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A genetic marker linked to a type of hair loss was found in most patients studied.

The document concludes that a systematic approach is crucial to identify causes of androgen excess in women beyond the most common cause, Polycystic ovary syndrome (PCOS).

Hair steroid measurement is an effective method to diagnose and monitor CAH in developing countries.

Metreleptin treatment significantly improved metabolic health in a boy with congenital generalized lipodystrophy.

The document explains how to identify different hair problems using a microscope.

The twins' condition is unique and doesn't match any known syndromes.

LC-OCT helps accurately diagnose different types of infant hair loss without invasive methods.

Acne is linked to inflammation and insulin resistance, and is associated with various syndromes that require different treatments.

Up to 50% of scalp hair can be lost before it appears thin, and treatment is only needed for hair loss caused by diseases or deficiencies.

5% topical minoxidil effectively treated a boy's congenital triangular alopecia without side effects.

The document concludes that the girl's hairlessness is likely inherited from her parents.

Men with a certain type of hair loss often use facial moisturizers, and a specific antibiotic treatment may help another hair condition.

Glucocorticoid and mineralocorticoid therapy effectively manage Congenital Adrenal Hyperplasia symptoms but have limitations.

People with reproductive, thyroid disorders, and type 2 diabetes can experience voice changes, but more research is needed to understand this better.

To diagnose Polycystic Ovarian Syndrome, two out of three signs—irregular periods, high male hormone levels, or cysts on the ovaries—are needed.

Topical minoxidil helped an 8-year-old boy with a genetic hair disorder grow hair.

Women with androgen excess, especially those with PCOS, have a much higher risk of heart disease and stroke.

Conditions affecting sex development show that sexual diversity is a natural part of human variation.

The chapter explains that there are many genetic skin disorders affecting skin cell formation, including both common and rare types.

A 21-year-old male with a rare genetic disorder experienced sudden hair loss and high DHEAS levels, likely due to a condition similar to PCOS, usually seen in women.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

A 3-year-old girl with skin mast cell buildup and congenital baldness improved with treatment, suggesting a rare link between these conditions.

Micro-CT helps identify suitable areas for surgical procedures based on blood vessel distribution in hypospadias-affected rats.

Hair loss can have various causes and treatments vary in effectiveness.

Women with congenital adrenal hyperplasia (CAH) have more sexual function issues than those with polycystic ovary syndrome (PCOS), but physical activity can improve sexual functioning in all women.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

Women with nonclassic congenital adrenal hyperplasia experience more sexual dysfunction and distress.

Congenital triangular alopecia is more common than thought and some treatments can be beneficial for appearance concerns.

A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.