Short stature due to endocrine disorder
ICD-10 E34.3 is a billable code used to indicate a diagnosis of short stature due to endocrine disorder.
Short stature due to endocrine disorders encompasses a variety of conditions that impede normal growth and development in children and adolescents. This can include disorders related to the pituitary gland, such as growth hormone deficiency, which is critical for normal growth. Additionally, conditions affecting the thyroid gland, such as hypothyroidism, can lead to reduced growth rates. Disorders of puberty, including delayed puberty or hypogonadism, can also contribute to short stature by delaying the onset of growth spurts. Polyglandular dysfunction syndromes, where multiple endocrine glands are affected, can further complicate the clinical picture. Thymus disorders, while primarily associated with immune function, can also indirectly affect growth through their influence on overall health and metabolic processes. Growth abnormalities may manifest as a result of these endocrine disorders, necessitating a comprehensive evaluation to determine the underlying cause and appropriate management strategies.
Growth charts, hormonal assay results, and detailed patient history.
Evaluation of a child presenting with short stature and delayed puberty.
Consideration of familial short stature versus pathological causes.
Comprehensive endocrine evaluations, including imaging studies and lab results.
Management of a patient with growth hormone deficiency and associated short stature.
Need for interdisciplinary collaboration with pediatricians for holistic care.
Used to evaluate suspected growth hormone deficiency in a child with short stature.
Document the reason for testing and any previous growth measurements.
Endocrinologists may require additional tests to confirm diagnosis.
Common causes include growth hormone deficiency, hypothyroidism, and disorders affecting puberty such as hypogonadism. Polyglandular dysfunction syndromes can also contribute to short stature.
