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A patch with curcumin-zinc can improve hair growth and health by delivering beneficial particles to the skin, increasing hair follicles, and reversing effects of a hair loss hormone.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

People with depression often have higher hair cortisol levels, while those with PTSD tend to have lower levels, but more research is needed to understand this fully.

The Lanceolate hair-J mutation in mice mimics human hair disorders like Netherton's syndrome.

The report shows a young man with Hutchinson-Gilford Progeria Syndrome had typical and additional eye problems related to the disease.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

Agouti and AGRP affect pigmentation and obesity, with implications for metabolic disorders.

A man's scalp hair loss was due to a combined melanocytic nevus and alopecia areata, suggesting a possible link between the two conditions.

Minoxidil base is preferred for hair loss treatment, but minoxidil sulfate may be an alternative for unresponsive patients.

Blocking certain receptors in the lungs might help treat a specific type of asthma.

A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

TAGX-0003 protected hair follicles and reversed alopecia areata in a mouse model.

SCD-153 shows promise as an effective topical treatment for alopecia areata.

A rare case showed hair regrowth after chemotherapy for thymoma, suggesting a link between alopecia areata and thymoma.

Majocchi's granuloma can occur in kidney transplant patients on tacrolimus and can be treated with antifungal medication.

Melasma results from changes in the skin's pigment and structure, not just pigment cell growth.

A woman with a rare form of multiple myeloma had a headache and a skull mass, which led to her diagnosis after tests and a biopsy.

TGFα gene mutation in mice causes abnormal skin, wavy hair, curly whiskers, and sometimes eye inflammation.

Early diagnosis and treatment of hereditary hemochromatosis can prevent serious complications.

The gene for Marie Unna hereditary hypotrichosis is located on chromosome 8p21.

The term "low-risk" in myelodysplastic syndrome is misleading and should be changed to better reflect patient experiences and needs.

The hairless gene is crucial for hair health, and its mutations cause hair loss.

A mutation in mice causes hair loss and skin issues due to a defect in a gene affecting cell adhesion.

MEK and BRAF inhibitors increase sebum production and accumulation, which could cause acne-like side effects.

Follicular mycosis fungoides can look like a B-cell lymphoma, making diagnosis difficult.

Hair testing can detect a single GHB exposure, useful for documenting sexual assault.

Mice with human-like EGFR had growth issues, skin defects, heart problems, and unusual bone development.

A man with alopecia universalis regrew hair temporarily after a bone treatment.

A dissolving microneedle patch with collagen XVII effectively promotes hair regrowth in androgenic alopecia.