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A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Hair loss in certain young mice is linked to a specific gene and can be caused by lack of iron.

Genetics, stress, and health issues can cause early hair greying, which affects self-esteem, and there's no cure, only hair dye.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

The document concludes that hair curvature can be explained by the growth patterns caused by the shape and separation of cells in the hair follicle and is affected by specific molecular pathways.

A 12-year-old girl's hair loss was linked to a rare genetic condition called ALX4-related frontonasal dysplasia.

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

A boy's hair that was frizzy and hard to comb returned to normal after 9 months, possibly due to genetic factors.

Different causes of beard hair loss have various treatments, including medications, lifestyle changes, and procedures to stimulate hair growth.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

PCOS is often caused by hormonal imbalances that can lead to various health issues and may indicate a risk for future metabolic and cardiovascular problems.

Ovulation disorders are a major cause of infertility and menstrual problems in women.

Diuretics can cause serious side effects and should be used carefully.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

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 individuals with a rare genetic disorder linked to the AEBP1 gene may experience a unique type of hair loss and should be monitored for heart issues.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

A one-year-old child with a genetic condition had symptoms improved by treating zinc deficiency.

The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

The document covers various male health issues, their causes, treatments, and related conditions.

Cicatricial alopecia, a permanent hair loss condition, is mainly caused by damage to specific hair follicle stem cells and abnormal immune responses, with gene regulator PPAR-y and lipid metabolism disorders playing significant roles.

The document concludes that early recognition and treatment of PCOS in adolescents is crucial for managing symptoms and long-term health risks.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

Hair shaft disorders, often due to genetics or environment, lack specific treatments but can be managed with gentle hair care and may improve with age or topical treatments.

Effective treatments for spinal and bulbar muscular atrophy are not yet available; more research is needed.

Arab APS1 patients have unique and recurrent AIRE gene mutations.

New treatments and diagnostic methods for various animal skin conditions showed promising results.

Certain gene mutations can weaken the skin barrier and, when combined with environmental factors, lead to eczema and severe itching.

The genes KRT25 and SP6 affect curly hair in horses, with KRT25 also causing hair loss. If both genes are mutated, the horse gets curly hair and hair loss. KRT25 can hide the effect of SP6.