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A woman's nail separation was likely caused by poor blood flow, and a treatment for similar conditions might help.

The cornified envelope is crucial for skin's barrier function and involves key proteins and genetic factors.

The document concludes that correct diagnosis and management of PCOS are important, and more research is needed on its risks and treatments.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

Estrogen and prolactin may play bigger roles in female hair loss than previously thought.

Vitamin D is crucial for skin health and managing skin diseases.

Early hair loss in men and women may indicate a higher risk of heart disease and metabolic problems.

Antifungal treatment can improve severe skin infections with cutaneous horns.

Matriptase is highly active in hair follicles and sebaceous glands, especially during hair growth phases.

The meeting discussed vitamin D3's role in fighting tuberculosis, potential treatments for skin conditions like psoriasis, and hair follicle regeneration as a possible solution for hair loss.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

Melanoma risk tools need improvement, a gene mutation causes a hair disorder that might be treated by managing cell stress, a potential therapy for a skin-ear disorder involves blocking cell channels, skin wrinkling may indicate lung aging regardless of smoking, and oxidative stress might contribute to common baldness.

The vitamin D receptor helps regulate skin and hair health independently of its usual vitamin D ligand.

The TRPV3 ion channel is important for skin and hair health and could be a target for treating skin conditions.

The document concludes that early diagnosis and treatment of Congenital Adrenal Hyperplasia are crucial for preventing serious health issues and improving patient outcomes.

Mutations in the P2RY5 gene cause hereditary woolly hair.

Hirsutism in women often indicates a hormonal imbalance and can be managed with a combination of hormonal treatments and hair removal methods.

A 72-year-old man was diagnosed with a rare skin form of Rosai-Dorfman disease after years of misdiagnosis.

Hirsutism causes significant psychological distress in women.

Hirsutism is too much hair growth in women like the pattern in men, often caused by high male hormones, and can be treated with hormone control and hair removal methods.

A cross-bred lamb with severe skin and movement issues had ichthyosis fetalis but normal vitamin A levels.

Most women with excess hair growth have an underlying hormonal issue, often treated with medication and hair removal methods.

Alopecia areata is likely an autoimmune disease with unclear triggers, involving various immune cells and molecules, and currently has no cure.

New treatments for immune disorders caused by FOXN1 deficiency are promising.

A 2-year-old boy with a rare brain malformation may have Gomez–López-Hernández syndrome.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

Nanostructured delivery systems could potentially improve hair loss treatment by targeting drugs to hair follicles, reducing side effects and dosage, but the best size, charge, and materials for these systems need further investigation.

A young man with an eating disorder had a life-threatening adrenal crisis due to an autoimmune condition, highlighting the need for better education on managing hormone treatments.

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

Men with early hair loss may have a higher risk of enlarged prostate and possibly prostate cancer due to shared hormonal factors.