Search

everythinglearnresearchcommunity

for

Search:↓

Eriocitrin and silymarin might be effective for hair loss treatment and need more research.

The term "Porokeratotic Adnexal Ostial Nevus" is suggested as a more appropriate name.

Proper nutrition can help manage PCOS symptoms and improve overall health.

Some antiseizure medications can cause reversible hair loss, with valproate, lamotrigine, and carbamazepine being the most common.

Testosterone is key for male sexual function, and treating hormone imbalances can improve sexual issues.

Diagnosing and managing Glucocorticoid Resistance Syndrome is complex due to genetic differences and varied symptoms.

Some children in Malaysia with symptoms have either profound or partial biotinidase deficiency, and early testing and treatment are important.

Polycystic Ovary Syndrome (PCOS) in teenagers is a complex condition linked to genetics and environment, often associated with obesity and insulin resistance, and is treated with lifestyle changes and medication.

Women with PCOS are more likely to develop kidney stones, especially those with certain PCOS types.

Hairless protein and putrescine regulate each other, affecting hair growth and skin balance.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

A Korean boy's skin and digestive symptoms were caused by a rare genetic disorder that affects zinc absorption, and he got better with zinc supplements.

NonClassic Congenital Adrenal Hyperplasia is a less severe form of a genetic disorder affecting adrenal gland function.

Nonclassic congenital adrenal hyperplasia is a common genetic disorder that can cause a range of symptoms and requires personalized treatment.

21-hydroxylase deficiency causes hormone imbalances leading to various symptoms, and diagnosis involves clinical and genetic tests.

CTA is often mistaken for AA but doesn't respond to steroids and may require hair transplantation.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

The document concludes that patient outcomes for Congenital Adrenal Hyperplasia are often not ideal because of poor management and a need for better diagnosis and treatment methods.

Cantu syndrome, which causes excessive hair growth and skin issues, is due to a mutation in the ABCC9 gene, and understanding this could help develop new treatments for hair diseases.

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

A Holstein calf in Iran with a severe genetic skin disorder was euthanized due to incurable symptoms.

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.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

Non-classic congenital adrenal hyperplasia is a common disorder causing symptoms like acne and infertility, and it's managed based on symptoms, not just test results. Treatment can improve fertility and reduce miscarriage risk.

Hirsutism is mainly caused by high androgen levels or sensitivity, with PCOS being the most common cause.

Trichoscopy helps accurately diagnose Netherton syndrome, often mistaken for atopic dermatitis.

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

The book explains how excess male hormones can affect various conditions like Polycystic Ovary Syndrome and Cushing's disease.

The skin condition Ulerythema ophryogenes did not improve with treatment in a patient with other birth defects.