Precocious Puberty

What is precocious puberty?

precocious puberty is the onset of secondary sexual characteristics before a normal age. Although it is difficult to define normal age ranges because of the marked variation with which puberty begins in normal children, precocious puberty can be defined as the onset of puberty before the age of 8 years in girls or 9 years in boys.

Symptoms may affect multiple parts of the body. Understanding which part of the body a symptom affects can help us to better understand the potential underlying causes of a symptom, including a rare disease or genetic syndrome.

Symptoms may affect multiple parts of the body. Understanding which part of the body a symptom affects can help us to better understand the potential underlying causes of a symptom, including a rare disease or genetic syndrome.

Developmental symptoms may affect different parts of an individual’s development. These include their emotional and social development, their physical development, as well as their cognitive and communication skills.

Developmental milestones help to track a child’s developmental progress and flag a delay. A delay may be isolated or accompanied by other developmental delays either in the same area and/or in other areas too.

Symptoms relating to development may be many and wide-ranging. They can include a walking delay, issues with speech and language including late talking, trouble socializing with others or with showing emotion.

What should I do next?

In some instances, precocious puberty may be one of the features of a rare disease or genetic syndrome. To find out if someone with precocious puberty, may be due to a genetic syndrome, it is important to have a consultation and evaluation with a clinical genetic specialist. Specialists may also suggest specific genetic testing or other types of tests to help reach a diagnosis. FDNA’s AI technology can help speed up the diagnostic process by analyzing facial features and other health information.

More signs and symptoms

Signs & Symptoms

Hyperkinetic Movements

Hyperkinetic movements are repetitive, abnormal and involuntary movements of the body. These motions are identified as common neural disturbances in children and can potentially lead to movement disorders. The distribution and severity of these repeated movements may shift over time.

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Signs & Symptoms

Rieger Anomaly

Reiger anomaly is an ocular defect characterized by serious deformity in the anterior chamber of the eye with noticeable strands and shrinking of the iris stroma. This congenital malformation of the anterior segment is identified by iridocorneal malformation, glaucoma, iris stromal hypoplasia, posterior embryotoxon, and corneal opacities.

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Signs & Symptoms

Restrictive Behavior

Restrictive behavior is a form of behavior characterized by an abnormal limitation to a few interests and activities. Children may engage in repetitive motor movements or speech and may continually employ the same routine.

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