Some people with Albright syndrome can be seen as early as 4 months after birth, most are not visible until 11-30 years of age. Albright syndrome is characterized by fibrous developmental abnormalities of the bone, limited hyperpigmented spots, and precocious puberty. The etiology is unknown and it is a congenital anomaly. According to the Chinese Clinical Dermatology, the disease can develop as early as 4 months to 2 years after birth, and there are statistics that 69% of the 11-30 year olds develop the disease, with females slightly more than males. Bone damage often involves the long bones of the limbs, pelvis, skull, etc., manifesting as diffuse fibrous osteitis, which may be accompanied by pain or asymptomatic. Pigmented spots occur in the back, buttocks, thighs and other parts of the brown or light brown spots, irregular edges, distribution is not symmetrical. Some patients under the age of 10 have symptoms of precocious puberty, such as enlarged breasts, menstruation, and premature growth of pubic hair and armpit hair. Patients should consult a doctor for appropriate examination to avoid delaying their condition when they develop precocious puberty, abnormal pigmentation, and growth abnormalities such as short stature.