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Pediatric Endocrine Disorders

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Turner Syndrome

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A chromosomal disorder in females where one X chromosome is completely or partially missing.

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Type 2 Diabetes Mellitus

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A metabolic disorder characterized by insulin resistance, resulting in high blood glucose levels.

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Growth Hormone Deficiency

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A lack of growth hormone resulting in short stature and slow growth rates.

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Precocious Puberty

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The early onset of puberty, leading to the development of secondary sexual characteristics before the typical age.

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Type 1 Diabetes Mellitus

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An autoimmune disorder where the pancreas produces little to no insulin, leading to high blood glucose levels.

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Congenital Hypothyroidism

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A deficiency of thyroid hormone at birth, potentially leading to impaired growth and mental development if untreated.

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Klinefelter Syndrome

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A genetic disorder in males where there is an extra X chromosome, leading to hypogonadism and infertility.

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Cushing Syndrome

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A condition caused by excessive levels of cortisol, either from endogenous sources or corticosteroid medications.

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Diabetes Insipidus

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A disorder characterized by an imbalance of fluid in the body, causing extreme thirst and the excretion of large amounts of diluted urine.

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Adrenogenital Syndrome (Congenital Adrenal Hyperplasia)

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Group of genetic disorders affecting the adrenal glands, leading to a deficiency of cortisol and often an excess of androgen hormones.

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Rickets

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A disorder in children caused by vitamin D deficiency, characterized by soft and weak bones.

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Prader-Willi Syndrome

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A genetic disorder resulting in a variety of physical, mental, and behavioral problems. A key feature is a constant sense of hunger that usually begins at about 2 years of age.

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