Ace The Pediatric Endocrinology Clerkship Exam

Infancy is a period of rapid growth second only to the fetal period. There is a pressing need to optimize nutrition to ensure adequate growth ...

Achondroplasia is a rare genetic disorder recognized as the most common primary skeletal dysplasia in humans. This form of dysplasia accounts for g ...

Luteinizing hormone (LH) is a glycoprotein hormone secreted from the pituitary gland in response to the pulsatile release of gonadotropin-releasing ...

Pancrelipase, which is a combination of lipase, protease, and amylase, has been shown to benefit patients with exocrine pancreatic insufficiency.

Hormone replacement therapy (HRT) is supplementing women with hormones lost during the menopausal transition. To relieve the symptoms associated wi ...

Micropenis is an objective diagnosis made based on the meticulous measurement of the penile length. Given the significant anxiety, stress, and psyc ...

Maple syrup urine disease (MSUD) was first described as a rapid onset of Menkes' neurodegenerative disease in 1954.

There are approximately 29 million people with diabetes in the United States, and approximately 25% of people older the age of 65 have di ...

Fructose 1-phosphate aldolase deficiency or hereditary fruc­tose intol­er­ance (HFI) is an auto­so­mal reces­sive dis­o ...

The adrenal gland is made up of two parts, the cortex and the medulla. The adrenal cortex produces hormones necessary for normal body functioning; ...

Pseudohypoparathyroidism (PHP) is a rare inherited disorder characterized by target organ resistance or unresponsiveness to parathyroid hormone (PT ...

Nonketotic hyperglycinemia is a rare, genetic, inborn error of glycine metabolism. Due to a mutat ...

Klinefelter syndrome (KS) is the result of 2 or more X chromosomes in a phenotypic male. The clinical phenotype of KS was first desc ...

Jacob's syndrome, also known as 47,XYY syndrome, is a rare genetic condition that occurs in about 1 out of 1000 male children. It belongs to a grou ...

Euglycemic DKA (EDKA) is a clinical syndrome occurring both in type 1 (T1DM) or type 2 (T2DM) diabetes mellitus characterized by euglycemia (blood ...

Fructose is a 6 carbon ketonic sugar that is commonly found in a wide variety of foods. Hereditary fructose intolerance is characterized by severe ...

The sex of a fetus is due to the sperm provided by the biological father. Each oocyte, from the biological mother, has an X chromosome and does not ...

Multiple Endocrine Neoplasia Type 1 (MEN1) is a rare endocrine tumor syndrome with high penetrance. This syndrome is also known as Wermer Syndrome. ...