Hecht Scott syndrome
Hecht Scott syndrome is a rare genetic disorder characterized by delayed development, intellectual disability, distinctive facial features, and skeletal abnormalities.
Symptoms[edit | edit source]
The symptoms of Hecht Scott syndrome include:
Causes[edit | edit source]
Hecht Scott syndrome is caused by mutations in the genes that are involved in the development of the brain and the skeletal system.
Diagnosis[edit | edit source]
The diagnosis of Hecht Scott syndrome is based on the clinical symptoms and confirmed by genetic testing.
Treatment[edit | edit source]
The treatment of Hecht Scott syndrome is symptomatic and supportive. This may include physical therapy, occupational therapy, and speech therapy.
Prognosis[edit | edit source]
The prognosis of Hecht Scott syndrome varies depending on the severity of the symptoms. Some individuals with this syndrome may have a normal lifespan, while others may have a shortened lifespan due to complications from the disorder.
See also[edit | edit source]
Hecht Scott syndrome Resources | ||
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Contributors: Prab R. Tumpati, MD