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A.M.A. American journal of diseases of children最新文献

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Hashimoto's disease in childhood. 儿童桥本氏病。
Pub Date : 1955-08-01 DOI: 10.1001/archpedi.1955.04030010175007
H C DAVIS, E A HANSKE
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引用次数: 8
Strychnine poisoning; case report of fatality in a fifteen-month-old child. 马钱子碱中毒;报告一名15个月大的婴儿死亡。
H C LEIFHEIT, W KNOPP
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引用次数: 0
Pseudohypoparathyroidism; report of a case in a sixteen-month-old girl. Pseudohypoparathyroidism;报告一例16个月大的女婴。
B B OBERST, C A TOMPKINS
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引用次数: 0
The developmental evaluation of the blind premature infant. 失明早产儿的发育评价。
Pub Date : 1955-08-01 DOI: 10.1001/archpedi.1955.04030010137002
A H PARMELEE
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引用次数: 10
Ulcerative colitis in children; observations in selected patients. 儿童溃疡性结肠炎;对选定患者的观察。
J B KIRSNER, H F RASKIN, W L PALMER
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引用次数: 0
Pseudohypoparathyroidism; report of a case in a sixteen-month-old girl. Pseudohypoparathyroidism;报告一例16个月大的女婴。
Pub Date : 1955-08-01 DOI: 10.1001/ARCHPEDI.1955.04030010207014
B. Oberst, C. Tompkins
INTRODUCTION IN THE year 1942, Albright, Burnett, Smith, and Parson1first reported three cases of pseudohypoparathyroidism which they termed Seabright Bantam syndrome because of the end-organ apparently being refractory to endocrine stimulation. This is a relatively rare condition. There are about 16 cases reported in the literature.* This report is Case 17 and is the youngest on record. The syndrome is characterized by (1) hypocalcemia, (2) hyperphosphatemia, (3) manifestations of tetany, and (4) calcium deposits in the basal ganglia and subcutaneous tissue.14In this condition, biopsy shows normal parathyroid tissue and the patients fail to respond to parathyroid extract. Clinically, the patient demonstrates a moon-shaped face, strabismus, short neck, brachydactylia due to early fusion of the metacarpals, obesity, and short stature. Respiratory symptoms, tetany, or other central nervous system manifestations may be present. Mental retardation is a common problem. The differential diagnosis must include Mongolism and cretinism. REPORT
1942年,Albright、Burnett、Smith和parson1首次报道了3例假性甲状旁腺功能减退症,他们称其为Seabright Bantam综合征,因为终末器官对内分泌刺激明显不耐受。这是一种相对罕见的情况。文献中报道了大约16例。*本报告是第17例,是有记录以来最年轻的病例。该综合征的特点是:(1)低钙血症,(2)高磷血症,(3)抽搐的表现,(4)基底神经节和皮下组织的钙沉积。在这种情况下,活检显示甲状旁腺组织正常,患者对甲状旁腺提取物没有反应。临床表现为月型脸、斜视、短颈、掌骨早期融合导致的短指、肥胖和身材矮小。可能出现呼吸系统症状、手足搐搦或其他中枢神经系统表现。智力迟钝是一个普遍的问题。鉴别诊断必须包括蒙古病和克汀病。报告
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引用次数: 3
Cutaneous Cuterebra myiasis; an unusual case in an infant. 皮肤锥体丝虫病;一个罕见的婴儿病例。
F J HODGES
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引用次数: 0
Ulcerative colitis in children; observations in selected patients. 儿童溃疡性结肠炎;对选定患者的观察。
Pub Date : 1955-08-01 DOI: 10.1001/ARCHPEDI.1955.04030010143003
J. Kirsner, H. Raskin, W. Palmer
INTRODUCTION Ulcerative colitis is not rare in children. Bargen and Kennedy1recently reviewed 139 patients observed during a period of 10 years. Smaller groups of cases have been described by others* During the 18 years 1936 to 1954, eighty instances of ulcerative colitis in children have been observed at the University of Chicago. The purpose of this report is to describe four selected patients, illustrating important diagnostic and therapeutic aspects of this complex illness. Case1.—N. M., a 14-year-old white girl student, first experienced mild diarrhea while vacationing in Florida in January, 1953. On returning to Chicago, her bowel movements became numerous and bloody. Although Endamoeba histolytica never was identified, she was treated elsewhere with emetine and later oxytetracycline (Terramycin). After initial improvement, the symptoms recurred, but responded to bed rest and a bland diet. Roentgen examination elsewhere, in November, 1953, indicated minimal changes in the right colon and
溃疡性结肠炎在儿童中并不罕见。Bargen和kennedy1最近回顾了10年间观察到的139例患者。在1936年至1954年的18年间,芝加哥大学观察到80例儿童溃疡性结肠炎。本报告的目的是描述四个选定的病人,说明重要的诊断和治疗方面的这种复杂的疾病。Case1.-N。1953年1月,14岁的白人女学生M在佛罗里达度假时首次出现轻度腹泻。回到芝加哥后,她的大便变得频繁而血腥。虽然从未发现溶组织内阿米巴原虫,但她在其他地方接受了依美丁和后来的土霉素土霉素治疗。在最初的改善后,症状复发,但对卧床休息和温和饮食有反应。1953年11月,其他地方的伦琴检查显示右结肠和
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引用次数: 10
Congenital mitral atresia with hypoplastic nonfunctioning left heart. 先天性二尖瓣闭锁伴左心发育不全。
Pub Date : 1955-08-01 DOI: 10.1001/archpedi.1955.04030010178009
S FRIEDMAN, L MURPHY, R ASH
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引用次数: 24
Strychnine poisoning; case report of fatality in a fifteen-month-old child. 马钱子碱中毒;报告一名15个月大的婴儿死亡。
Pub Date : 1955-08-01 DOI: 10.1001/ARCHPEDI.1955.04030010201012
H. Leifheit, W. Knopp
THE ROLE of strychnine in homicide and suicide is well established in the annals of legal medicine and toxicology. Occasionally strychnine is featured as the agent in accidental poisonings, the most tragic being those cases involving fatalities in children due to their ingestion of some candy-coated proprietary drug or medicine containing the poison. This communication is an account of such a case. REPORT OF CASE A 15-month-old white boy had been playing in his parents' bedroom. The parents noticed that the infant looked ill, and he cried out as if in pain. These symptoms were followed by jerking movements and appearance of a blue coloration of the skin. The baby was rushed to the nearest medical facility, and while en route it was necessary for the father to administer artificial respiration on two separate occasions. As the child had been seen playing with "camphor balls," a history of suspected poisoning
士的宁在杀人和自杀中的作用在法律医学和毒理学的编年史上得到了很好的证实。士的宁偶尔也会在意外中毒中起作用,最悲惨的是那些儿童因摄入含有这种毒药的糖衣专有药物或药物而死亡的案件。本通讯就是对这种情况的叙述。一个15个月大的白人男孩一直在他父母的卧室里玩耍。父母注意到婴儿看起来病了,他哭了起来,好像很痛苦。这些症状之后是抽搐运动和皮肤出现蓝色。婴儿被紧急送往最近的医疗机构,在途中,父亲有必要两次进行人工呼吸。由于这名儿童曾被目击玩“樟脑球”,有疑似中毒史
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引用次数: 0
期刊
A.M.A. American journal of diseases of children
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