USMLE® Step 1 style questions USMLE
USMLE® Step 2 style questions USMLE
A 16-year-old boy comes to the clinic because of a lack of sexual development. All of his friends have gone through puberty and he is embarrassed by his young appearance. His temperature is 37.0°C (98.6°F), pulse is 76/min, respirations are 12/min, and blood pressure is 121/76 mm Hg. Physical examination shows Tanner stage 1 development of the genitals and pubic hair. Neurologic examination shows an inability to identify different smells. Laboratory studies show decreased testosterone and luteinizing hormone. Which of the following is the most likely diagnosis?
Kallmann syndrome is an endocrine disorder caused by a decrease in sex hormones, either testosterone in males or estrogen and progesterone in females. That decrease leads to a failure to start or complete puberty.
The syndrome is named after Dr. Franz Kallmann, the geneticist who first described it.
Normally, during fetal development there’s a region of the brain called the olfactory placode. Two groups of neurons emerge from that region.
The first group contains olfactory neurons that eventually help with sensing smells.
These neurons migrate down from the olfactory placode and get embedded in the cribriform plate, which is a bone plate that separates the nasal cavity from the brain, forming the olfactory bulb.
The second group contains neurons that release gonadotropin-releasing hormone.
And these neurons migrate through the cribriform plate, and settle in the hypothalamus.
The hypothalamic-pituitary-gonadal axis is a system of hormone signaling between the hypothalamus, pituitary gland, and gonads, either the testes or ovaries, to control sexual development and reproduction.
When gonadotropin-releasing hormone reaches the pituitary gland, it stimulates cells in the anterior pituitary, called gonadotrophs, to release gonadotropin hormones, luteinizing hormone and follicle-stimulating hormone into the blood.
These gonadotropin hormones then stimulate the gonads to produce sex specific hormones.
In females, the theca cells respond to luteinizing hormone by producing progesterone and androstenedione.
Then, follicle stimulating hormone causes the granulosa cells to convert the androstenedione into estrogen.
During puberty, waves of estrogen and progesterone regulate primary sex characteristics, like monthly changes to the ovary stroma to promote egg maturation and ovulation, and changes to the uterine wall lining as part of the menstrual cycle.
They also direct secondary sex characteristic development like increased height, growth of pubic hair and breasts.
- "Robbins Basic Pathology" Elsevier (2017)
- "Harrison's Principles of Internal Medicine, Twentieth Edition (Vol.1 & Vol.2)" McGraw-Hill Education / Medical (2018)
- "Pathophysiology of Disease: An Introduction to Clinical Medicine 8E" McGraw-Hill Education / Medical (2018)
- "CURRENT Medical Diagnosis and Treatment 2020" McGraw-Hill Education / Medical (2019)
- "Harrison's Endocrinology, 4E" McGraw-Hill Education / Medical (2016)
- "Clinical Genetic Testing for Kallmann Syndrome" The Journal of Clinical Endocrinology & Metabolism (2013)
- "Congenital Hypogonadotropic Hypogonadism and Kallmann Syndrome: Past, Present, and Future" Endocrinology and Metabolism (2015)