Somatotropin deficiency

From WikiMD's Food, Medicine & Wellness Encyclopedia

Somatotropin Deficiency is a medical condition characterized by the inadequate production of somatotropin, also known as growth hormone (GH), by the pituitary gland. This condition can occur at any age and can lead to a variety of health issues, including short stature in children and metabolic abnormalities in adults.

Causes[edit | edit source]

Somatotropin deficiency can be caused by a variety of factors. These include genetic mutations, damage to the pituitary gland due to surgery or radiation, certain types of tumors, and certain medical conditions such as Turner syndrome and Prader-Willi syndrome. In many cases, the cause of the deficiency is unknown, a condition referred to as idiopathic somatotropin deficiency.

Symptoms[edit | edit source]

The symptoms of somatotropin deficiency vary depending on the age at which the deficiency occurs. In children, the most common symptom is a slower than normal growth rate, leading to short stature. Other symptoms can include delayed puberty, increased fat around the waist and face, and a younger appearance than peers.

In adults, symptoms can include changes in body composition such as increased fat and decreased muscle mass, fatigue, reduced exercise tolerance, and decreased bone density, which can lead to osteoporosis.

Diagnosis[edit | edit source]

Diagnosis of somatotropin deficiency involves a series of tests, including blood tests to measure levels of IGF-1, a hormone that is regulated by somatotropin. Other tests may include stimulation tests, where a substance is given to stimulate the pituitary gland to release somatotropin, and imaging tests such as MRI to identify any abnormalities in the pituitary gland.

Treatment[edit | edit source]

Treatment for somatotropin deficiency typically involves replacement therapy with synthetic somatotropin. This treatment can help to increase growth in children and improve body composition, energy levels, and bone density in adults. Treatment is usually lifelong and requires regular monitoring to ensure effectiveness and adjust dosage as necessary.

See Also[edit | edit source]

Template:Endocrine, nutritional and metabolic disease


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Contributors: Prab R. Tumpati, MD