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Epidermolysis bullosa is an inherited condition causing fragile skin with no cure, managed by wound care and experimental treatments show promise.

The symposium highlighted the importance of genetics in understanding and treating complex skin diseases.

Multi-omics techniques help understand the molecular causes of androgenetic alopecia.

Oral minoxidil and growth factors improved hair density and thickness in a girl with hereditary hair loss.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.

Increased FGFR2b signaling, influenced by androgens, plays a role in causing acne.

Genetic variations greatly affect individual metabolism and can impact health and disease risk.

Claudin expression changes help the skin respond to injury.

Some children in Malaysia with symptoms have either profound or partial biotinidase deficiency, and early testing and treatment are important.

Accurate diagnosis of APL is crucial to avoid unnecessary treatments.

Research from 2011 to 2020 shows androgen receptors could be key for prognosis and treatment in certain breast cancers.

TRPV4 helps cells repair tissue and reduce scarring by controlling calcium levels.

Early diagnosis and genetic evaluation of ADULT syndrome are crucial to reduce stress and medical costs.

Docetaxel often causes hair loss, with limited effective treatments and no cure for permanent hair loss.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

Delta-opioid receptors affect skin cell circadian rhythms, possibly impacting wound healing and cancer.

The review shows that skin symptoms like chronic fungal infections, hair loss, and skin depigmentation are key for early detection and management of APECED.

Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.

A child with Olmsted syndrome showed mild improvement in hair and skin issues with treatment.

The document concludes that more local research on African skin and hair is needed despite increased scientific output from Sub-Saharan Africa.

Rare genetic variants in five specific genes are linked to male-pattern hair loss but only account for a small part of the risk.

The research found new potential mechanisms in mouse hair growth by studying RNA interactions.

Researchers found genes linked to hair growth cycles in Inner Mongolia cashmere goats, which could help understand and treat hair loss.

The document concludes that hair loss and acne in women can be due to both androgen-related and unrelated causes, requiring a collaborative treatment approach.

Vitamin D receptor helps control hair growth and could be used to treat certain skin tumors.

Gardenia florida fruit extract may help hair grow and needs more research to understand how.

EAAT4 decreases with age, harming skin function and calcium balance.

Understanding wool keratin-associated proteins in sheep can help improve wool quality through selective breeding.

PPARγ is essential for maintaining healthy skin, controlling inflammation, and ensuring proper skin barrier function.

Researchers identified five new potential targets for leishmaniasis treatment, suggesting repurposing existing drugs could be effective.