Thyroid disease
Thyroid disease
A public condition summary is being prepared.
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Browse public condition summaries from China medical resources by stable specialty category.
Thyroid disease
A public condition summary is being prepared.
View detailsOsteochondrosis
Osteochondrosis is a non-inflammatory condition affecting articular cartilage and epiphyseal cartilage. Common sites of involvement include the femoral head, tibial tuberosity, tarsal navicular bone, carpal lunate bone, and calcaneal apophysis. It primarily affects adolescents, presenting mainly with joint swelling and pain.
View detailsExtrapyramidal diseases
Extrapyramidal diseases, also known as movement disorders, refer to impaired regulation of body movements during voluntary actions. They primarily manifest in two ways: one is hypokinesia due to increased muscle tone, characterized by poverty of movement (e.g., Parkinson's disease); the other is hyperkinesia due to decreased muscle tone (e.g., chorea). Symptoms vary among patients with different etiologies. For conditions primarily characterized by hypokinesia, the most common symptoms are limb tremor, limb rigidity, and abnormal gait. For conditions primarily characterized by hyperkinesia, the most common symptoms are dance-like involuntary movements and decreased muscle tone.
Congenital adrenal hyperplasia
Congenital adrenal hyperplasia (CAH) is a relatively common autosomal recessive genetic disorder caused by congenital defects in enzymes required for corticosteroid synthesis. Due to the defect in corticosteroid synthesis, the body's endocrine regulatory center secretes excessive adrenocorticotropic hormone (ACTH) to increase the levels of these hormones. This leads to adrenal cortical hyperplasia and the secretion of excessive cortisol precursors, such as 11-deoxycortisol and adrenal androgens, resulting in a series of clinical symptoms. This disease is a class of disorders, including 21-hydroxylase deficiency, 11β-hydroxylase deficiency, 17-hydroxylase deficiency, 3β-hydroxysteroid dehydrogenase deficiency, corticosterone methyl oxidase deficiency, and congenital lipoid adrenal hyperplasia.
View detailsTracheal stenosis
Tracheal stenosis is a disease characterized by dyspnea caused by tracheal cartilage framework deformity, collapse, or defect, tracheal mucosal scar formation, or submucosal tissue hyperplasia due to various reasons. Common manifestations of this disease include dyspnea, cough, hemoptysis, and stridor.
View detailsAtrial septal defect
Atrial septal defect (ASD) refers to a condition where a portion of the septum between the right and left atria of the heart fails to close completely during fetal development. ASD accounts for approximately 10% of all congenital heart diseases, ranking as the second most common congenital heart disease in children. It accounts for 20% to 30% of congenital heart diseases in adults, making it the most common congenital heart disease in adults. It is more prevalent in females than males. Common Questions Q: Does atrial septal defect affect pregnancy? A: The impact of atrial septal defect on pregnancy varies depending on the specific condition of the pregnant woman. Although cardiac load increases during pregnancy, young pregnant women with simple defects can tolerate pregnancy, even multiple pregnancies, without significant adverse outcomes. However, if there is a history of certain arrhythmias or heart failure, the risk of pregnancy increases, requiring close monitoring. There is a higher risk of specific venous embolisms and abnormal blood shunting during delivery compared to the general population. If there is coexisting significant pulmonary vascular disease, the risk of maternal and fetal mortality is high, and pregnancy should be avoided in such cases.
View detailsVentricular septal defect
The septum between the left and right ventricles of the heart is called the ventricular septum. An intact ventricular septum prevents blood flow between the left and right ventricles. Ventricular septal defect (VSD) is a condition where there is a hole in the ventricular septum, causing blood from the left and right ventricles to mix, leading to a series of problems. It is the most common congenital heart disease. The symptoms of VSD vary. If the defect is small, there are usually no obvious symptoms. If the defect is large, it can manifest as shortness of breath and fatigue after activity, and in severe cases, it can lead to growth and developmental delays.
View detailsMeningitis
Meningitis is a group of acute inflammatory diseases of the meninges caused by various infections. The two more common types are: Viral meningitis Bacterial meningitis: This includes purulent meningitis, tuberculous meningitis, and cryptococcal meningitis. This disease is more common in infants and children. Key symptoms include fever, headache, nausea, vomiting, and neck stiffness.
View detailsHyperprolactinemia
Hyperprolactinemia is a condition characterized by abnormally elevated serum prolactin levels due to various causes. It can affect both men and women, though it is more common in women. Typical clinical symptoms of hyperprolactinemia in women include menstrual irregularities, galactorrhea, infertility, and sexual dysfunction. In men, typical clinical symptoms include sexual dysfunction, decreased secondary sexual characteristics, and oligozoospermia or infertility.
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