Stratton Parker syndrome

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Stratton-Parker Syndrome

Stratton-Parker Syndrome (pronounced: stra-ton par-ker sin-drome) is a rare genetic disorder characterized by a variety of symptoms including intellectual disability, microcephaly, and seizures. The syndrome is named after the researchers who first described it, Dr. Stratton and Dr. Parker.

Etymology

The term "Stratton-Parker Syndrome" is derived from the names of the two researchers who first described the syndrome, Dr. Stratton and Dr. Parker. The term "syndrome" comes from the Greek word "syndromē", which means "concurrence of symptoms" or "running together".

Symptoms

Stratton-Parker Syndrome is characterized by a variety of symptoms, which can vary greatly in severity. These include:

  • Intellectual disability: This is a common symptom of Stratton-Parker Syndrome. Individuals with this condition often have difficulties with learning and understanding new information.
  • Microcephaly: This is a condition where the head is significantly smaller than normal. It is often present at birth in individuals with Stratton-Parker Syndrome.
  • Seizures: Many individuals with Stratton-Parker Syndrome experience seizures. These can range from mild to severe and can be difficult to control with medication.

Diagnosis

Diagnosis of Stratton-Parker Syndrome is based on the presence of characteristic symptoms and a detailed patient history. Genetic testing may also be used to confirm the diagnosis.

Treatment

Treatment for Stratton-Parker Syndrome is symptomatic and supportive. This may include medications to control seizures, special education programs for intellectual disability, and various therapies to help manage other symptoms.

Prognosis

The prognosis for individuals with Stratton-Parker Syndrome varies greatly depending on the severity of symptoms. With appropriate treatment and support, many individuals with this condition can lead fulfilling lives.

See Also

External links

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