, in some patients, with adrenal insufficiency. We describe evolution of gonadal function, from the neonatal period to puberty, in a patient with a 46,XY karyotype, a disorder of sexual development, and a mutation (c.691_699dupCTGCAGCTG) in the NR5A1 gene. The patient, ascertained at birth due to ambiguous genitalia, showed normal values of plasma testosterone in the late neonatal period. Evaluation of the hormonal profile over time indicated severe tubular testicular hypofunction suggestive for a 46,XY disorder of gonadal development. A comprehensive review of published reports of 46,XY and disordered sexual development related to the NR5A1 gene confirmed the clinical and hormonal variability in patients with NR5A1 mutations. Analysis of multiple data allowed us to define the most common features associated with NR5A1 mutations. We further confirmed the indication to perform NR5A1 screening in patients with 46,XY karyotype and disordered sexual development even when Müllerian structures appear to be absent and plasma testosterone levels are within the normal range for age., (© 2014 Wiley Periodicals, Inc.)
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- 2014
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12. Can video thermography improve differential diagnosis and therapy between basal cell carcinoma and actinic keratosis?
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Di Carlo A, Elia F, Desiderio F, Catricalà C, Solivetti FM, and Laino L
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- Aged, Carcinoma, Basal Cell pathology, Carcinoma, Basal Cell physiopathology, Dermoscopy, Diagnosis, Differential, Female, Fever physiopathology, Humans, Hypothermia physiopathology, Keratosis, Actinic pathology, Keratosis, Actinic physiopathology, Male, Middle Aged, Predictive Value of Tests, Skin pathology, Skin Neoplasms pathology, Skin Neoplasms physiopathology, Body Temperature, Carcinoma, Basal Cell diagnosis, Fever diagnosis, Hypothermia diagnosis, Keratosis, Actinic diagnosis, Skin Neoplasms diagnosis, Thermography, Video Recording
- Abstract
Various noninvasive techniques (dermoscopy, confocal microscopy, etc.) have been introduced to help the clinical diagnosis in nonmelanoma skin cancer. Among them, the high definition video thermographic technique (VTG) has recently been proposed. The aim of this study is to define the VTG patterns, respectively of actinic keratosis (AK) and basal cell carcinoma (BCC), and to compare these data with them of dermoscopy. The study included 36 patients with a total number of 135 lesions who underwent clinical, VTG, and dermoscopic examination. The VTG showed the presence of a hyperthermic pattern in all the cases of AK, while in the case of the BCC, the pattern was hypothermic. Dermoscopy also showed distinct pattern for AK and for BCC, but in 22% of them the data were not conclusive. Our study permits us to define two specific VTG patterns, BCC and AK respectively., (© 2014 Wiley Periodicals, Inc.)
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- 2014
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13. Early healing of the alveolar process after tooth extraction: an experimental study in the beagle dog.
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Discepoli N, Vignoletti F, Laino L, de Sanctis M, Muñoz F, and Sanz M
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- Analysis of Variance, Animals, Dogs, Time Factors, Alveolar Bone Loss etiology, Alveolar Process physiology, Bone Remodeling physiology, Tooth Extraction adverse effects, Tooth Socket physiology, Wound Healing physiology
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Aim: To describe the early healing events in the alveolar socket during the first 8 weeks of spontaneous healing after tooth extraction., Materials and Methods: 16 adult beagle dogs were selected and five healing periods were analysed (4 h, 1 week, 2 weeks, 4 weeks, 8 weeks). Mandibular premolars were extracted and each socket corresponding to the mesial root was left to heal undisturbed. In each healing period, three animals were euthanatized, each providing four study sites. Healing was assessed by descriptive histology and by histometric analysis using as landmarks: the vertical distance between buccal and lingual crest (B'L') and the width of buccal and lingual walls at three different levels. Differences between means for each variable for each healing period were compared (ANOVA; p < 0.05)., Results: B'L' at baseline was 0.45 (0.18) mm and decreased during the healing period to a final value of 0.18 (0.08) mm. The lingual width (Lw) remains almost unchanged while the buccal width (Bw) at 1 (Bw1) and 2 (Bw2) mm was reduced in about 40% of its initial value., Conclusions: Minor vertical bone reduction in both the buccal and lingual socket walls were observed. A marked horizontal reduction of the buccal bone wall was observed mostly in its coronal aspect., (© 2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.)
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- 2013
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14. Elsahy-Waters syndrome: Evidence for autosomal recessive inheritance.
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Castori M, Cascone P, Valiante M, Laino L, Iannetti G, Hennekam RC, and Grammatico P
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- Abnormalities, Multiple diagnostic imaging, Abnormalities, Multiple pathology, Adolescent, Adult, Child, Preschool, Female, Humans, Infant, Newborn, Male, Middle Aged, Pregnancy, Radiography, Skull diagnostic imaging, Skull pathology, Syndrome, Abnormalities, Multiple genetics, Genes, Recessive genetics, Inheritance Patterns genetics
- Abstract
Elsahy-Waters or branchioskeletogenital syndrome is a rare MCA/MR syndrome characterized by moderate mental retardation, hypospadias and characteristic craniofacial morphology, which includes brachycephaly, facial asymmetry, exotropia, hypertelorism/telechantus, broad nose, concave nasal ridge, underdeveloped midface, prognathism, and radicular dentin dysplasia. Here we report on a 44-year-old woman and her 45-year-old brother, born to consanguineous parents, who show a striking resemblance to the earlier described patients. The hitherto reported patients were male and in one pedigree parents were consanguineous. The present report of an affected woman and her brother, born to consanguineous parents, supports autosomal recessive inheritance of this condition. We provide a short review of all previously reported patients with Elsahy-Waters syndrome and related entities., (© 2010 Wiley-Liss, Inc.)
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- 2010
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15. Darier disease, multiple bone cysts, and aniridia due to double de novo heterozygous mutations in ATP2A2 and PAX6.
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Castori M, Barboni L, Duncan PJ, Paradisi M, Laino L, De Bernardo C, Robinson DO, and Grammatico P
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- Adolescent, Adult, Aniridia complications, Bone Cysts complications, Bone Cysts diagnostic imaging, Child, Darier Disease complications, Female, Humans, Infant, Male, PAX6 Transcription Factor, Radiography, Young Adult, Aniridia genetics, Bone Cysts genetics, Darier Disease genetics, Eye Proteins genetics, Heterozygote, Homeodomain Proteins genetics, Mutation genetics, Paired Box Transcription Factors genetics, Repressor Proteins genetics, Sarcoplasmic Reticulum Calcium-Transporting ATPases genetics
- Abstract
Darier disease (DD) is an autosomal dominant genodermatosis caused by mutations in ATP2A2 and characterized by multiple warty papules coalescing in seborrheic areas and specific histological skin changes. Rare patients are described with variable bone involvement, but this association has never been sufficiently emphasized. Aniridia is a developmental disorder of the eye due to heterozygous mutations in PAX6. DD and aniridia are Mendelian traits mapping on independent loci and have never been reported in association. Here, we describe a 14-year-old girl showing the unique combination of DD, multiple bone cysts, and bilateral aniridia. Molecular investigations demonstrated that such a complex phenotype is due to double de novo heterozygous mutations in ATP2A2 and PAX6. Review of the literature indicates that, in DD, bone cysts are true developmental abnormalities of the skeleton. This finding suggests a role for ATP2A2 in bone biology. More systematic studies are expected in order to estimate the true prevalence of bone cysts in DD and the relationship between skeletal changes and ATP2A2 perturbation., (2009 Wiley-Liss, Inc.)
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- 2009
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