Search

everythinglearnresearchcommunity

for

Search:↓

Testing for CAG repeat polymorphism in the androgen receptor gene is not currently recommended for managing hypogonadism.

TTD hair brittleness is caused by multiple structural abnormalities.

Biotin and acetazolamide improved hair and nail growth, mental function, and reduced headaches in a child with autism.

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

The document reports three sisters with Woodhouse-Sakati syndrome showing typical symptoms and unusual gynecological anomalies.

The cause and importance of misplaced oil glands in the hair follicle are not well understood.

Oral isotretinoin temporarily improved skin symptoms in a child with IFAP syndrome.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

IL-36α helps grow new hair follicles and speeds up wound healing.

The document concludes that proper diagnosis and treatment of hair shaft disorders require understanding their unique causes and avoiding hair-damaging practices.

Adrenal disorders can cause lasting brain and behavior issues in children.

The document explains the genetic causes and characteristics of inherited hair disorders.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

Understanding skin structure and development helps diagnose and treat skin disorders.

Non-coding RNAs are important for hair growth and could lead to new hair loss treatments, but more research is needed.

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

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

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

The guideline recommends mental health involvement in diagnosing gender identity disorder and outlines hormone and surgical treatment protocols, emphasizing safety, informed consent, and long-term monitoring.

Taking riboflavin and eating less lysine can help some people with a specific genetic disorder avoid brain damage.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

Hairless protein is crucial for healthy skin and hair, and its malfunction can cause hair loss.

Researchers created rat liver stem cells that could help repair liver failure in rats and may be useful for studying human liver diseases.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

Most hair loss in children is caused by a few common conditions, and it's important to diagnose these properly and support the child's mental health.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

Small hormonal imbalances can cause significant health problems, so more sensitive testing for hormone-disrupting chemicals is needed.

A family was found with both Trichorhinophalangeal syndrome and Loose Anagen Syndrome, suggesting a genetic connection.

Six genetic conditions are often linked to complete scalp hair loss in children.

Certain groups may need vitamin supplements to improve hair health and prevent other health problems.