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Mutations in the NR3C1 gene cause a rare condition that affects hormone signaling and can lead to various symptoms, with dexamethasone as a treatment option.

A rare fungal infection on a child's scalp was successfully treated with antifungal medication.

Researchers found a gene mutation responsible for a rare hair loss condition.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

An 80-year-old man's deep beard infection was cured with oral terbinafine after identifying the fungus Trichophyton verrucosum.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

The near-naked hairless mutation causes hair loss but is not due to a mutation in the hairless gene itself.

Porphyra-334 may help reduce wrinkles and promote hair growth.

Key genes can rewire networks, changing skin appendage types.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

The gene URB is more active in human hair growth cells and responds to a hair-related hormone.

New research shows that skin diversity is influenced by different types of dermal fibroblasts and their development, especially involving the Wnt/β-catenin pathway.

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

A specific gene mutation causes long hair in Angora rabbits.

BMI1 is essential for preventing hair greying and maintaining hair color.

ELL is crucial for gene transcription related to skin cell growth.

A young cat had a rare fungal infection caused by Microsporum gypseum.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

The document concludes that specific hair and blood vessel abnormalities in infants with seizures and developmental issues may indicate Menkes disease, which lacks a cure and is often fatal by age 3.

Minoxidil may help reduce aging effects in brain cells.

The symposium highlighted the importance of understanding disease mechanisms for targeted dermatology treatments.

Malassezia yeast plays a key role in dandruff and seborrhoeic dermatitis.

Lipids may help treat hair loss by promoting hair growth through the HIF-1 pathway.

Exosomes help hair follicle development in cashmere goats.

CGF therapy may effectively treat psoriasis by reducing inflammation.

Ayme-Gripp Syndrome was confirmed in a woman through genetic testing, highlighting the need to consider rare genetic conditions in diagnoses.

NIMO-CH hydrogel effectively heals wounds with minimal scarring and promotes hair growth.

Type 1 Diabetes prevents hair growth by causing cell death in hair follicles.