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The document says hair loss can happen after recovering from COVID-19 and it can cause psychological discomfort.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

HVDRR is caused by VDR gene mutations, leading to vitamin D resistance, treatable with high calcium doses, but alopecia remains permanent.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

Prolactin levels and gene polymorphism are not linked to vitiligo severity but are related to BMI.

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

Mutations in the AR gene cause hair thinning and loss.

The document suggests changing medical education to balance generalists and specialists, focusing on patient needs.

PCOS is a complex disorder managed by treating symptoms and requires a team of specialists.

The document concludes that periocular hair disorders have various causes and treatments, and proper evaluation by specialists is important for management and prognosis.

The document concludes that managing non-classical congenital adrenal hyperplasia in females requires personalized treatment, genetic counseling, and a team of specialists.

The meeting presented new findings on hair stem cells, pigmentation, genetics, and modern hair treatment techniques.

848 genes related to fat and metabolism are less active in people with Central Centrifugal Cicatricial Alopecia.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

Hair transplantation techniques have improved over 12 years, with follicular unit grafting providing more natural results and potential future advances in automation and genetics.

Some domesticated animals have the same genetic skin diseases as humans, which can help doctors understand human genetic mutations.

Keloid skin disorder involves abnormal fibroblast activation and immune response, linked to a group of genes including FGF11.

Obesity increases the risk of skin infections, inflammatory conditions, and melanoma, but not basal cell carcinoma.

Tofacitinib, a JAK inhibitor, improved hair regrowth in most patients with severe alopecia areata and had minimal side effects.

An 11-year-old child with total hair loss may have a genetic autoimmune disease, and the outlook for hair regrowth is not good.

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.

Early onset hair loss linked to genetics and androgen levels.

The document concludes that combination therapy is most effective for treating excessive hair growth in women with idiopathic hirsutism, and more research is needed to understand the condition.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Ectodermal dysplasia causes various symptoms and early treatment is important for eye, dental, and skin issues.

The symposium highlighted the importance of understanding disease mechanisms for targeted dermatology treatments.

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

Adult acne is often related to hormonal disorders, especially in women, and may need long-term treatment involving specialists.

Insulin resistance contributes to hormone imbalances in many women with polycystic ovary syndrome.