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Neonatal hemolytic disease due to anti-Diego(a) antibody: a case report

期刊: JOURNAL OF MEDICAL CASE REPORTS, 2022; 16 (1)

Background The Diego(a) antigen commonly occurs in certain Asian and South American Indian populations. In general, hemolysis caused by anti-Diego(a) ......

A novel apolipoprotein E mutation, ApoE Ganzhou (Arg43Cys), in a Chinese son and his father with lipoprotein glomerulopathy: two case reports

期刊: JOURNAL OF MEDICAL CASE REPORTS, 2022; 16 (1)

Background Lipoprotein glomerulopathy is a rare and newly recognized glomerular disease that can lead to kidney failure. Its pathological features inc......

Successful treatment of an infant with congenital bile acid synthesis disorder type 3 by ursodeoxycholic acid: a case report

期刊: JOURNAL OF MEDICAL CASE REPORTS, 2022; 16 (1)

Background: Congenital bile acid synthesis disorder type 3 caused by oxysterol 7 alpha-hydroxylase deficiency is an extremely rare genetic liver disea......

Systemic lupus erythematosus with trisomy X: a case report and review of the literature

期刊: JOURNAL OF MEDICAL CASE REPORTS, 2022; 16 (1)

Background The cause of systemic lupus erythematosus is not completely clear so far, but the prevalence of systemic lupus erythematosus is significant......

Electroacupuncture as an effective therapy for Tapia's syndrome after transoral intubation for general anesthesia: a case report and review of the literature

期刊: JOURNAL OF MEDICAL CASE REPORTS, 2022; 16 (1)

Background Tapia's syndrome is a rare complication of airway manipulation under general anesthesia. Injuries to the vagus nerve (X) and hypoglossal ne......

Microvascular decompression for trigeminal neuralgia caused by persistent trigeminal artery associated with craniosynostosis: a case report

期刊: JOURNAL OF MEDICAL CASE REPORTS, 2022; 16 (1)

Background Persistent trigeminal artery (PTA) is a rare arterial anastomosis between the basilar artery (BA) and internal carotid artery (ICA). It pla......

High-dose intravenous glucocorticoid induces hyperamylasemia: a case series

期刊: JOURNAL OF MEDICAL CASE REPORTS, 2022; 16 (1)

Background Glucocorticoids have many side effects, and high-dose intravenous application may cause rare adverse reactions such as hyperamylasemia. The......

Cerebrovascular intervention therapy worked positively in one patient with severe cerebral venous sinus thrombosis due to hyperthyroidism: a case report and review of the literature

期刊: JOURNAL OF MEDICAL CASE REPORTS, 2022; 16 (1)

Background With further understanding of cerebral venous sinus thrombosis, hyperthyroidism has gradually been revealed as a rare predisposing factor f......

Acute coronary syndrome in an 8-year-old child with familial hypercholesterolemia: a case report

期刊: JOURNAL OF MEDICAL CASE REPORTS, 2022; 16 (1)

Background Familial hypercholesterolemia (FH) is the most commonly inherited metabolic disease and has an autosomal dominant mode of inheritance. Pati......

Chronic inflammatory demyelinating polyneuropathy with anti-contactin-associated protein 1 antibody and bile duct hamartomas in the liver: a case report

期刊: JOURNAL OF MEDICAL CASE REPORTS, 2022; 16 (1)

Background Autoantibodies targeting node of Ranvier proteins are rarely reported in China. Case presentation We present the case of a 66-year-old Chin......

Epidermal nevus syndrome with the mutation of PTCH1 gene and cerebral infarction: a case report and review of the literature

期刊: JOURNAL OF MEDICAL CASE REPORTS, 2022; 16 (1)

Background Epidermal nevus syndrome is a group of congenital neuroectodermal and/or mesodermal disorders characterized by the epidermal nevi in common......

Capecitabine-induced severe diabetes and hypokalemia: a case report

期刊: JOURNAL OF MEDICAL CASE REPORTS, 2022; 16 (1)

Background Capecitabine is widely used in chemotherapy for breast, colorectal, and gastric cancers. The frequent adverse reactions of capecitabine mai......

Waardenburg syndrome type 4 coexisting with open-angle glaucoma: a case report

期刊: JOURNAL OF MEDICAL CASE REPORTS, 2022; 16 (1)

Background Waardenburg syndrome is an autosomal dominant disorder with varying degrees of sensorineural hearing loss as well as abnormal pigmentation ......

A novel missense mutation in complement factor I predisposes patients to atypical hemolytic uremic syndrome: a case report

期刊: JOURNAL OF MEDICAL CASE REPORTS, 2022; 16 (1)

Background Atypical hemolytic uremic syndrome, also called the nondiarrheal form of hemolytic uremic syndrome, is a rare disease characterized by the ......

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