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Progeria
Progeria, also known as Hutchinson-Gilford syndrome, may be autosomal recessive. Male patients are more common than female patients. They grow and develop normally within one year old, and then gradually develop premature aging changes. It is a rare disease characterized by metabolic abnormalities, developmental disorders and dwarfism, accompanied by incomplete development of bones, teeth, nails, hair and fat, and the appearance of an old man and arteriosclerosis in childhood. Most children have normal intelligence, but their blood lipids are increased and the production of growth hormone is reduced by 50% compared to normal.
  • Site of disease:

    Craniocerebral and whole body
  • Infectious :

    Not contagious
  • Frequent population:

    child
  • Related symptoms:

    Joint stiffness Cyanosis around the mouth and nose Congenital premature graying of hair Disappearance of subcutaneous fat Stomach ache
  • Concurrent disease:

Related Drugs
aspirin
Indication: 1. Analgesic and antipyretic; 2. Anti-inflammatory and anti-rheumatic; 3. Arthritis; 4. Anti-thrombotic; 5. Mucocutaneous lymph node syndrome (Kawasaki disease); 6. Prevention of gastrointestinal tumors; 7. Inhibition of platelet aggregation.
aspirin
Indication: 1. Analgesic and antipyretic; 2. Anti-inflammatory and anti-rheumatic; 3. Arthritis; 4. Anti-thrombotic; 5. Mucocutaneous lymph node syndrome (Kawasaki disease); 6. Prevention of gastrointestinal tumors; 7. Inhibition of platelet aggregation.
Manufacturer:

Wuyi Cihang Pharmaceutical Co., Ltd.

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