Syndrome Diagnosed(診斷出的綜合症)到底是什麼？
Syndrome Diagnosed 診斷出的綜合症 - We report a case of a variant presentation of Wellens’ syndrome diagnosed after the resolution of a transient left bundle branch block (LBBB). [1] We present the case of a newborn with this syndrome diagnosed by genetic analysis in a secondary care hospital. [2] Here, we report five cases of 5p‐ syndrome diagnosed by invasive prenatal diagnosis. [3] Case 2 was a 28-year-old man who had untreated Klinefelter’s syndrome diagnosed in his childhood and a 2-year history of hypertension and hypokalemia. [4]我們報告了一例在短暫性左束支傳導阻滯 (LBBB) 消退後診斷為 Wellens 綜合徵的變異表現的病例。 [1] 我們介紹了在二級保健醫院通過基因分析診斷出患有這種綜合徵的新生兒病例。 [2] 在這裡，我們報告了 5 例通過侵入性產前診斷診斷出的 5p 綜合徵。 [3] 病例 2 是一名 28 歲的男性，他在童年時期被診斷出患有未經治療的克蘭費爾特綜合徵，並且有 2 年的高血壓和低鉀血症病史。 [4]
Nephrotic Syndrome Diagnosed 確診腎病綜合徵
Past medical history was significant for the relapsing and remitting course of nephrotic syndrome diagnosed two years before presentation. [1] We present the case of a 51-year-old woman with nephrotic syndrome diagnosed 4 months previously. [2] MethodsChildren with nephrotic syndrome diagnosed between 1 and 18 years of age were followed prospectively from 1996 to 2016 at The Hospital for Sick Children (N = 377). [3] Methods Children with primary nephrotic syndrome diagnosed in Beijing Children's Hospital affiliated to Capital Medical University from January 2018 to March 2019 were enrolled. [4]既往病史對於就診前兩年診斷的腎病綜合徵的複發和緩解過程具有重要意義。 [1] 我們介紹了一個 4 個月前被診斷出患有腎病綜合徵的 51 歲女性病例。 [2] 方法 1996 年至 2016 年在兒童醫院 (N = 377) 對診斷為 1 至 18 歲的腎病綜合徵兒童進行前瞻性隨訪。 [3] 方法 入組2018年1月至2019年3月在首都醫科大學附屬北京兒童醫院確診的原發性腎病綜合徵患兒。 [4]
Ohvira Syndrome Diagnosed
OBJECTIVE This study aimed to analyze and compare patients with OHVIRA syndrome diagnosed in the prepubertal and postpubertal periods to understand the disease characteristics and improve clinical management. [1] We present 2 cases of OHVIRA syndrome diagnosed prepubertally. [2] We present 2 cases of OHVIRA syndrome diagnosed prepubertally. [3]客觀的 本研究旨在分析和比較青春期前和青春期後診斷的 OHVIRA 綜合徵患者，以了解疾病特徵並改善臨床管理。 [1] 我們介紹了 2 例青春期前診斷的 OHVIRA 綜合徵。 [2] 我們介紹了 2 例青春期前診斷的 OHVIRA 綜合徵。 [3]
Turner Syndrome Diagnosed
Objective: To report a case of Turner syndrome diagnosed in prenatal care. [1] 156 women with Turner Syndrome diagnosed from 1960-2014 using The Danish Cytogenetic Central Registry and linked them with the Danish National Patient Register and the Medication Statistics Register. [2]目的：報告一例在產前檢查中診斷為特納綜合徵的病例。 [1] 1960-2014 年使用丹麥細胞遺傳學中心登記處診斷出 156 名患有特納綜合徵的女性，並將她們與丹麥國家患者登記處和藥物統計登記處聯繫起來。 [2]
Good Syndrome Diagnosed
Thymoma may precede or present simultaneously with hypogammaglobulinemia and lymphopenia; however, cases of Good syndrome diagnosed years after thymectomy have been reported in literature as well [3, 4]. [1] Here, we describe a patient with Good Syndrome diagnosed with extensive candidal onychomycosis. [2]胸腺瘤可能先於或同時出現低丙種球蛋白血症和淋巴細胞減少症；然而，文獻也報導了在胸腺切除術後數年診斷出 Good 綜合徵的病例 [3, 4]。 [1] 在這裡，我們描述了一名被診斷為廣泛的念珠菌性甲真菌病的 Good Syndrome 患者。 [2]
Marfan Syndrome Diagnosed
In this study, we report the case of a patient with Marfan syndrome diagnosed at our centre at the age of 33 on the basis of typical clinical manifestations of this syndrome. [1] Early onset Marfan syndrome is the most severe form of Marfan syndrome diagnosed during perinatal period. [2]在這項研究中，我們根據該綜合徵的典型臨床表現，報告了一名 33 歲在我中心診斷的馬凡綜合徵患者的病例。 [1] 早發性馬凡綜合徵是圍產期診斷出的最嚴重的馬凡綜合徵。 [2]
Deletion Syndrome Diagnosed
2 deletion syndrome diagnosed between 1998 and 2019 at Pediatric Immunology Division of Ege University Faculty of Medicine and SBU Izmir Dr Behcet Uz Children's Education and Research Hospital were evaluated. [1] Case report: We report a case of 5p deletion syndrome diagnosed prenatally in association with mild ventriculomegaly, cerebellar hypoplasia, pontine hypoplasia, increased subarachnoid space and high suspicion of cortical hypoplasia with ultrasound, magnetic resonance imaging, and postmortem examination. [2]對 1998 年至 2019 年間在 Ege 大學醫學院兒科免疫學部和 SBU Izmir Behcet Uz 博士兒童教育和研究醫院診斷出的 2 缺失綜合徵進行了評估。 [1] 病例報告：我們報告一例產前診斷為 5p 缺失綜合徵的病例，伴有輕度腦室擴大、小腦發育不全、腦橋發育不全、蛛網膜下腔空間增加以及超聲、磁共振成像和死後檢查高度懷疑皮質發育不全。 [2]
Ovary Syndrome Diagnosed
Method A correlational study was carried out with 145 unmarried women with polycystic ovary syndrome diagnosed by a gynecologist using the Rotterdam Criteria of 2003 ( M age = 24. [1] Context: Polycystic ovary syndrome diagnosed by Rotterdam criteria, is the most common cause of anovulatory infertility. [2]方法採用2003年鹿特丹標準（Mage = 24. [1] 背景：鹿特丹標準診斷的多囊卵巢綜合徵是無排卵性不孕症的最常見原因。 [2]
Ligament Syndrome Diagnosed
We present a case of arcuate ligament syndrome diagnosed in a 23-year-old patient with epigastric pain, vomiting and weight loss, using Doppler ultrasound and CT-angiography, treated by surgical resection of the ligament with complete resolution of symptoms. [1] : We present a case of arcuate ligament syndrome diagnosed in a 23-year-old patient with epigastric pain, vomiting and weight loss, using Doppler ultrasound and CT-angiography, treated by surgical resection of the ligament with complete resolution of symptoms. [2]我們報告了一例弓狀韌帶綜合徵病例，患者為 23 歲患者，患者使用多普勒超聲和 CT 血管造影診斷為上腹痛、嘔吐和體重減輕，並通過手術切除韌帶進行治療，症狀完全消失。 [1] ：我們介紹了一例弓狀韌帶綜合徵病例，該病例診斷為一名 23 歲患者，患有上腹痛、嘔吐和體重減輕，使用多普勒超聲和 CT 血管造影，通過韌帶手術切除治療，症狀完全消退。 [2]
Overlap Syndrome Diagnosed 診斷出重疊綜合徵
Background: Sclerodermatomyosits is an overlap syndrome diagnosed when systemic sclerosis and dermatomyositis are observed in one patient, which develops simultaneously or sequentially. [1] We describe the first case of MG-LE overlap syndrome diagnosed after anti-PD1 immunotherapy for metastatic melanoma, which appeared after radiation therapy and then relapsed after brain radiation necrosis. [2]背景：硬皮肌炎是一種重疊綜合徵，當在一名患者中觀察到系統性硬化症和皮肌炎時診斷為同時或依次發展。 [1] 我們描述了第一例在轉移性黑色素瘤的抗 PD1 免疫治療後診斷出的 MG-LE 重疊綜合徵，該病例在放射治療後出現，然後在腦放射壞死後復發。 [2]
syndrome diagnosed according
Methods: Cross-sectional study where adult patients with irritable bowel syndrome diagnosed according to Rome IV criteria were included. [1] One trial of 39 participants recruited children with PFAPA syndrome diagnosed according to rigid, standard criteria. [2] The study included 60 patients with type I and type II diabetes with a depressive syndrome diagnosed according to the Beck and PHQ‑9 scales. [3] Methods: Patients with Sjögren’s Syndrome diagnosed according to the AECG classification criteria were included in this study. [4] Sixty women (18–30 years) with premenstrual syndrome diagnosed according to 30-item questionnaire were randomly assigned to receive either 30-mg zinc gluconate (group 1; n = 30) and/or placebo (group 2; n = 30) for 12 weeks. [5]方法：橫斷面研究納入了根據羅馬 IV 標準診斷的成人腸易激綜合徵患者。 [1] 一項包含 39 名參與者的試驗招募了根據嚴格的標準標準診斷為 PFAPA 綜合徵的兒童。 [2] 該研究包括 60 名 I 型和 II 型糖尿病患者，根據 Beck 和 PHQ-9 量表診斷為抑鬱綜合徵。 [3] 方法：本研究納入根據 AECG 分類標準診斷的干燥綜合徵患者。 [4] 根據 30 項問卷調查診斷為經前期綜合徵的 60 名女性（18-30 歲）被隨機分配接受 30 毫克葡萄糖酸鋅（第 1 組；n = 30）和/或安慰劑（第 2 組；n = 30）治療。 12 週。 [5]
syndrome diagnosed prenatally 產前診斷的綜合徵
This child had complete atrioventricular septal defect associated with mild left ventricular hypoplasia and Down syndrome diagnosed prenatally. [1] In one of them, the phenotypic syndrome diagnosed prenatally was different from that diagnosed in the postnatal period. [2] Case report: We report a case of 5p deletion syndrome diagnosed prenatally in association with mild ventriculomegaly, cerebellar hypoplasia, pontine hypoplasia, increased subarachnoid space and high suspicion of cortical hypoplasia with ultrasound, magnetic resonance imaging, and postmortem examination. [3] Very few cases of Pai syndrome diagnosed prenatally have been described. [4]這個孩子有與輕度左心室發育不全和產前診斷的唐氏綜合徵相關的完全房室間隔缺損。 [1] 其中之一，產前診斷的表型綜合徵與產後診斷的表型綜合徵不同。 [2] 病例報告：我們報告一例產前診斷為 5p 缺失綜合徵的病例，伴有輕度腦室擴大、小腦發育不全、腦橋發育不全、蛛網膜下腔空間增加以及超聲、磁共振成像和死後檢查高度懷疑皮質發育不全。 [3] 很少有產前診斷的 Pai 綜合徵病例被描述。 [4]
syndrome diagnosed prepubertally
We present 2 cases of OHVIRA syndrome diagnosed prepubertally. [1] We present 2 cases of OHVIRA syndrome diagnosed prepubertally. [2]我們介紹了 2 例青春期前診斷的 OHVIRA 綜合徵。 [1] 我們介紹了 2 例青春期前診斷的 OHVIRA 綜合徵。 [2]