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Incidental detection of benign metastasizing leiomyoma in asymptomatic female. 无症状女性良性转移性平滑肌瘤的偶然发现。
IF 0.9 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2023-01-01 DOI: 10.25259/JCIS_37_2023
Hannah E Zazulak, Meghan Single, Timothy O'Herron, Joel P Thompson

Benign metastasizing leiomyoma (BML) is a rare finding of histologically benign smooth muscle tumors in extrauterine locations, most commonly the lungs. We report a case of BML found incidentally on pre-operative imaging in a 42-year-old patient. BML is found in premenopausal women with a history of leiomyoma and, often, hysterectomy. As in our case, the metastatic pulmonary nodules are not hypermetabolic on 18F-fluorodeoxyglucose Positron emission tomography/computed tomography. BML may be clinically malignant or asymptomatic. Since the imaging appearance of BML simulates metastatic disease of more malignant etiology, awareness of its multimodality imaging appearance and presentation can aid in diagnosis.

良性转移性平滑肌瘤(BML)是一种罕见的子宫外部位良性平滑肌肿瘤,最常见于肺部。我们报告一个42岁的患者在术前影像学上偶然发现的BML病例。BML见于有平滑肌瘤和子宫切除术史的绝经前妇女。在本病例中,转移性肺结节在18f -氟脱氧葡萄糖正电子发射断层扫描/计算机断层扫描上没有高代谢。BML在临床上可能是恶性的或无症状的。由于BML的影像学表现类似于恶性病因的转移性疾病,因此了解其多模态影像学表现和表现有助于诊断。
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引用次数: 1
Survival and clinical success of endovascular intervention in patients with Budd-Chiari syndrome: A systematic review. Budd-Chiari综合征患者血管内介入治疗的生存和临床成功:一项系统综述。
IF 0.9 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2023-01-01 DOI: 10.25259/JCIS_130_2022
Gauri Mukhiya, Dechao Jiao, Xinwei Han, Xueliang Zhou, Gaurab Pokhrel

Budd-Chiari syndrome is a complex clinical disorder of hepatic venous outflow obstruction, originating from the accessory hepatic vein (HV), large HV, and suprahepatic inferior vena cava (IVC). This disorder includes both HV and IVC obstructions and hepatopathy. This study aimed to conduct a systematic review of the survival rate and clinical success of different types of endovascular treatments for Budd-Chiari syndrome (BCS). All participant studies were retrieved from four databases and selected according to the eligibility criteria for systematic review of patients with BCS. The survival rate, clinical success of endovascular treatments in BCS, and survival rates at 1 and 5 years of publication year were calculated accordingly. A total of 3398 patients underwent an endovascular operation; among them, 93.6% showed clinical improvement after initial endovascular treatment. The median clinical success rates for recanalization, transjugular intrahepatic portosystemic shunt (TIPS), and combined procedures were 51%, 17.50%, and 52.50%, respectively. The median survival rates at 1 and 5 years were 51% and 51% for recanalization, 17.50% and 16% for TIPS, and 52.50% and 49.50% for combined treatment, respectively. Based on the year of publication, the median survival rates at 1 and 5 years were 23.50% and 22.50% before 2000, 41% and 41% in 2000‒2005, 35% and 35% in 2006‒2010, 51% and 48.50% in 2010‒2015, and 56% and 55.50% after 2015, respectively. Our findings indicate that the median survival rate at 1 and 5 years of recanalization treatment is higher than that of TIPS treatment, and recanalization provides better clinical improvement. The publication year findings strongly suggest progressive improvements in interventional endovascular therapy for BCS. Thus, interventional therapy restoring the physiologic hepatic venous outflow of the liver can be considered as the treatment of choice for patients with BCS which is a physiological modification procedure.

Budd-Chiari综合征是一种复杂的肝静脉流出梗阻的临床疾病,起源于肝副静脉(HV)、大静脉(HV)和肝上下腔静脉(IVC)。这种疾病包括肝炎和下腔静脉阻塞和肝病。本研究旨在对不同类型血管内治疗Budd-Chiari综合征(BCS)的生存率和临床成功率进行系统评价。所有参与研究均从四个数据库中检索,并根据BCS患者系统评价的资格标准进行选择。计算BCS患者的生存率、血管内治疗的临床成功率以及发表后1年和5年的生存率。共有3398例患者接受了血管内手术;其中93.6%的患者经血管内治疗后临床好转。再通、经颈静脉肝内门体分流术(TIPS)和联合手术的临床成功率中位数分别为51%、17.50%和52.50%。再通组1年和5年的中位生存率分别为51%和51%,TIPS组为17.50%和16%,联合治疗组为52.50%和49.50%。以发表年份为准,2000年前1年和5年的中位生存率分别为23.50%和22.50%,2000 - 2005年为41%和41%,2006-2010年为35%和35%,2010-2015年为51%和48.50%,2015年后为56%和55.50%。我们的研究结果表明,再通治疗1年和5年的中位生存率高于TIPS治疗,再通治疗可提供更好的临床改善。发表年的研究结果强烈表明介入血管内治疗BCS的进展性改进。因此,恢复肝脏生理性肝静脉流出的介入治疗可以被认为是BCS患者的治疗选择,这是一种生理修饰过程。
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引用次数: 1
Lemmel syndrome, a rare cause of obstructive jaundice by periampullary duodenal diverticulum: Case report and review of the literature. 壶腹周围十二指肠憩室梗阻性黄疸的罕见病因Lemmel综合征:病例报告及文献复习。
IF 0.9 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2023-01-01 DOI: 10.25259/JCIS_9_2023
Massupa Krisem, Pornrujee Hirunpat, Nuttapat Tungtrongchitr

Lemmel syndrome is a pancreaticoduodenal disease caused by compression of the mid or distal common bile duct by a periampullary diverticulum. This condition should be considered a rare complication of a duodenal diverticulum and an unusual cause of obstructive jaundice. Because of its infrequent occurrence and non-specific clinical presentation, Lemmel syndrome can mimic other conditions. We herein report the clinical and imaging findings (computed tomography, magnetic resonance imaging) of a patient who presented with intermittent abdominal pain and jaundice. Large air-filled outpouching lesions of the duodenum compressed the biliary duct, resulting in upstream biliary ductal dilatation that led to the diagnosis of Lemmel syndrome.

Lemmel综合征是一种胰十二指肠疾病,由壶腹周围憩室压迫中段或远段胆总管引起。这种情况应被认为是十二指肠憩室的罕见并发症和梗阻性黄疸的不寻常原因。由于其罕见的发生和非特异性的临床表现,Lemmel综合征可以模仿其他疾病。我们在此报告的临床和影像学结果(计算机断层扫描,磁共振成像)的病人谁提出间歇性腹痛和黄疸。十二指肠大量充满空气的突出病变压迫胆管,导致胆管上游扩张,从而诊断为Lemmel综合征。
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引用次数: 0
Transradial versus transfemoral arterial access in Yttrium-90 microspheres radioembolization for hepatocellular carcinoma 经桡动脉与经股动脉在肝细胞癌钇-90微球放射栓塞治疗中的应用
IF 0.9 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2022-05-12 DOI: 10.25259/JCIS_213_2021
Abheek Ghosh, Jian Zhang, N. Akhter
OBJECTIVE Transradial access has become more popular in body intervention procedures but has not been ubiquitously adapted. This study assesses the efficacy of this approach in Yttrium-90 labeled microspheres radioembolization. To compare transradial to transfemoral access in hepatocellular carcinoma patients who underwent Yttrium-90 radioembolization. MATERIALS AND METHODS A total of 244 hepatocellular carcinoma patients underwent 337 radioembolization procedures at our institute from May 2014 to May 2020. The transradial access-group included 188 patients (252 procedures) while the transfemoral access group had 63 patients (85 procedures). The recovery time, fluoroscopy time, contrast volume, peak radiation dose, and equipment cost for each procedure were all reviewed to evaluate for statistical differences between the two groups. RESULTS The transradial cohort recorded a significantly shorter (P < 0.01) mean recovery time (from the end of the procedure to discharge) and had a significantly shorter (P < 0.05) use of contrast volume versus the transfemoral group. In addition, the radiation dose and fluoroscopy time were lower in the transradial subset, although not statistically different. Furthermore, the overall cost for procedural equipment was significantly less (P < 0.01) in the transradial cohort than in the transfemoral. No major complications were reported in the transradial group, while one pseudoaneurysm was noted in the transfemoral group. CONCLUSION With respect to many pertinent parameters, transradial access was evaluated as being more advantageous than transfemoral access. The results of this study suggest that transradial access should be considered more often, whenever feasible, as an option in the Yttrium-90 treatment of hepatocellular carcinoma patients.
目的经桡骨通路在身体介入手术中越来越流行,但并没有被普遍采用。本研究评估了该方法在钇-90标记微球放射栓塞中的疗效。目的:比较经桡动脉与经股动脉通路在肝细胞癌患者行钇-90放射栓塞的疗效。材料与方法2014年5月至2020年5月,共有244例肝癌患者在我所接受了337次放射栓塞手术。经桡动脉入路组包括188例患者(252例手术),而经股骨入路组有63例患者(85例手术)。对每一种手术的恢复时间、透视时间、造影剂体积、峰值辐射剂量和设备成本进行评估,以评估两组之间的统计学差异。结果:与经股动脉组相比,经桡动脉组的平均恢复时间(从手术结束到出院)显著缩短(P < 0.01),造影剂用量显著缩短(P < 0.05)。此外,放射亚群的放射剂量和透视时间较低,但无统计学差异。此外,经桡动脉组的手术设备总成本明显低于经股骨组(P < 0.01)。经桡动脉组无重大并发症,经股动脉组有一例假性动脉瘤。结论在许多相关参数方面,经桡动脉入路优于经股动脉入路。本研究的结果表明,在肝细胞癌患者的钇-90治疗中,只要可行,应更多地考虑经桡动脉通路作为一种选择。
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引用次数: 2
Plain X-ray findings of post sleeve gastrectomy gastric leak 套筒胃切除术后胃漏的x线平片表现
IF 0.9 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2022-05-12 DOI: 10.25259/JCIS_6_2022
Sultan R. Alharbi
Gastric leak following sleeve gastrectomy (SG) is a rare but significant cause of morbidity and mortality. A high clinical index of suspicion is the most sensitive approach to detect gastric leaks. Computed tomography (CT) is the gold standard diagnostic technique, although it might not be performed due to unavailability, and the inability to image superobese patients due to limited CT gantry space. Early detection and management are critical for attaining a better prognosis. The following pictorial review discusses the various plain X-ray radiographic findings that indicate a gastric leak. These findings may be overlooked, however, they remain valuable in patients with clinically suspected gastric leaks. This pictorial review illustrates the spectrum of findings related to post-SG gastric leak encountered in plain X-ray radiography.
摘要袖式胃切除术后胃漏是一种罕见但重要的致死率原因。临床怀疑指数高是检测胃漏最灵敏的方法。计算机断层扫描(CT)是金标准诊断技术,尽管由于缺乏可用性,以及由于CT机架空间有限而无法对超肥胖患者进行成像,但它可能无法进行。早期发现和治疗对于获得更好的预后至关重要。下面的图片回顾讨论了显示胃漏的各种x线平片表现。这些发现可能被忽视,然而,它们对临床怀疑胃漏的患者仍然有价值。本图片回顾说明了在x线平片上与sg后胃漏相关的发现谱。
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引用次数: 1
Imaging findings and interventional management of deep venous thrombosis 深静脉血栓形成的影像学表现及介入治疗
IF 0.9 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2022-05-12 DOI: 10.25259/JCIS_221_2021
H. Hindi, G. Dongmo, Alyssa Goodwin, S. Jones, Kristian Loveridge
Deep venous thrombosis (DVT) is a subtype of venous thromboembolism. Lower extremity DVT affects about 1-2% of hospitalized patients. If not managed properly, these thrombi can embolize, causing further complications. Thrombosis risk factors include vascular endothelial injury, venous stasis, and hypercoagulability states. This triad is also known as Virchow’s triad. Although clinical features of lower extremity DVT are nonspecific and many patients are asymptomatic, physicians should maintain a high index of suspicion in patients presenting with leg swelling, pain, warmth, and erythema. Several diagnostic approaches for suspected first DVT have been proposed, and management depends on multiple factors such as location, duration of symptoms, cause of the thrombosis, and recurrence rate.
深静脉血栓形成(DVT)是静脉血栓栓塞的一种亚型。下肢深静脉血栓约占住院患者的1-2%。如果处理不当,这些血栓可能会栓塞,导致进一步的并发症。血栓形成的危险因素包括血管内皮损伤、静脉淤滞和高凝状态。这个三和弦也被称为维尔肖三和弦。尽管下肢深静脉血栓的临床特征是非特异性的,许多患者无症状,但对于出现腿部肿胀、疼痛、发热和红斑的患者,医生应保持高度的怀疑。对于疑似首次深静脉血栓的几种诊断方法已经被提出,治疗取决于多种因素,如位置、症状持续时间、血栓形成的原因和复发率。
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引用次数: 0
Bilateral oligodendroglial hamartomas: A rare cause of drug-resistant epilepsy in a pediatric patient 双侧少突胶质错构瘤:小儿患者耐药癫痫的罕见病因
IF 0.9 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2022-05-05 DOI: 10.25259/JCIS_197_2021
Havisha Munjal, D. Mistry, J. Almast, S. Ellika
Intractable or drug-resistant seizures in pediatric patients are often secondary to cortical malformations, hamartomas, or mass lesions. Various subtypes of intracerebral hamartomas, associated with seizure disorders, have been described. In this report, we describe a subtype of intracerebral hamartoma associated with intractable epilepsy in a 10-year-old patient. Initial MR imaging demonstrated a mildly expansile, T2/FLAIR hyperintense, T1 isointense, nonenhancing lesion with blurring of the gray-white junction in the left amygdala. Surgical resection was performed, and pathology confirmed oligodendroglial hamartoma. Patient’s seizures recurred after a two-year interval with imaging demonstrating a similar lesion in the right amygdala which in retrospect was also seen on multiple imaging studies. This case report demonstrates the importance of recognizing oligodendroglial hamartomas as a cause of intractable seizures given the imaging findings, distinguishing it from ganglioglioma, dysembryoplastic neuroepithelial tumor, and oligodendroglioma, and the importance of closely looking/searching for contralateral lesions, which has important therapeutic and prognostic implications.
顽固性或耐药性癫痫患儿通常继发于皮质畸形、错构瘤或肿块病变。不同亚型的脑内错构瘤,与癫痫相关的疾病,已被描述。在这篇报告中,我们描述了一个10岁的顽固性癫痫患者的脑内错构瘤亚型。最初的MR成像显示轻度扩张,T2/FLAIR高信号,T1等信号,左侧杏仁核灰白色交界处模糊,无强化病变。手术切除,病理证实少突胶质错构瘤。患者癫痫发作间隔两年后复发,影像学显示右侧杏仁核有类似的病变,回想起来在多次影像学检查中也发现了类似的病变。本病例报告表明,鉴于影像学表现,将少突胶质错构瘤与神经节胶质瘤、胚胎发育异常神经上皮肿瘤和少突胶质胶质瘤区分开来,以及密切观察/寻找对侧病变的重要性,这对治疗和预后具有重要意义。
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引用次数: 0
Morphometric anlaysis of mandibular coronoid, condyle and sigmoid shape using panoromic view for personal identification in south Indian population 南印度人群下颌冠状、髁状和乙状骨形态的全景分析与个人识别
IF 0.9 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2022-05-05 DOI: 10.25259/JCIS_27_2022
Manpreet Manoj, Leeba Mathew, S. Natarajan, Shweta Yellapurkar, S. Shetty, Ceena Denny, S. Dahal
Objective The shape of the condyle, coronoid, and the intervening sigmoid notch is unique due to attachments and direction of pull of temporalis muscle, different chewing habits, hormones, etc. So morphometric variation of these mandibular landmarks can be used in individual identification. Material And Methods The study was carried out on 500 panoramic view images. Visual tracing assisted assessment of thousand sides (left and right) was done. Sexual dimorphism of left and right mandibular ramus parts (sigmoid notch bordered by coronoid and condylar process). The shape of coronoid process, condyle, and sigmoid notch were interpreted. Results The most prevalent shape of sigmoid notch was wide variant (41.2%), condyle was convex type (50%) and coronoid was round (53.4%). Condyle and coronoid showed asymmetry between right and left with p-value 0.001 and 0.019, respectively. This study has illustrated that triangular-shaped coronoid was more in females (p-value 0.012). Conclusion Sexual dimorphism is observed in the shape of the mandible due to masticatory activity at the point of insertion of temporalis muscle, biting force, hormones, and various genetic reasons. The results have exemplified that the morphometric variation of condyle, coronoid and sigmoid notch can be used as a tool for personal identification.
目的髁状突、冠状突及其间的乙状突切迹由于颞肌的附着、牵引方向、咀嚼习惯、激素等因素的不同而具有独特的形状。所以这些下颌标志的形态变化可以用于个体识别。材料与方法采用500张全景图像进行研究。视觉追踪辅助评价了左右两侧。左右下颌骨分支(乙状切迹与冠状突和髁突接壤)的两性异形。对冠突、髁突和乙状骨切迹的形状进行了解释。结果乙状结肠切迹以宽型为主(41.2%),髁突以凸型为主(50%),冠突以圆形为主(53.4%)。髁突和冠突表现为左右不对称,p值分别为0.001和0.019。本研究表明,女性冠状面多为三角形(p值为0.012)。结论颞肌止点处的咀嚼活动、咬合力、激素及各种遗传因素均可引起下颌骨的两性异形。结果表明,髁状突、冠状突和乙状突切迹的形态变化可以作为个人识别的工具。
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引用次数: 0
Computed tomography imaging findings of nivolumab-induced thyroid dysfunction 尼伏单抗致甲状腺功能障碍的计算机断层成像表现
IF 0.9 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2022-05-02 DOI: 10.25259/JCIS_194_2021
Tatsuya Oki, Akitoshi Inoue, Y. Nagatani, Maya Oki, Yoshiyuki Watanabe
The thyroid gland is most frequently involved in immune-related adverse events (irAEs) by nivolumab. We reviewed the thyroid function and thyroid gland volume and volume change ratio between baseline and follow-up CT (volume follow-up/volume baseline) in 24 patients treated with nivolumab for lung cancer and renal cell carcinoma. Among them, four (16.7%) demonstrated nivolumab-induced thyroid dysfunction that shows either hypothyroidism or hyperthyroidism. Three and one cases were treated with nivolumab for lung cancer and renal cell carcinoma, respectively. Two patients with hypothyroidism (cases 1 and 2) showed reduced thyroid volume (volume change ratio: 0.80 and 0.84) on computed tomography (CT) images. Besides, remarkably diminished CT attenuation of the thyroid gland was observed in a patient with hypothyroidism (case 2). One of the two patients with hyperthyroidism showed increased thyroid volume (volume change ratio: 1.32) (case 3), whereas no difference in the thyroid gland volume was observed between the previous and follow-up CT in another patient with hyperthyroidism (case 4). Thyroid volume change ratio >0.1 was observed even in 6 of 20 (30%) patients without thyroid dysfunction. Considering the wide use of nivolumab in cancer treatment, radiologists should be aware that changes in the thyroid volume and attenuation on CT are associated with thyroid dysfunction caused by nivolumab, as well as thyroid volume may change even in patients with normal thyroid function during nivolumab therapy.
甲状腺是纳武单抗最常涉及的免疫相关不良事件(irAEs)。我们回顾了24例接受纳武单抗治疗的肺癌和肾细胞癌患者的甲状腺功能和甲状腺体积和体积变化比基线和随访CT(体积随访/体积基线)。其中4例(16.7%)表现为尼武单抗诱导的甲状腺功能障碍,表现为甲状腺功能减退或甲状腺功能亢进。纳武单抗治疗肺癌和肾细胞癌分别为3例和1例。2例甲状腺功能减退患者(例1和例2)在CT上表现为甲状腺体积缩小(体积变化比分别为0.80和0.84)。另外,1例甲状腺功能减退患者(病例2)的甲状腺CT减影明显减弱。2例甲亢患者中1例甲状腺体积增大(体积变化率为1.32)(病例3),而另1例甲亢患者(病例4)的甲状腺体积前后CT无差异。20例无甲状腺功能障碍患者中6例(30%)甲状腺体积变化率大于0.1。考虑到纳武单抗在癌症治疗中的广泛应用,放射科医生应该意识到,甲状腺体积的变化和CT上的衰减与纳武单抗引起的甲状腺功能障碍有关,即使甲状腺功能正常的患者在纳武单抗治疗期间,甲状腺体积也可能发生变化。
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引用次数: 0
Isolated congenital absence of bilateral femur: A rare case report with antenatal diagnosis and postnatal follow-up 孤立的先天性双侧股骨缺失:一例罕见的产前诊断和产后随访报告
IF 0.9 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2022-05-02 DOI: 10.25259/JCIS_219_2021
A. Kapoor, Tushar Kapoor, Aakaar Kapoor, Apurva Kapoor, R. Kapoor, Veronica Arora, Deepak Mehar
We report a rare case of isolated congenital absence of the bilateral femur diagnosed antenatally in an 18-19 weeks fetus on a level II scan. The bilateral femur bones were not visualized with normal bilateral tibia and fibula. The fetus was followed with a routine growth scan at 32-33 weeks along with a fetal MRI, which showed similar findings. The antenatal findings were confirmed clinically as well as with a postnatal follow-up X-Ray (infantogram) of the baby. Trio whole-exome sequencing was performed for the child as well as both the parents, which did not reveal any clinically significant variant that could explain the patient’s phenotype.
我们报告一例罕见的孤立先天性双侧股骨缺位在产前诊断18-19周胎儿的II级扫描。双侧股骨未见正常双侧胫骨和腓骨。在32-33周时,对胎儿进行了常规生长扫描,并进行了胎儿核磁共振成像,结果显示了类似的结果。产前检查结果经临床证实,并与产后随访x线(婴儿图)的婴儿。对孩子和父母进行了三人全外显子组测序,没有发现任何可以解释患者表型的临床显著变异。
{"title":"Isolated congenital absence of bilateral femur: A rare case report with antenatal diagnosis and postnatal follow-up","authors":"A. Kapoor, Tushar Kapoor, Aakaar Kapoor, Apurva Kapoor, R. Kapoor, Veronica Arora, Deepak Mehar","doi":"10.25259/JCIS_219_2021","DOIUrl":"https://doi.org/10.25259/JCIS_219_2021","url":null,"abstract":"We report a rare case of isolated congenital absence of the bilateral femur diagnosed antenatally in an 18-19 weeks fetus on a level II scan. The bilateral femur bones were not visualized with normal bilateral tibia and fibula. The fetus was followed with a routine growth scan at 32-33 weeks along with a fetal MRI, which showed similar findings. The antenatal findings were confirmed clinically as well as with a postnatal follow-up X-Ray (infantogram) of the baby. Trio whole-exome sequencing was performed for the child as well as both the parents, which did not reveal any clinically significant variant that could explain the patient’s phenotype.","PeriodicalId":15512,"journal":{"name":"Journal of Clinical Imaging Science","volume":"32 1","pages":""},"PeriodicalIF":0.9,"publicationDate":"2022-05-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78894310","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}
引用次数: 0
期刊
Journal of Clinical Imaging Science
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