Decreased β-cell function in a case with Becker muscular dystrophy accompanied by post-transplant diabetes [0.03%]
贝克尔型肌营养不良症伴发移植后糖尿病一例及对β细胞功能的探讨
Kazuya Motohashi,Takaaki Murakami,Daisuke Otani et al.
Kazuya Motohashi et al.
Summary: Duchenne and Becker muscular dystrophy (DMD/BMD) are genetic disorders characterized by progressive muscle degeneration due to alterations of the dystrophin protein. The degeneration of skeletal muscles and subse...
Mauriac syndrome: a rare complication in patients with type 1 diabetes mellitus [0.03%]
1型糖尿病患者中毛里亚克综合征的罕见并发症报告
João Oliveira Torres,Diana Cruz Martins,Alexandra Abegão Matias et al.
João Oliveira Torres et al.
Summary: Mauriac syndrome is a rare complication in patients with type 1 diabetes. It presents with poor glycemic control and hepatomegaly due to extensive liver glycogen deposition. Whether behavioral or genetic factors ...
SGLT2 inhibitor administration to two patients with diabetes mellitus with ascites due to cirrhosis [0.03%]
两名由肝硬化导致腹水的糖尿病患者使用钠-葡萄糖协同转运蛋白2抑制剂治疗病例报告
Koji Nagayama,Risako Harada,Hiroshi Ajima et al.
Koji Nagayama et al.
Summary: We used the sodium-glucose cotransporter 2 inhibitor, luseogliflozin in two patients with diabetes mellitus with Child-Pugh classification B cirrhosis and cirrhotic ascites. In each case, luseogliflozin was safel...
'Un-thirsty' hypernatremia [0.03%]
'不解渴'的高钠血症
Markus Koster,Katrin Ledergerber,Michael Brändle
Markus Koster
Summary: A 38-year-old man was admitted because of transient somnolence. Five weeks previously, he had suffered a subarachnoid hemorrhage from a ruptured aneurysm of the anterior communicating artery (ACOM), which was tre...
Delayed diagnosis of STAT1 gain-of-function variant in a patient with multiple endocrine autoimmunity and recurrent fungal infections [0.03%]
STAT1基因功能获得性变异型所致自身免疫多内分泌病和复发性真菌感染的延迟诊断
Sydney Sparanese,Rae Brager,David Fahmy et al.
Sydney Sparanese et al.
Summary: This case report describes a 54-year-old woman with multiple endocrine autoimmune pathologies and recurrent mucocutaneous Candida spp. infections that were inappropriately attributed to her glycemic control. Foll...
Severe hypertriglyceridaemia with length-related small fibre sensory neuropathy as a complication of previous gestational diabetes mellitus [0.03%]
既往妊娠糖尿病的并发症严重高甘油三酯血症伴长度相关的小纤维感觉神经病
Fatima Iqbal,Daniel Lim,Ruby Chang et al.
Fatima Iqbal et al.
Summary: Gestational diabetes mellitus (GDM) is a known risk factor for dyslipidaemias. Insulin resistance and the associated dyslipidaemia, particularly hypertriglyceridaemia, have been less frequently linked to peripher...
A case of hypopituitarism with pancytopenia cured by corticosteroid and thyroid hormone replacement therapy [0.03%]
糖皮质激素及甲状腺激素替代治疗一例全血细胞减少的垂体功能减退症患者治愈报告
Violeta Mladenovic,Radica Zivkovic Zaric,Snezana Sretenovic et al.
Violeta Mladenovic et al.
Summary: Pancytopenia associated with hypopituitarism has been reported in the literature as a rare occurrence limited to isolated case reports, predominantly associated with Sheehan syndrome. We present the case of a 31-...
High-risk pregnancy complicated by craniopharyngioma: diagnosis in the context of visual impairment and tumor resection during pregnancy following IVF [0.03%]
辅助生育后妊娠合并颅咽管瘤一例：视力减退发现诊断和孕期肿瘤切除的挑战性病例
Yuki Tsujimoto,Kenji Yamashiro,Yui Watanabe et al.
Yuki Tsujimoto et al.
Summary: This report describes the case of a 37-year-old woman diagnosed with a craniopharyngioma during pregnancy. The patient initially presented with visual impairment at 15 weeks of gestation, and MRI revealed a cysti...
Maxim John Levy Barnett,Sarah Eidbo,Ana Rivadeneira
Maxim John Levy Barnett
Summary: Levothyroxine is the backbone of hypothyroidism treatment. The dosage of levothyroxine varies; however, as an estimate, an average adult patient will require 1.6 micrograms per kilogram of body weight. We present...
Identification of an ABCC8 variant in a kindred with transient diazoxide responsive hyperinsulinism [0.03%]
在可卡因唑酯治疗反应型一过性高胰岛素血症家系中鉴定ABCC8变异型
Ryan L Smith,Stephen I Stone
Ryan L Smith
Summary: Congenital hyperinsulinism is a rare disorder characterized by hypoglycemia and inappropriately elevated insulin levels. The genetics of congenital hyperinsulinism is complex, with the most common cause being pat...