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Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

A 23-year-old Syrian woman has two rare hair disorders, and avoiding hair treatments plus using vitamins and minoxidil may help.

Excessive hair loss can be an early sign of celiac disease.

The COVID-19 pandemic did not significantly change stress levels in preschoolers, but higher-income families' children showed higher stress.

L-PGDS has specific binding sites for its functions and could help in drug delivery system design.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

A new gene, mrp4, is found in mice and may play a unique role in hair follicle development in tails and ears.

Keratin 26 affects cashmere goat hair growth and is influenced by various treatments.

Many young women have Polycystic Ovarian Syndrome (PCOS), which is often linked with irregular periods, depression, low self-esteem, and insomnia. Lifestyle and diet changes, along with regular counseling, can help manage these symptoms.

Certain types of alopecia areata are linked to allergies, autoimmune diseases, and family history.

The Polish medical societies have redefined metabolic syndrome and recommend lifestyle changes, certain medications, and possibly bariatric surgery for treatment. They also discuss managing related health conditions.

Chinese men have lower AGA rates than Caucasians, with type III vertex most common; family history is important.

Children with alopecia areata should only have thyroid screening if they have Down syndrome, a history of atopy, family history of thyroid disease, or signs of thyroid problems.

Premature hair graying in young Turkish adults is more likely if they have stress, a family history of graying, drink alcohol, have chronic diseases, are older, or are taller.

The conclusion is that in the Indian subcontinent, socioeconomic status, stress, and family structure affect the severity of alopecia areata, and its psychological impact is generally mild or moderate.

Most people in Turkey start getting gray hair around 33 years old, with factors like age, education, hair loss, skin type, family history, and anxiety playing a role.

Men with sleep apnea and low iron levels are more likely to have male-pattern baldness, especially if they have a family history of hair loss.

Family-based treatment is the best outpatient care for stable teens with anorexia, and more research is needed on medication and treatment effectiveness for young people with eating disorders.

People with a family history of hair loss are more likely to experience it, and the severity of hair loss is linked to insulin resistance. The connection between early hair loss and oxidative stress needs more investigation.

Over half of young people in Saudi Arabia experience early gray hair, linked to factors like smoking, stress, and family history.

There's a significant link between the severity of Seborrheic Dermatitis and the pattern of hair loss in people with a family history of hair loss.

Testosterone therapy in transgender men can lead to hair loss, with the risk increasing over time and influenced by family history.

Older, overweight women with children and a family history of hair loss are more likely to experience female pattern hair loss.

Family caregivers take longer to fall asleep and have more sleep disturbances, which may contribute to their health problems.

Family history and stress are linked to early hair graying, with family history being the main factor.

Family history affects onset and severity of androgenic alopecia, but treatment success depends more on therapy duration.

Androgenetic alopecia is more common in Indian men than women, and family history is a strong risk factor.