
Gliomas - Symptoms, diagnosis and treatment | BMJ Best Practice
2025年1月15日 · IDH-wildtype diffuse glioma (glioblastoma) is an aggressive primary brain tumour that presents in patients in the sixth or seventh decade of life. IDH-mutant gliomas (including oligodendroglioma, IDH-mutant, 1p/19q codeleted, grades 2-3; and astrocytoma, IDH-mutant, grades 2-4) tend to occur in young or middle-age patients.
Gliomas - Sintomas, diagnóstico e tratamento | BMJ Best Practice
2025年2月28日 · O glioma difuso de tipo selvagem da IDH (glioblastoma) é um tumor cerebral primário agressivo que se apresenta em pacientes na sexta ou sétima décadas de vida. Gliomas com mutações em IDH (tais como oligodendroglioma, com mutação em IDH e codeleção de 1p/19q, graus 2-3; e astrocitoma, com mutação em IDH, graus 2-4) tendem a ocorrer ...
Long QT syndrome - Symptoms, diagnosis and treatment - BMJ …
2023年8月29日 · Long QT syndrome (LQTS) is a congenital or acquired condition that is characterised by a prolonged QT interval on the surface ECG and is associated with a high risk of sudden cardiac death due to ventricular tachyarrhythmias.
Neurofibromatose do tipo 1 - BMJ Best Practice
2025年2月28日 · A neurofibromatose do tipo 1 (NF1) é um distúrbio genético autossômico dominante definida pelas características de manchas café-com-leite, múltiplos neurofibromas e nódulos de Lisch na íris.
Symptoms, diagnosis and treatment - BMJ Best Practice
2024年5月3日 · Tumour lysis syndrome (TLS) is an oncological emergency caused by rapid breakdown of cancer cells and subsequent release of large amounts of intracellular content into the bloodstream.
Faecal incontinence in children - BMJ Best Practice
2022年8月9日 · Faecal incontinence in children is the involuntary passage of stool from the rectum through the anus resulting in episodes of stooling at inappropriate times, occurring at an age after which toilet training is typically complete (in most, 4 years of age or older).
Symptoms, diagnosis and treatment - BMJ Best Practice US
2023年6月29日 · Meningiomas are the most common primary tumor of the cranial and spinal compartments. Estimates indicate that they represent 39.7% of all primary central nervous system tumors, and 55.4% of all nonmalignant tumors.
Symptoms, diagnosis and treatment - BMJ Best Practice
2022年6月7日 · Type 1 neurofibromatosis (NF1) is an autosomal-dominant genetic disorder with the defining features of café au lait spots, multiple neurofibromas, and iris Lisch nodules.
Symptoms, diagnosis and treatment - BMJ Best Practice
2023年11月21日 · Tuberous sclerosis complex is an autosomal-dominant, neurocutaneous, multi-system disorder characterised by cellular hyperplasia, tissue dysplasia, and multiple organ hamartomas.
Differential diagnosis of symptoms - BMJ Best Practice
2025年3月4日 · Introduction. Delirium is an acute, fluctuating change in mental status, with inattention, disorganized thinking, and altered levels of consciousness.