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Fox Fordyce disease can occur in prepubertal girls and may be underdiagnosed.

Certain genes are more active in baby scalp cells and can help grow hair when added to adult mouse skin cells.

Adult stem cells with Tp63 can form hair and skin cells when placed in new skin, showing they have hidden abilities for skin repair.

Operative hysteroscopy is still the main treatment for Asherman syndrome, but more research is needed on post-surgery methods.

Finasteride affects SRD5A2 gene pattern, possibly causing lasting side effects.

Some children with localized scleroderma are rarely resistant to methotrexate, and no common profile for resistance was found.

FFA in men, often mistaken for other hair loss types, may be more common than thought and needs larger studies for confirmation.

A woman with anorexia improved significantly after being treated for scurvy with vitamin C, despite not showing typical scurvy symptoms.

Effective symptom management in IBD improves quality of life and prevents complications.

Modified stem cells that overexpress a specific protein can improve hair growth and reduce hair abnormalities in mice.

New treatments for skin conditions in children include a preferred drug for birthmark reduction, proactive creams for eczema and vitiligo, a safe psoriasis medication, and special tissues and socks for eczema and fungal infections.

Both ASR I and ASR II are effective scalp reduction techniques, with ASR I creating finer scars and ASR II removing more bald area and reducing stretch-back.

A woman had a skin reaction from a cough suppressant, dextromethorphan, which is a new cause of fixed-drug eruption.

Current research explores hair growth drugs, while future research aims for personalized treatments.

Different cell types work together to repair skin, and targeting them may improve healing and reduce scarring.

Finasteride for hair loss may cause lasting sexual, genitourinary, mental, and anti-androgenic side effects in young men.

Hair tourniquet syndrome in infants can be treated successfully with immediate hair removal.

Researchers found a new early sign of Frontal Fibrosing Alopecia that could help avoid misdiagnosis.

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

Several new treatments for different types of hair loss show promise in improving patient quality of life.

Sardinians were historically short due to a mix of genetics and factors like disease and poor nutrition, but recent height increases suggest better living conditions had a bigger impact.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

Keratin hydrogel from human hair helps rats recover better from spinal cord injuries.

Some skin medications are safe for pregnant women, but others pose risks or should not be used.

The mini-lift is a less invasive face-lift for younger patients that is quicker, cheaper, and has a fast recovery, but is less effective for the midface and excessive neck skin.

The document concludes that periocular hair disorders have various causes and treatments, and proper evaluation by specialists is important for management and prognosis.

A hair tightly wrapped around a toddler's toe caused severe crying and was treated by surgery.

Two mouse mutations cause similar hair loss despite different skin changes.

Stress may affect hair growth by influencing hair follicle development and could contribute to hair loss.