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The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

New treatments targeting the Hedgehog pathway can help treat advanced skin cancer but may have side effects and their effectiveness in early stages is unknown.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

Woodhouse-Sakati syndrome shows varied symptoms, including hair loss and diabetes, and is common in Qatar due to a specific genetic variant.

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

Akt2 protein is essential for normal cell division in early mouse embryos.

The document concludes that hair analysis is not good for assessing nutrition but can detect long-term heavy metal exposure.

New acne treatments include combination creams, advanced retinoids, and light therapies, focusing on safety and patient adherence.

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

Three dogs with a rare skin condition improved with treatment.

Frontal Fibrosing Alopecia needs better diagnostics and treatments, with dutasteride showing promise.

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

Telogen Effluvium is a common hair loss condition that can be short-term or long-lasting and is often caused by stress, illness, or nutritional issues.

Lipase H is important for hair follicle function and shaping hair fibers.

Adult female acne is a complex condition that can worsen with menopause, requiring holistic treatment and tailored skincare at different life stages.

PCOS may increase the risk of certain cancers.

New technologies show promise in healing wounds, treating cancer, autoimmune diseases, and genetic disorders.

PCOS is a hormonal disorder causing symptoms like irregular periods and acne, and increases the risk of diabetes and heart disease.

Up to half of adult women may experience hair loss, and doctors should use medical history, exams, and tests to find the cause and treat it.

Fat-related cells are important for initiating hair growth.

Half of people with Alopecia Areata may see hair regrowth within a year without treatment, but recovery is unpredictable.

Childhood obesity is rising globally due to various factors, and early prevention and healthy lifestyle changes are crucial.

Wnt1/βcatenin signaling is crucial for heart repair after injury.

The timing of when the gene Bmal1 is active affects aging and survival, with its absence during development, not adulthood, leading to premature aging.

Epidermal stem cells are diverse and vary in activity, playing key roles in skin maintenance and repair.

The update highlights that non-classic congenital adrenal hyperplasia is common in women with excess male hormones, requires specific hormone tests for diagnosis, and has various treatment options depending on age and symptoms.

New treatments targeting specific genes show promise for treating keratin disorders.

Pregnancy can cause skin pigmentation, stretch marks, and changes in hair, nails, and sweat glands, with most resolving after birth.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

PCOS affects women's health by increasing the risk of diabetes, heart disease, and reproductive issues.